Patent Application
20120202801
Methods for treating breast cancer involving the administration of a compound that selectively inhibits pathological production of human vascular endothelial growth factor (VEGF) are described. The compound can be administered as a single agent therapy or in combination with one or more additional therapies to a human in need of such treatment.
Breast cancer is characterized by the growth of malignant cells in the mammary glands. Worldwide, breast cancer is the second most common type of cancer and the fifth most common cause of cancer death, causing 519,000 deaths worldwide in 2004 (see, “Fact Sheet No. 297: Cancer”, World Health Organization, February 2006). Among women in the United States, breast cancer is the most common cancer and the second most common cause of cancer death (see Espey et al., 2007, Cancer, 110(10): 2119-52). Women in the United States have a 1 in 8 lifetime chance of developing invasive breast cancer and a 1 in 35 chance of breast cancer causing their death (see Espey et al., 2007, Cancer, 110(10): 2119-52).
The first symptom, or subjective sign, of breast cancer is typically a lump that feels different from the surrounding breast tissue. Indications of breast cancer other than a lump may include changes in breast size or shape, skin dimpling, nipple inversion, or spontaneous single-nipple discharge. The first objective indication of breast cancer as detected by a physician, is discovered by mammography, which is the process of using low-dose amplitude X-rays to examine the human breast tissue. Occasionally, breast cancer presents as metastatic, wherein the cancer that has spread beyond the breast tissue. Common sites of metastasis include bone, liver, lung and brain. No etiology is known for 95% of breast cancer cases, while approximately 5% of new breast cancers are attributable to hereditary syndromes. In particular, carriers of the breast cancer susceptibility genes, BRCA1 and BRAC2, are at a 30-40% increased risk for breast cancer.
For patients presenting with confined local-regional breast cancer (Stage 1, II, or HA), the development of systemic hormonal and cytotoxic therapies as adjuvants to primary surgery and breast irradiation have substantially improved outcomes by delaying recurrence of disease. However, for patients who present with large or inflammatory primary tumors or metastases (Stage IIIB-C, IV), or who develop recurrent metastatic disease, breast cancer becomes a life-threatening disorder. Systemic therapy for patients with advanced breast cancer has focused on sequential use of systemic treatments to impede the disease progression that leads to disabling symptoms and death (see Carlson et al., 2005, Update: NCCN breast cancer Clinical Practice Guidelines, J Natl Compr Canc Netw, Suppl 1:S7-11). Post-menopausal patients with hormone-receptor-positive tumors are usually offered treatment to block estrogenic pathways; such therapy is initiated first since it is relatively nontoxic and can be delivered orally. Given evidence of improved tumor control, use of aromatase inhibitors (e.g., exemestane, anastrozole, letrozole) to block estrogen production within tumors and other tissues are increasingly used as an alternative to estrogen receptor blockage with tamoxifen (see Joensuu et al., 2005, Acta Oncol., 44(1):23-31). Upon disease progression, cytotoxic chemotherapy in various sequences and combinations is administered. In 2005, the most commonly used agents approved by the Food and Drug Administration (FDA) include taxanes (e.g., paclitaxel, docetaxel) and nucleoside analogues (e.g., capecitabine, gemcitabine), although older agents such as anthracyclines (e.g., doxorubicin, epirubicin), alkylators (e.g., cyclophosphamide, melphalan), and platins (e.g., cisplatin, carboplatin) are still employed (see Carlson et al., 2005, Update: NCCN breast cancer Clinical Practice Guidelines, J Natl Compr Canc Netw, Suppl 1:S7-11). For the 25% of breast cancer patients with tumors in which HER2 is amplified, treatment with anti-HER2 antibody, tastuzumab, is often added to cytotoxic treatment. In 2008, bevacizumab, an anti-VEGF antibody, was approved by the FDA to be used in combination with paclitaxel in patients with metastatic breast cancer (see Miller et al., 2007, N Engl J. Med. 357(26): 2666-76).
The development of newer agents in the past decade illustrates that it is still possible to improve care by offering more efficacious, less toxic, and more convenient options to patients with advanced breast cancer. However, despite these advancements, the 5-year survival rate for patients with metastatic breast cancer remains less that 30% and tumor progression still causes the death of 41,000 women per year in the United States (see Smigal et al., 2006, Trends in breast cancer by race and ethnicity: update 2006, Cancer J. Clin., 56(3):168-83). These facts emphasize the continued need for translation of new approaches into therapies for patients with this life-threatening malignancy.
Methods for treating breast cancer are described involving the administration of compounds having the formulas set forth herein (“Compound”) to a human subject in need of such treatment. Preferably, the Compound used in the therapeutic method demonstrates one or more of the following activities as determined in cell culture and/or animal model systems, such as those described herein: (a) selective inhibition of the pathological production of human VEGF; (b) inhibition of tumor angiogenesis, tumor-related inflammation, tumor-related edema, and/or tumor growth; and/or (c) prolongation of the G1/S phase of cell cycle.
The Compound can be administered as a single agent therapy to a human in need of such treatment. Alternatively, the Compound can be administered in combination with one or more additional therapies to a human in need of such treatment. Such therapies may include the use of anti-cancer agents (e.g., cytotoxic agents, anti-angiogenesis agents, tyrosine kinase inhibitors or other enzyme inhibitors).
While not bound by any theory, the therapies described are based, in part, on the pharmacodynamic activities of the Compounds as measured in cell culture and in animal models; in particular, these include: (a) selective inhibition of the pathological production of human VEGF; (b) inhibition of tumor angiogenesis, tumor-related inflammation, tumor-related edema and/or tumor growth; and/or (c) prolongation of the G1/S phase of the cell cycle of tumor cells.
These pharmacologic activities contribute to limiting solid tumor growth, tumor-related inflammation and/or tumor-related edema in several ways. For example, inhibition of pathological production of human VEGF by the tumor will inhibit tumor angiogenesis, thereby limiting vascularization and further growth of solid tumors. An additional benefit is achieved for tumors that respond to VEGF as a growth factor—in such cases, the Compound can limit proliferation of such tumor cells independent of their angiogenic status, that is angiogenesis and vascularization need not be present for the Compound to limit proliferation of the tumor cells. Because the process of tumorigenesis can result in inflammation and edema, a Compound may limit such inflammation or edema. Finally, the prolongation of cell cycle may contribute to the induction of apoptotic death of the tumor cells, and/or allow for increased efficacy when the Compound is used in combination with a therapy or therapies (e.g., chemotherapeutic agents or radiation) that interfere with nucleic acid synthesis during the cell cycle (e.g., the G1/S phase).
Thus, in specific embodiments, the methods for treating breast cancer can result in inhibition or reduction of the pathological production of human VEGF (including intratumoral VEGF production), thus reducing human VEGF concentrations in biological specimens of an afflicted subject; inhibition of tumor angiogenesis, tumor-related inflammation, tumor-related edema, and/or tumor growth in the subject; stabilization or reduction of tumor volume or tumor burden in the subject; stabilization or reduction of peritumoral inflammation or edema in the subject; reduction of the concentration of angiogenic or inflammatory mediators in biological specimens (e.g., plasma, serum, cerebral spinal fluid, urine or any other biofluids) from the subject; and/or a delayed or prolonged G1/S phase of the cell cycle (i.e., the period between the late resting or pre-DNA synthesis phase, and the early DNA synthesis phase) in tumor cells of the subject.
Existing antiangiogenic therapies have been developed for other diseases (e.g., certain cancers, retinopathies including macular degeneration and the like) are directed at neutralizing VEGF activity (e.g., using anti-VEGF antibodies), or inhibiting downstream effects of VEGF signaling (e.g., using tyrosine kinase inhibitors to block the signaling activity of the VEGF receptor). As a result, these existing antiangiogenic therapies neutralize or inhibit physiological or homeostatic VEGF, as well as pathologically produced human VEGF, activity resulting in side effects that, while tolerated for the treatment of life-threatening cancers or to prevent or slow the development of hearing loss or blindness, may not be acceptable for the treatment of breast cancer. Since the Compounds used in the therapeutic methods described herein selectively inhibit pathologic production of human VEGF (e.g., by the tumor), and do not disturb the production of human VEGF under physiological conditions, side effects that are unacceptable for the treatment of breast cancer should be reduced.
The efficacy of the therapeutic intervention is supported by the data presented herein, demonstrating that: the Compounds inhibit the pathological production of human VEGF (see Section 9.1 et. seq., infra); the Compounds inhibit tumor angiogenesis and tumor growth (see Section 9.2 et. seq., infra); the Compounds delay cell cycle by prolonging the G1/S phase (see Section 9.3 et. seq., infra); the Compounds can be administered safely to human subjects (see Section 10.2 et. seq., infra); and the Compounds inhibit the growth of xenograft human breast cancer tumors in animal model systems (see Section 9.2.5 et. seq. and Section 12, infra).
As used herein, the terms “therapies” and “therapy” can refer to any protocol(s), method(s), compositions, formulations, and/or agent(s) that can be used in the prevention, treatment, management, or amelioration of a condition or disorder or symptom thereof (e.g., cancer or a symptom or condition associated therewith, or breast cancer or a symptom or condition associated therewith). In certain embodiments, the terms “therapies” and “therapy” refer to drug therapy, adjuvant therapy, radiation, surgery, biological therapy, supportive therapy, and/or other therapies useful in treatment, management, prevention, or amelioration of a condition or disorder or a symptom thereof (e.g., cancer or a symptom or condition associated therewith, or breast cancer or a symptom or condition associated therewith). In certain embodiments, the term “therapy” refers to a therapy other than a Compound or pharmaceutical composition thereof. In specific embodiments, an “additional therapy” and “additional therapies” refer to a therapy other than a treatment using a Compound or pharmaceutical composition. In a specific embodiment, a therapy includes the use of a Compound as an adjuvant therapy. For example, using a Compound in conjunction with a drug therapy, biological therapy, surgery and/or supportive therapy.
As used herein, the term “effective amount” in the context of administering a Compound to a subject refers to the amount of a Compound that results in a beneficial or therapeutic effect. In specific embodiments, an “effective amount” of a Compound refers to an amount of a Compound which is sufficient to achieve at least one, two, three, four or more of the following effects: (i) the reduction or amelioration of the severity of one or more symptoms associated with breast cancer; (ii) the reduction in the duration of one or more symptoms associated with breast cancer; (iii) the prevention in the recurrence of a tumor or a symptom associated with breast cancer; (iv) the regression of tumors and/or one or more symptoms associated therewith; (v) the reduction in hospitalization of a subject; (vi) the reduction in hospitalization length; (vii) the increase in the survival of a subject; (viii) the inhibition of the progression of tumors and/or a symptom associated therewith; (ix) the enhancement or improvement of the therapeutic effect of another therapy; (x) a reduction in the growth of a tumor or neoplasm associated with breast cancer; (xi) a decrease in tumor size (e.g., volume or diameter); (xii) a reduction in the formation of a newly formed tumor; (xiii) eradication, removal, or control of primary, regional and/or metastatic tumors associated with breast cancer; (xiv) ease in removal of tumors by reducing vascularization prior to surgery; (xv) a decrease in the number or size of metastases; (xvi) a reduction in mortality; (xvii) an increase in tumor-free survival rate of patients; (xviii) an increase in relapse-free survival; (xix) an increase in the number of patients in remission; (xx) a decrease in hospitalization rate; (xxi) the size of the tumor is maintained and does not increase or increases by less than the increase of a tumor after administration of a standard therapy as measured by conventional methods available to one of skill in the art, such as magnetic resonance imaging (MRI), dynamic contrast-enhanced MRI (DCE-MRI), X-ray (e.g., mammography), computed tomography (CT) scan, a positron emission tomography (PET) scan (e.g., positron emission mammography), or ultrasound; (xxii) the prevention of the development or onset of one or more symptoms associated with breast cancer; (xxiii) an increase in the length of remission in patients; (xxiv) the reduction in the number of symptoms associated with breast cancer; (xxv) an increase in symptom-free survival of breast cancer patients; (xxvi) inhibition or reduction in pathological production of VEGF; (xxvii) stabilization or reduction of peritumoral inflammation or edema in a subject; (xxviii) reduction of the concentration of VEGF or other angiogenic or inflammatory mediators (e.g., cytokines or interleukins) in biological specimens (e.g., plasma, serum, cerebral spinal fluid, urine or any other biofluids); (xxiv) reduction of the concentration of P1GF, VEGF-C, VEGF-D VEGF-R, IL-6 and/or IL-8 in biological specimens (e.g., plasma, serum, cerebral spinal fluid, urine or any other biofluids); (xxv) inhibition or decrease in tumor metabolism or perfusion; (xxxvi) inhibition or decrease in angiogenesis or vascularization; (xxxii) improvement in quality of life as assessed by methods well known in the art. In specific embodiments, an “effective amount” of a Compound refers to an amount of a Compound specified herein in, e.g., section 5.4 below.
Concentrations, amounts, cell counts, percentages and other numerical values may be presented herein in a range format. It is to be understood that such range format is used merely for convenience and brevity and should be interpreted flexibly to include not only the numerical values explicitly recited as the limits of the range but also to include all the individual numerical values or sub-ranges encompassed within that range as if each numerical value and sub-range is explicitly recited.
As used herein, the term “elderly human” refers to a human 65 years or older.
As used herein, the term “human adult” refers to a human that is 18 years or older.
As used herein, the term “human child” refers to a human that is 1 year to 18 years old.
As used herein, the term “subject” and “patient” are used interchangeably to refer to an individual. In a specific embodiment, the individual is a human. See Section 5.3 infra for more information concerning patients treated for breast cancer in accordance with the methods provided herein.
As used herein, the term “pharmaceutically acceptable salt(s)” refers to a salt prepared from a pharmaceutically acceptable non-toxic acid or base including an inorganic acid and base and an organic acid and base. Suitable pharmaceutically acceptable base addition salts of the Compounds provided herein include, but are not limited to metallic salts made from aluminum, calcium, lithium, magnesium, potassium, sodium and zinc or organic salts made from lysine, N,N′-dibenzylethylenediamine, chloroprocaine, choline, diethanolamine, ethylenediamine, meglumine (N-methylglucamine) and procaine. Suitable non-toxic acids include, but are not limited to, inorganic and organic acids such as acetic, alginic, anthranilic, benzenesulfonic, benzoic, camphorsulfonic, citric, ethenesulfonic, formic, fumaric, furoic, galacturonic, gluconic, glucuronic, glutamic, glycolic, hydrobromic, hydrochloric, isethionic, lactic, maleic, malic, mandelic, methanesulfonic, mucic, nitric, pamoic, pantothenic, phenylacetic, phosphoric, propionic, salicylic, stearic, succinic, sulfanilic, sulfuric, tartaric acid, and p-toluenesulfonic acid. Specific non-toxic acids include hydrochloric, hydrobromic, phosphoric, sulfuric, and methanesulfonic acids. Examples of specific salts thus include hydrochloride and mesylate salts. Others are well-known in the art, see for example, Remington's Pharmaceutical Sciences, 18th eds., Mack Publishing, Easton Pa. (1990) or Remington: The Science and Practice of Pharmacy, 19th eds., Mack Publishing, Easton Pa. (1995).
As used herein, the term “alkyl” generally refers to saturated hydrocarbyl radicals of straight or branched configuration including, but not limited to methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, n-hexyl, n-heptyl, octyl, n-octyl, and the like. In some embodiments, alkyl substituents can be C1 to C8, C1 to C6, or C1 to C4 alkyl. Alkyl may be optionally substituted where allowed by available valences, for example, with one or more halogen or alkoxy substituents. For instance, halogen substituted alkyl may be selected from haloalkyl, dihaloalkyl, trihaloalkyl and the like.
As used herein, the term “cycloalkyl” generally refers to a saturated or partially unsaturated non-aromatic carbocyclic ring. Representative examples of cycloalkyl include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclopentadienyl, cyclohexyl, cyclohexenyl, 1,3-cyclohexadienyl, 1,4-cyclohexadienyl, cycloheptyl, 1,3-cycloheptadienyl, 1,3,5-cycloheptatrienyl, cyclooctyl, cyclooctadienyl, indanyl and the like. Cycloalkyl may be optionally substituted where allowed by available valences. In certain embodiments, cycloalkyl is selected from C3-C20cycloalkyl, C3-C14cycloalkyl, C5-C8cycloalkyl, C3-C8cycloalkyl and the like.
As used herein, the term “alkenyl” generally refers to linear or branched alkyl radicals having one or more carbon-carbon double bonds, such as C2 to C8 and C2 to C6 alkenyl, including 3-propenyl and the like, and may be optionally substituted where allowed by available valences.
As used herein, the term “alkynyl” generally refers to linear or branched alkyl radicals having one or more carbon-carbon triple bonds, such as C2 to C8 and C2 to C6 alkynyl, including hex-3-yne and the like and may be optionally substituted where allowed by available valences.
As used herein, the term “aryl” refers to a monocarbocyclic, bicarbocyclic or polycarbocyclic aromatic ring structure. Included in the scope of aryl are aromatic rings having from six to twenty carbon atoms. Aryl ring structures include compounds having one or more ring structures, such as mono-, bi-, or tricyclic compounds. Examples of aryl include phenyl, tolyl, anthracenyl, fluorenyl, indenyl, azulenyl, phenanthrenyl (i.e., phenanthrene), napthyl (i.e., napthalene) and the like. In certain embodiments, aryl may be optionally substituted where allowed by available valences. In one embodiment, aryl is an optionally substituted phenyl or naphthyl.
As used herein, the term “heteroaryl” refers to monocyclic, bicyclic or polycyclic aromatic ring structures in which one or more atoms in the ring, is an element other than carbon (heteroatom). Heteroatoms are typically O, S or N atoms. Included within the scope of heteroaryl, and independently selectable, are O, N, and S heteroaryl ring structures. The ring structure may include compounds having one or more ring structures, such as mono-, bi-, or tricyclic compounds. In some embodiments, heteroaryl may be selected from ring structures that contain one or more heteroatoms, two or more heteroatoms, three or more heteroatoms, or four or more heteroatoms. In one embodiment, the heteroaryl is a 5 to 10 membered or 5 to 12 membered heteroaryl. Heteroaryl ring structures may be selected from those that contain five or more atoms, six or more atoms, or eight or more atoms. Examples of heteroaryl ring structures include, but are not limited to: acridinyl, benzimidazolyl, benzoxazolyl, benzofuranyl, benzothiazolyl, benzothienyl, 1,3-diazinyl, 1,2-diazinyl, 1,2-diazolyl, 1,4-diazanaphthalenyl, furanyl, furazanyl, imidazolyl, indazolyl, indolyl, isoxazolyl, isoquinolinyl, isothiazolyl, isoindolyl, oxadiazolyl, oxazolyl, purinyl, pyridazinyl, pyrazolyl, pyridinyl, pyrazinyl, pyrimidinyl, pyrrolyl, quinazolinyl, quinolinyl, quinoxalinyl, thiazole-2(3H) imine, 1,3,4,-thiadiazole-2(3H)-imine-yl, thiazolyl, thiophenyl, 1,3,5-triazinyl, 1,2,4-triazinyl, 1,2,3-triazinyl, tetrazolyl and the like. In certain embodiments, heteroaryl may be optionally substituted where allowed by available valences.
As used herein, the term “alkoxy” generally refers to a structure of the formula: —O—R. In certain embodiments, R may be an optionally substituted straight or branched alkyl, such as a C1 to C5 alkyl.
As used herein, the term “alkylthio” generally refers to a structure of the formula: —S—R. In certain embodiments, R may be an optionally substituted straight or branched alkyl, such as a C1 to C5 alkyl.
As used herein, the term “amino” generally refers to a structure of the formula: —NRR′. In certain embodiments, R and R′ independently may be H or an optionally substituted straight or branched alkyl, such as a C1 to C5 alkyl. In one embodiment, “thiazoleamino” refers to an amino, wherein at least one of R or R′ is a 2-thiazolyl, 3-thiazolyl or 4-thiazolyl. In one embodiment, “alkylamino” refers to an amino, wherein at least one of R or R′ is an optionally substituted straight or branched C1 to C5 alkyl.
As used herein, the term “acetamino” generally refers to a structure of the formula: —NR(C(═O)CH3), wherein R may be H or an optionally substituted straight or branched alkyl, such as a C1 to C5 alkyl.
As used herein, the term “acetamide” generally refers to a structure of the formula: C(═O)NH2.
As used herein, the term “sulfonyl” generally refers to a structure of the formula: —SO2R, wherein R can be H or an optional substituent including, but not limited to straight or branched C1 to C6 alkyl, aryl, heteroaryl, cycloalkyl, or heterocycle. In one embodiment, “alkylsulfonyl” refers to a structure of the formula: —SO2R, wherein R is an optionally substituted straight or branched C1 to C6 alkyl.
As used herein, the term “oxo” generally refers to a structure of the formula: (═O).
As used herein, the term “phenyloxy” generally refers to a structure of the formula: —O-phenyl, wherein phenyl can be optionally substituted.
For the purposes of this disclosure, the terms “halogen” or “halo” refer to substituents independently selected from fluorine, chlorine, bromine, and iodine.
As used herein, the terms “Compound” or “Compound provided herein” generally refer to a compound described in Section 5.1 or Example 6. In one embodiment, the terms refer to a compound of Formula I, II, III or IV. In another embodiment, the terms refer to a compound of Formula Ia, IIa, IIIa or IVa. In a specific embodiment, the terms refer to a compound depicted in Table 1. In one embodiment, the terms refer to a Compound disclosed in WO2005/089764, e.g., Compounds in the table on pages 26-98; WO2006/113703, e.g., Compounds in the table on pages 29-102; WO2008/127715, e.g., Compounds in the table on pages 52-126; WO2008/127714, e.g., Compounds in the table on pages 48-123; and U.S. Provisional Patent Application Ser. No. 61/181,653 entitled: METHODS FOR TREATING CANCER AND NON-NEOPLASTIC CONDITIONS, filed May 27, 2009, all of which are herewith incorporated by reference in their entirety. In one embodiment, the terms refer to a particular enantiomer, such as an R or S enantiomer of a “Compound” or “Compound provided herein”. In one embodiment, the terms refer to an R or S enantiomer of a compound of Formula I, II, III or IV. In another embodiment, the terms refer to an R or S enantiomer of a compound of Formula Ia, IIa, IIIa or IVa. In a specific embodiment, the terms refer to an R or S enantiomer of a compound depicted in Table 1. The “Compound” or “Compound provided herein” may comprise one or more asymmetric carbon atoms, i.e. n asymmetric carbon atoms, having either R or S configuration as determined by a person skilled in the art. It is understood that the terms “Compound” or “Compound provided herein” encompass all possible stereoisomers that may be generated based on all asymmetric carbon atoms. For example, if a Compound has two (n=2) assymetric carbon atoms, the terms “Compound” or “Compound provided herein” encompass all four, i.e. 2n=22=4, stereoisomers (R,S; R,R; S,S; S;R). The “Compound” or “Compound provided herein” may be a substantially pure (e.g., about 90%, about 95%, about 98%, about 99%, or about 99.9% pure) single stereoisomer or a mixture of two or more stereoisomers.
As used herein, the terms “self-microemulsifying drug delivery system” (SMEDDS) or “self-emulsifying drug delivery system” (SEDDS) mean a composition that contains an active agent herein defined in intimate admixture with pharmaceutically acceptable excipients such that the system is capable of dissolving the active agent to the desired concentration and producing colloidal structures by spontaneously forming a microemulsion when diluted with an aqueous medium, for example water, or in gastric juices. The colloidal structures can be solid or liquid particles including droplets and nanoparticles. In a SEDDS or SMEDDS system the type of microemulsion produced will be either clear or turbid depending on drug loading and the type of surfactant used.
As used herein, “microemulsion” means a slightly opaque, opalescent, non-opaque or substantially non-opaque colloidal dispersion (i.e. “clear”) that is formed spontaneously or substantially spontaneously when its components are brought into contact with an aqueous medium. A microemulsion is thermodynamically stable and typically contains dispersed droplets of a mean diameter less than about 200 nm (2000 Å). Generally microemulsions comprise droplets or liquid nanoparticles that have a mean diameter of less than about 150 nm (1500 Å); typically less than 100 nm, generally greater than 10 nm, wherein the dispersion may be thermodynamically stable over a time period of up to about 24 hours.
As used herein, the terms “pathologic,” “pathological” or “pathologically-induced,” in the context of the production of VEGF described herein, refer to the stress-induced expression of VEGF protein. In one embodiment, oncongenic transformation-induced expression of VEGF protein by tumor cells or other cells in the tumor environment is encompassed by the terms. In another embodiment, hypoxia-induced expression of VEGF protein in a chronic or traumatic inflammatory condition is encompassed by the terms. In another embodiment, in response to environmental stimuli, cells that disregulate or overproduce VEGF protein is also encompassed by the terms. As applicable, expression of VEGF protein supports inflammation, angiogenesis and tumor growth. The inhibition or reduction in pathological production of VEGF protein by a Compound can be assessed in cell culture and/or animal models as described herein.
As used herein, the term “about” means a range around a given value wherein the resulting value is substantially the same as the expressly recited value. In one embodiment, “about” means within 25% of a given value or range. For example, the phrase “about 70% by weight” comprises at least all values from 52% to 88% by weight. In another embodiment, the term “about” means within 10% of a given value or range. For example, the phrase “about 70% by weight” comprises at least all values from 63% to 77% by weight. In another embodiment, the term “about” means within 7% of a given value or range. For example, the phrase “about 70% by weight” comprises at least all values from 65% to 75% by weight.
Presented herein are methods for treating breast cancer. In one aspect, the methods for treating breast cancer involve the administration of a Compound, as a single agent therapy, to a patient in need thereof. In a specific embodiment, presented herein is a method for treating breast cancer, comprising administering to a patient in need thereof an effective amount of a Compound, as a single agent. In another embodiment, presented herein is a method for treating breast cancer, comprising administering to a patient in need thereof a pharmaceutical composition comprising a Compound, as the single active ingredient, and a pharmaceutically acceptable carrier, excipient or vehicle.
In another aspect, the methods for treating breast cancer involve the administration of a Compound in combination with another therapy (e.g., one or more additional therapies that do not comprise a Compound, or that comprise a different Compound) to a patient in need thereof. Such methods may involve administering a Compound prior to, concurrent with, or subsequent to administration of the additional therapy. In certain embodiments, such methods have an additive or synergistic effect. In a specific embodiment, presented herein is a method for treating breast cancer, comprising administering to a patient in need thereof an effective amount of a Compound and an effective amount of another therapy.
In certain embodiments, the concentration of VEGF or other angiogenic or inflammatory mediators in biological specimens (e.g., plasma, serum, cerebral spinal fluid, urine or any other biofluids) of a patient is monitored before, during and/or after a course of treatment involving the administration of a Compound or a pharmaceutical composition thereof to the patient. In certain embodiments, the tumoral blood flow or metabolism, or peritumoral inflammation or edema in a patient is monitored before, during and/or after a course of treatment involving the administration of a Compound or a pharmaceutical composition thereof to the patient. The dosage, frequency and/or length of administration of a Compound or a pharmaceutical composition thereof to a patient may also be modified as a result of the concentration of VEGF or other angiogenic or inflammatory mediators, or tumoral blood flow or metabolism, or peritumoral inflammation or edema. Alternatively, changes in one or more of these parameters (e.g., the concentration of VEGF or other angiogenic or inflammatory mediators, or tumoral blood flow or metabolism, or peritumoral inflammation or edema) might indicate that the course of treatment involving the administration of the Compound or pharmaceutical composition thereof is effective in treating breast cancer.
In a specific embodiment, presented herein is a method for treating breast cancer, comprising: (a) administering to a patient in need thereof one or more doses of a Compound or a pharmaceutical composition thereof; and (b) monitoring the concentration of VEGF or other angiogenic or inflammatory mediators (e.g., detected in biological specimens such as plasma, serum, cerebral spinal fluid, urine or other biofluids), and/or or monitoring tumoral blood flow or metabolism, or peritumoral inflammation or edema before and/or after step (a). In certain embodiments, step (b) comprises monitoring the concentration of one or more inflammatory mediators including, but not limited to, cytokines and interleukins such as IL-6 and IL-8. In particular embodiments, step (b) comprises monitoring the concentration of VEGF-R, P1GF, VEGF-C, and/or VEGF-D. In certain embodiments, the monitoring step (b) is carried out before and/or after a certain number of doses (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, or 20 doses, or more doses; or 2 to 4, 2 to 8, 2 to 20 or 2 to 30 doses) or a certain time period (e.g., 1, 2, 3, 4, 5, 6, or 7 days; or 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12, 15, 20, 30, 40, 45, 48 or 50 weeks), of administering the Compound. In certain embodiments, one or more of these monitoring parameters are detected prior to administration of the Compound or pharmaceutical composition thereof. In specific embodiments, a decrease in the concentration of VEGF or other angiogenic or inflammatory mediators, or a change in tumoral blood or metabolism, or peritumoral inflammation or edema following administration of the Compound or pharmaceutical composition thereof indicates that the course of treatment is effective for treating breast cancer. In some embodiments, a change in the concentration of VEGF or other angiogenic or inflammatory mediators, or a change in tumoral blood or metabolism, or peritumoral inflammation or edema following administration of the Compound or pharmaceutical composition thereof may indicate that the dosage, frequency and/or length of administration of the Compound or a pharmaceutical composition thereof may be adjusted (e.g., increased or reduced) or maintained.
The concentration of VEGF or other angiogenic or inflammatory mediators, or a change in tumoral blood or metabolism, or peritumoral inflammation or edema of a patient may be detected by any technique known to one of skill in the art. In certain embodiments, the method for detecting the concentration of VEGF or other angiogenic or inflammatory mediators in a patient involves obtaining a biological sample (e.g., a plasma sample, a serum sample, a cerebral spinal fluid sample, a urine sample, or other biofluid sample, or a tissue sample) from the patient and detecting the concentration of VEGF or the other angiogenic or inflammatory mediators in the biological sample or a sample therefrom that has been subjected to certain types of treatment (e.g., centrifugation) and detecting the concentration of VEGF or the other angiogenic or inflammatory mediators using immunological techniques, such as ELISA. In a specific embodiment, an ELISA described herein, e.g., in the working examples in Section 9 et seq., may be used to detect the concentration of VEGF or other angiogenic or inflammatory mediators in a biological sample or a sample therefrom that has been subjected to certain types of treatment (e.g., centrifugation). Other techniques known in the art that may be used to detect the concentration of VEGF or other angiogenic or inflammatory mediators in a biological sample or a sample therefrom that has been subjected to certain types of treatment include multiplex or proteomic assays. In a specific embodiment, an MRI, DCE-MRI, X-rays (e.g., a mammogram), ultrasound, CT scan, PET scan (e.g., positron emission mammography) or ductography may be used to detect the tumor blood flow or metabolism, or peritumoral inflammation or edema or inflammation.
In specific embodiments, the methods for treating breast cancer provided herein alleviate or manage one, two or more symptoms associated with breast cancer. Alleviating or managing one, two or more symptoms of breast cancer may be used as a clinical endpoint for efficacy of a Compound for treating breast cancer. In some embodiments, the methods for treating breast cancer provided herein reduce the duration and/or severity of one or more symptoms associated with breast cancer. In some embodiments, the methods for treating breast cancer provided herein inhibit the onset, progression and/or recurrence of one or more symptoms associated with breast cancer. In some embodiments, the methods for treating breast cancer provided herein reduce the number of symptoms associated with breast cancer.
Symptoms associated with breast cancer include, but are not limited to, a swelling or lump (mass) in the breast, swelling in the armpits (lymph nodes), nipple discharge (clear or bloody), pain in the breast nipple, an inverted or retracted nipple, scaly or pitted skin on the nipple, microcalcifications in tight clusters, and a dense mass with spiky outline. In addition to these symptoms, symptoms of metastatic breast cancer may also include bone pain, shortness of breath, a decrease in appetite, unintentional weight loss, headaches, neurological pain, and/or neurological weakness.
The methods for treating breast cancer provided herein inhibit or reduce pathological production of human VEGF. In particular embodiments, the methods for treating breast cancer provided herein selectively inhibit pathologic production of human VEGF (e.g., by the tumor), but do not disturb the physiological activity of human VEGF protein. Preferably, the methods for treating breast cancer provided herein do not significantly inhibit or reduce physiological or homeostatic production of human VEGF. For example, blood pressure, protein levels in urine, and bleeding are maintained within normal ranges in treated subjects. In a specific embodiment, the treatment does not result in adverse events as defined in Cancer Therapy Evaluation Program, Common Terminology Criteria for Adverse Events, Version 3.0, DCTD, NCI, NIH, DHHS Mar. 31, 2003 (cstep.cancer.gov), publish date Aug. 9, 2006, which is incorporated by reference herein in its entirety. In other embodiments, the methods for treating breast cancer provided herein do not result in adverse events of grade 2 or greater as defined in the Cancer Therapy Evaluation Program, Common Terminology Criteria for Adverse Events, Version 3.0, supra.
In specific embodiments, the methods for treating breast cancer provided herein inhibit or reduce pathological angiogenesis and/or tumor growth. In certain embodiments, the methods for treating breast cancer provided herein prolong or delay the G1/S or late G1/S phase of cell cycle (i.e., the period between the late resting or pre-DNA synthesis phase, and the early DNA synthesis phase).
In particular embodiments, the methods for treating breast cancer provided herein inhibit, reduce, diminish, arrest, or stabilize a tumor associated with breast cancer or a symptom thereof. In certain embodiments, the methods for treating breast cancer provided herein inhibit, reduce, diminish, arrest, or stabilize the blood flow, metabolism, peritumoral inflammation or peritumoral edema in a tumor associated with breast cancer or a symptom thereof. In some embodiments, the methods for treating breast cancer provided herein reduce, ameliorate, or alleviate the severity of breast cancer and/or a symptom thereof. In particular embodiments, the methods for treating breast cancer provided herein cause the regression of a tumor, tumor blood flow, tumor metabolism, or peritumoral inflammation or edema and/or a symptom associated with breast cancer. In other embodiments, the methods for treating breast cancer provided herein reduce hospitalization (e.g., the frequency or duration of hospitalization) of a subject diagnosed with breast cancer. In some embodiments, the methods for treating breast cancer provided herein reduce hospitalization length of a subject diagnosed with breast cancer. In certain embodiments, the methods provided herein increase the survival of a subject diagnosed with breast cancer. In particular embodiments, the methods for treating breast cancer provided herein inhibit or reduce the progression of one or more tumors or a symptom associated therewith.
In specific embodiments, the methods for treating breast cancer provided herein enhance or improve the therapeutic effect of another therapy (e.g., an anti-cancer agent, radiation, drug therapy such as chemotherapy, or surgery). In certain embodiments, the methods for treating breast cancer provided herein involve the use of a Compound as an adjuvant therapy. In certain embodiments, the methods for treating breast cancer provided herein improve the ease in removal of tumors (e.g., enhance resectability of the tumors) by reducing vascularization prior to surgery. In particular embodiments, the methods for treating breast cancer provided herein reduce vascularization after surgery, for example, reduce vascularization of the remaining tumor mass not removed by surgery. In some embodiments, the methods for treating breast cancer provided herein prevent recurrence, e.g., recurrence of vascularization and/or tumor growth.
In some embodiments, the methods for treating breast cancer provided herein reduce the growth of a tumor or neoplasm associated with breast cancer. In other embodiments, the methods for treating breast cancer provided herein decrease tumor size of breast cancer-associated tumors. In certain embodiments, the methods for treating breast cancer provided herein reduce the formation of a tumor such as a breast cancer-associated tumor. In certain embodiments, the methods for treating breast cancer provided herein eradicate, remove, or control primary, regional and/or metastatic tumors associated with breast cancer. In other embodiments, the methods for treating breast cancer provided herein decrease the number or size of metastases associated with breast cancer. In particular embodiments, the methods for treating breast cancer provided herein the reduce the mortality of subjects diagnosed with breast cancer. In other embodiments, the methods for treating breast cancer provided herein increase the cancer-free survival rate of patients diagnosed with breast cancer. In some embodiments, the methods for treating breast cancer provided herein increase relapse-free survival. In certain embodiments, the methods for treating breast cancer provided herein increase the number of patients in remission or decrease the hospitalization rate. In other embodiments, the methods for treating breast cancer provided herein maintain the size of the tumor so that it does not increase, or so that it increases by less than the increase of a tumor after administration of a standard therapy as measured by conventional methods available to one of skill in the art, such as X-ray (e.g., mammogram), ultrasound, CT scan, MRI, DCE-MRI and PET scan (e.g., positron emission mammography). In other embodiments, the methods for treating breast cancer provided herein prevent the development or onset of one or more symptoms associated with breast cancer. In other embodiments, the methods for treating breast cancer provided herein increase the length of remission in patients. In particular embodiments, the methods for treating breast cancer provided herein increase symptom-free survival of breast cancer patients. In some embodiments, the methods for treating breast cancer provided herein do not cure breast cancer in patients, but prevent the progression or worsening of the disease. In specific embodiments, the methods for treating breast cancer achieve one or more of the clinical endpoints set forth in the working examples in Section 11 et seq. In particular embodiments, the methods for treating breast cancer provided herein achieve one or more of the following: (i) inhibition or reduction in pathological production of VEGF; (ii) stabilization or reduction of peritumoral inflammation or edema in a subject; (iii) reduction in the concentration of VEGF or other angiogenic or inflammatory mediators (e.g., cytokines or interleukins) in biological specimens (e.g., plasma, serum, cerebral spinal fluid, urine or other biofluids); (iv) inhibition or decrease in tumor metabolism or perfusion; (v) inhibition or decrease in angiogenesis or vascularization; and (vi) an improvement in quality of life as assessed by methods well know in the art. In specific embodiments, the methods for treating breast cancer provided herein reduce the concentration of one, two or more, or all of the following in biological specimens (e.g., plasma, serum, cerebral spinal fluid, urine or other biofluids): P1GF, VEGF-C, VEGF-D, VEGF-R, IL-6 and/or IL-8.
In certain aspects, the methods for treating breast cancer provided herein reduce the tumor volume or tumor size (e.g., diameter) in a subject as determined by methods well known in the art, e.g., MRI, ultrasound, X-ray (e.g., mammogram), CT scan, or PET scan (e.g., positron emission mammography). Three dimensional volumetric measurement performed by MRI has been shown to be sensitive and consistent in assessing tumor size (see, e.g., Harris et al., Neurosurgery, June 2008, 62(6): 1314-9), and thus may be employed to assess tumor shrinkage in the methods provided herein. In specific embodiments, the methods for treating breast cancer provided herein reduce the tumor volume or tumor size (e.g., volume or diameter) in a subject by at least about 20% as assessed by methods well known in the art, e.g., MRI. In certain embodiments, the methods for treating breast cancer provided herein reduce the tumor volume or tumor size (e.g., volume or diameter) in a subject by at least about 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 80%, 85%, 90%, 95%, 98%, 99% or 100% relative to the tumor size prior to administration of a Compound, as assessed by methods well known in the art, e.g., MRI. In particular embodiments, the methods for treating breast cancer provided herein reduce the tumor volume or tumor size (e.g., volume or diameter) in a subject by at least an amount in a range of from about 10% to about 100% relative to the tumor size prior to administration of a Compound, as assessed by methods well known in the art, e.g., MRI. In particular embodiments, the methods provided herein reduce the tumor volume or tumor size (e.g., diameter) in a subject in an amount in a range of about 5% to 20%, 10% to 30%, 15% to 40%, 15% to 50%, 20% to 30%, 20% to 40%, 20% to 50%, 30% to 60%, 30% to 70%, 30% to 80%, 30% to 90%, 30% to 95%, 30% to 99%, 40% to 100%, or any percentage in between, relative to the tumor size prior to administration of a Compound, as assessed by methods well known in the art, e.g., MRI.
In particular aspects, the methods for treating breast cancer provided herein inhibit or decrease tumor perfusion in a subject as assessed by methods well known in the art, e.g., DCE-MRI. Standard protocols for DCE-MRI have been described (see, e.g., Morgan et al., J. Clin. Oncol., Nov. 1, 2003, 21(21):3955-64; Leach et al., Br. J. Cancer, May 9, 2005, 92(9):1599-610; Liu et al., J. Clin. Oncol., August 2005, 23(24): 5464-73; and Thomas et al., J. Clin. Oncol., Jun. 20, 2005, 23(18):4162-71) and can be applied in the methods provided herein. In specific embodiments, the methods for treating breast cancer provided herein inhibit or decrease tumor perfusion in a subject by at least about 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 80%, 85%, 90%, or 95% relative to tumor perfusion in the subject prior to administration of a Compound, as assessed by methods well known in the art, e.g., DCE-MRI. In particular embodiments, the methods for treating breast cancer provided herein inhibit or decrease tumor perfusion in a subject in an amount in the range of about 5% to 20%, 10% to 30%, 15% to 40%, 15% to 50%, 20% to 30%, 20% to 40%, 20% to 50%, 30% to 60%, 30% to 70%, 30% to 80%, 30% to 90%, 30% to 95%30% to 99%, 40% to 100%, or any percentage in between, relative to tumor perfusion in the subject prior to administration of a Compound, as assessed by methods well known in the art, e.g., DCE-MRI.
In particular aspects, the methods for treating breast cancer provided herein inhibit or decrease tumor metabolism in a subject as assessed by methods well known in the art, e.g., PET scanning such as fluorodeoxyglucose PET (FDG-PET) scanning Standard protocols for PET scanning (e.g., FDG-PET scanning) have been described and can be applied to the methods provided herein. In specific embodiments, the methods for treating breast cancer provided herein inhibit or decrease tumor metabolism in a subject by at least 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 80%, 85%, 90%, or 95% relative to tumor metabolism prior to administration of a Compound, as assessed by methods well known in the art, e.g., FDG-PET. In particular embodiments, the methods for treating breast cancer provided herein inhibit or decrease tumor metabolism in a subject in an amount in the range of about 5% to 20%, 10% to 30%, 10% to 100%, 15% to 40%, 15% to 50%, 20% to 30%, 20% to 40%, 20% to 50%, 30% to 60%, 30% to 70%, 30% to 80%, 30% to 90%, 30% to 95%30% to 99%, 40% to 100%, or any percentage in between, relative to tumor metabolism prior to administration of a Compound, as assessed by methods well known in the art, e.g., FDG-PET.
In specific aspects, the methods for treating breast cancer provided herein decrease the concentration of VEGF or other angiogenic or inflammatory mediators (e.g., cytokines or interleukins, such as IL-6) in a subject as assessed by methods well known in the art, e.g., ELISA. In specific embodiments, the methods for treating breast cancer provided herein decrease the concentration of VEGF or other angiogenic or inflammatory mediators (e.g., cytokines or interleukins, such as IL-6) in a subject by at least about 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 80%, 85%, 90%, 95%, or 100%, relative to the respective concentration prior to administration of a Compound, as assessed by methods well known in the art, e.g., ELISA. In particular embodiments, the methods for treating breast cancer provided herein decrease the concentration of VEGF or other angiogenic or inflammatory mediators (e.g., cytokines or interleukins, such as IL-6) in a subject by in the range of about 5% to 20%, 10% to 20%, 10% to 30%, 15% to 40%, 15% to 50%, 20% to 30%, 20% to 40%, 20% to 50%, 30% to 60%, 30% to 70%, 30% to 80%, 30% to 90%, 30% to 99%, 30% to 100%, or any percentage in between, relative to the respective concentration prior to administration of a Compound, as assessed by methods well known in the art, e.g., ELISA.
In specific aspects, the methods for treating breast cancer provided herein decrease the concentrations of P1GF, VEGF-C, VEGF-D, IL-6 and/or IL-8 in a subject as assessed by methods well known in the art, e.g., ELISA. In specific embodiments, the methods for treating breast cancer provided herein decrease the concentrations of P1GF, VEGF-C, VEGF-D, IL-6 and/or IL-8 in a subject by at least about 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 80%, 85%, 90%, 95%, or 100%, relative to the respective concentration prior to administration of a Compound, as assessed by methods well known in the art, e.g., ELISA. In particular embodiments, the methods for treating breast cancer provided herein decrease the concentrations of P1GF, VEGF-C, VEGF-D, IL-6 and/or IL-8 in a subject in the range of about 5% to 20%, 10% to 20%, 10% to 30%, 15% to 40%, 15% to 50%, 20% to 30%, 20% to 40%, 20% to 50%, 30% to 60%, 30% to 70%, 30% to 80%, 30% to 90%, 30% to 99%, 30% to 100%, or any percentage in between, relative to the respective concentration prior to administration of a Compound, as assessed by methods well known in the art, e.g., ELISA.
In specific embodiments, the methods for treating breast cancer provided herein inhibit or decrease pathological production of VEGF by at least about 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 80%, 85%, 90%, 95% or 100%, relative to the pathological production of VEGF observed prior to the administration of a Compound, as assessed by methods well known in the art, e.g., ELISA. In particular embodiments, the methods for treating breast cancer provided herein inhibit or decrease pathological production of VEGF in the range of about 5% to 10%, 10% to 20%, 10% to 30%, 15% to 40%, 15% to 50%, 20% to 30%, 20% to 40%, 20% to 50%, 30% to 60%, 30% to 70%, 30% to 80%, 30% to 90%, 30% to 99%, 30% to 100%, or any percentage in between, relative to the pathological production of VEGF observed prior to the administration of a Compound, as assessed by methods well known in the art, e.g., ELISA.
In specific embodiments, the methods for treating breast cancer provided herein inhibit or reduce angiogenesis or vascularization, by at least about 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 80%, 85%, 90%, 95%, or 100%, relative to angiogenesis or vascularization observed prior to administration of a Compound, as assessed by methods well known in the art, e.g., MRI, CT scan, or PET scan. In particular embodiments, the methods for treating breast cancer provided herein inhibit or reduce angiogenesis, in the range of about 5% to 10%, 10% to 20%, 10% to 30%, 15% to 40%, 15% to 50%, 20% to 30%, 20% to 40%, 20% to 50%, 30% to 60%, 30% to 70%, 30% to 80%, 30% to 90%, 30% to 99%, 30% to 100%, or any range in between, relative to angiogenesis or vascularization observed prior to administration of a Compound, as assessed by methods well known in the art, e.g., MRI, CT scan or PET scan.
In specific embodiments, the methods for treating breast cancer provided herein inhibit or reduce inflammation, by at least about 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 80%, 85%, 90%, 95%, or 100%, relative to inflammation observed prior to administration of a Compound, as assessed by methods well known in the art, e.g., MRI, CT scan, or PET scan. In particular embodiments, the methods for treating breast cancer provided herein inhibit or reduce inflammation, in the range of about 5% to 10%, 10% to 20%, 10% to 30%, 15% to 40%, 15% to 50%, 20% to 30%, 20% to 40%, 20% to 50%, 30% to 60%, 30% to 70%, 30% to 80%, 30% to 90%, 30% to 99%, 30% to 100%, or any percentage in between, relative to inflammation observed prior to administration of a Compound, as assessed by methods well known in the art, e.g., MRI, CT scan or PET scan.
In specific embodiments, the methods for treating breast cancer provided herein inhibit or reduce edema, by at least about 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 80%, 85%, 90%, 95%, or 100%, relative to edema observed prior to administration of a Compound, as assessed by methods well known in the art, e.g., MRI, CT scan, or PET scan. In particular embodiments, the methods for treating breast cancer provided herein inhibit or reduce edema, in the range of about 5% to 10%, 10% to 20%, 10% to 30%, 15% to 40%, 15% to 50%, 20% to 30%, 20% to 40%, 20% to 50%, 30% to 60%, 30% to 70%, 30% to 80%, 30% to 90%, 30% to 99%, 30% to 100%, or any percentage in between, relative to edema observed prior to administration of a Compound, as assessed by methods well known in the art, e.g., MRI, CT scan or PET scan.
In specific embodiments, the methods for treating breast cancer provided herein minimize the severity and/or frequency of one or more side effects observed with current anti-angiogenesis therapies. In certain embodiments, the methods for treating breast cancer provided herein do not cause one or more side effects observed with current anti-angiogenesis therapies. Such side effects include, but are not limited to, bleeding (usually transient, low-grade epistaxis), arterial and venous thrombosis (when given together with chemotherapy; probably secondary to thrombin-VEGF-VEGFR interactions, hypertension (potentially due to secondary inhibition of endothelial nitric oxide production), delayed wound healing, asymptomatic proteinuria (resulting from disruption of normal glomerular filtration), nasal septal perforation, reversible posterior leukoencephalopathy syndrome in association with hypertension, light-headedness, ataxia, headache, hoarseness, nausea, vomiting, diarrhea, rash, subungual hemorrhage, myelosuppression, fatigue, hypothyroidism, QT interval prolongation, and heart failure.
5.1 Compounds
In one embodiment, provided herein are Compounds having Formula (I):
or a pharmaceutically acceptable salt, racemate or stereoisomer thereof, wherein,
In one embodiment, the compound of Formula (I) is other than:
As will be evident to one of skill in the art, Compounds provided herein comprise at least one stereocenter, and may exist as a racemic mixture or as an enantiomerically pure composition. In one embodiment, a Compound provided herein is the (S) isomer, in an enantiomerically pure composition. In certain embodiments, the enantiomeric excess (e.e.) is about 90%, about 95%, about 99% or about 99.9% or greater.
In another embodiment, provided herein are Compounds having Formula (II):
or a pharmaceutically acceptable salt, racemate or stereoisomer thereof, wherein,
In another embodiment, provided herein are Compounds having Formula (II):
or a pharmaceutically acceptable salt, racemate or stereoisomer thereof, wherein,
In one embodiment, X is chloro or bromo.
In one embodiment, Rd is chloro or bromo.
In one embodiment, Ro is ORa.
In one embodiment, Ra is methyl, ethyl, propyl, isopropyl, butyl, or pentyl, each optionally substituted with one or more hydroxyl substituents.
In another embodiment, provided herein are Compounds having Formula (II):
or a pharmaceutically acceptable salt, racemate or stereoisomer thereof, wherein,
In another embodiment, provided herein are Compounds having Formula (III):
or a pharmaceutically acceptable salt, racemate or stereoisomer thereof, wherein,
In another embodiment, provided herein are Compounds having Formula (IV):
or a pharmaceutically acceptable salt, racemate or stereoisomer thereof, wherein,
In another embodiment, provided herein are Compounds having Formula (IV):
or a pharmaceutically acceptable salt, racemate or stereoisomer thereof, wherein,
In another embodiment, the Compounds set forth above having a formula selected from Formula (Ia), Formula (IIa), Formula (IIIa) and Formula (IVa):
Illustrative examples of Compounds or a pharmaceutically acceptable salt, racemate or stereoisomer thereof provided herein include:
In a further embodiment, additional examples of the Compounds provided herein are disclosed in International Patent Application Publication No. WO2005/089764 (“'764 publication”) on pages 26 to 98, and in copending U.S. Provisional Patent Application 61/181,653, entitled: METHODS FOR TREATING CANCER AND NON-NEOPLASTIC CONDITIONS, filed May 27, 2009, each of which are incorporated by reference herein in their entirety. Methods for preparing certain Compounds provided herein and the Compounds disclosed on pages 26 to 98 of the '764 publication are provided on pages 99 to 105 and 112 to 142 of the '764 publication and are incorporated by reference herein in their entirety and for all purposes. Methods for preparing certain Compounds provided herein and the Compounds disclosed in copending U.S. Provisional Patent Application 61/181,652, entitled: PROCESSES FOR THE PREPARATION OF SUBSTITUTED TETRAHYDRO BETA-CARBOLINES, filed May 27, 2009, are provided therein and are incorporated by reference herein in their entirety and for all purposes.
5.2 Pharmaceutical Properties and Formulations
5.2.1 Activity
Without being bound by any theory, Compounds described herein inhibit the translation of pathologically expressed human VEGF mRNA and, thus, inhibit the pathologic production of human VEGF protein. In particular, the Compounds act specifically through a mechanism dependent on the 5′ untranslated region (UTR) of the human VEGF mRNA to inhibit the pathologic production of human VEGF protein. The activity of the Compounds tested is post-transcriptional since quantitative real-time polymerase chain reaction (PCR) assessments of mRNA have shown that the Compounds do not alter the levels of human VEGF mRNA. Analyses of the effects of the Compounds tested on ribosome association with VEGF transcripts indicate that the Compounds do not impede initiation of VEGF translation or promote dissociation of ribosomes from human VEGF mRNA.
Compounds are described that reduce or inhibit pathologic production of human VEGF (also known as VEGF-A and vascular permeability factor (VPF)). Exemplary Compounds have been shown to reduce or inhibit tumor production of VEGF as measured in cell culture and/or preclinical tumor models. Furthermore, the Compounds tested do not affect homeostatic, physiologically produced plasma VEGF levels in healthy humans.
By way of background, the human VEGF-A gene encodes a number of different products (isoforms) due to alternative splicing. The VEGF-A isoforms include VEGF121, VEGF165, VEGF189 and VEGF206 having 121, 165, 189 and 206 amino acids, respectively. VEGF165 and VEGF121 isoforms are soluble, whereas VEGF189 and VEGF206 isoforms are sequestered within the extracellular matrix. The activity of the Compounds tested was assessed by measuring the concentrations of soluble VEGF and/or extracellular matrix bound-VEGF in cell culture systems. In preclinical tumor models, the activity of the Compounds tested was assessed by measuring the concentrations of soluble VEGF. The data indicate that the Compounds tested inhibit the production of soluble as well as matrix associated forms of tumor derived VEGF.
In particular, a Compound provided herein has been shown to selectively inhibit stress (e.g., hypoxia) induced production of soluble human VEGF isoforms in cell culture without affecting soluble human VEGF production under normoxic conditions (see Sections 9.1.1.1 and 9.1.1.2). Thus, the Compound was shown to preferentially inhibit pathological production of soluble human VEGF isoforms resulting from hypoxia while sparing homeostatic production of soluble isoforms in unperturbed cells. Accordingly, in specific embodiments, a Compound selectively inhibits or reduces the pathological production of a soluble human VEGF isoform over inhibiting or reducing physiological production of a soluble human VEGF isoform.
A Compound provided herein has also shown to selectively inhibit pathological production of VEGF in tumor cells that constitutively overproduce VEGF even under normoxic conditions. See Section 9.1.1.3. In these studies, to better assess the Compound's activity, the inhibition of the pathological production of matrix-bound human VEGF was measured. Thus, in one embodiment, a Compound selectively inhibits or reduces the pathological production of a matrix-bound human VEGF isoform over inhibiting or reducing physiological production of a matrix-bound human VEGF isoform.
The ability of a Compound provided herein to inhibit pathologic production of human VEGF in cell culture has been demonstrated for multiple human tumor cells from a variety of different tissues. See Table 4 (Section 9.1.1.4).
Exemplary Compounds inhibited intratumoral and pathologic plasma human VEGF production in animal models with pre-established human tumors. See Sections 9.1.2.1 to 9.1.2.3. In addition to reducing pathological induced human VEGF concentrations and edema, inflammation, pathological angiogenesis and tumor growth, a Compound provided herein has been shown to selectively reduce intratumoral levels of human growth factors and cytokines, such as IL-6, IL-8, osteopontin, MCP-1 and VEGF family members including human VEGF-C, VEGF-D and placental growth factor (P1GF). See Sections 9.1.2.1. In particular, the Compound shows a dose-dependent reduction in the concentration of intratumoral and pathologic plasma soluble human VEGF isoforms (see Section 9.1.2.2, in particular
Compounds are described that reduce or inhibit edema, inflammation, pathological angiogenesis and tumor growth. A Compound provided herein has been shown to have a profound effect on the architecture of the tumor vasculature in animal models with pre-established human tumors. The Compound reduced the total volume and diameter of blood vessels formed compared to vehicle treated subjects. See Section 9.2.1. The Compound also showed inhibition of tumor growth in the same model. A dose-response effect of the Compound that correlated with decreases in tumor and pathologic plasma VEGF concentrations was observed when tumor size was assessed. See Section 9.2.2. Thus, in one embodiment, the concentration of soluble pathologically produced VEGF in human plasma may be used to assess and monitor the pharmacodynamic effect of a Compound provided herein. In a specific embodiment, the concentration of either VEGF121, VEGF165, or both in human plasma may be used to assess and monitor the pharmacodynamic effect of a Compound provided herein.
In concert with a decrease in pathological tumor induced production of VEGF, a Compound provided herein demonstrated tumor regression or delay of tumor growth in various xenograft models, including models of breast cancer, neuroblastoma, and prostate cancer. See Section 9.2.5. Compounds that inhibit tumor growth in multiple preclinical models are more likely to have clinical efficacy. See Johnson et al., Br. J. Cancer 2001, 84(10):1424-31. Further, a Compound provided herein has shown activity in an orthotopic SY5Y neuroblastoma and SKNEP ewing sarcoma tumor model. In orthotopic tumor models, human tumor cells are implanted into the mouse in an organ that corresponds to the location of the human cells from which a tumor would arise. Such models may provide a better predictor of clinical efficacy than injection of tumors into the flanks of nude mice. See Hoffman, Invest. New Drugs 1999, 17(4):343-59. See Section 9.2.5.6.
An in vivo study in rats administered a 14C-radiolabeled Compound provided herein has been shown that the Compound penetrates all tissues investigated after oral administration. See Section 9.2.6 and Table 23. In one embodiment, a Compound provided herein is able to penetrate cells, tissues or organs that are surrounded by an endothelial cell barrier. In a specific embodiment, a Compound penetrates endothelial cell barriers, such as, but not limited to, the blood-brain barrier, the blood-eye barrier, the blood-testes barrier, blood-uterus barrier, or the blood-ovary barrier. The cells, tissues or organs surrounded by an endothelial cell barrier are, for example, cerebellum, cerebrum, ovary, testis, or the eye. The ability of a Compound to traverse such endothelial barriers makes it suited for the treatment of cancers, such as brain cancers, including but not limited to glioblastoma or neurofibromatosis.
Provided herein are Compounds that provoke a delay or prolongation of the cell cycle.
In addition to its effects on pathological VEGF production, a Compound provided herein induces a late G1/early S-Phase cell cycle delay, i.e., between the late resting or pre-DNA synthesis phase, and the early in DNA synthesis phase in those tumor cell lines in which pathologic VEGF expression is decreased by the Compound. Further characterization indicates that this effect is concentration dependent, occurring at low nanomolar EC50 values similar to those associated with reducing pathological VEGF production. See Section 9.3.1.1. The effect seen is reversible upon cessation of exposure to a Compound. See Section 9.3.1.2. The cell cycle delay and inhibition of pathological VEGF protein production occur in concert, linking these phenotypes in inflammation, pathological angiogenesis and tumor growth. Inhibition of pathological VEGF production in the same tumor cells used herein with small interfering RNA (siRNA) does not induce a delay or prolongation of the cell cycle (data not shown). Conversely, the use of mimosine, a DNA synthesis inhibitor that halts cell cycle progression at the G1/S interface, does not delay or prolong the cell cycle or reduce VEGF production (data not shown). A Compound provided herein has demonstrated in an in vivo HT1080 xenograft model that the Compound delays cycling through the S-phase; an effect that is distinct from that of bevacizumab, which has no effect on tumor cell cycling. Thus, these experiments indicate that the effects of a Compound on the tumor cell cycle occur in parallel with its actions on pathological VEGF production in tumors.
5.2.2 Formulations
The Compounds provided herein can be administered to a patient orally or parenterally in the conventional form of preparations, such as capsules, microcapsules, tablets, granules, powder, troches, pills, suppositories, injections, suspensions and syrups. Suitable formulations can be prepared by methods commonly employed using conventional, organic or inorganic additives, such as an excipient selected from fillers or diluents, binders, disintegrants, lubricants, flavoring agents, preservatives, stabilizers, suspending agents, dispersing agents, surfactants, antioxidants or solubilizers.
Excipients that may be selected are known to those skilled in the art and include, but are not limited to fillers or diluents (e.g., sucrose, starch, mannitol, sorbitol, lactose, glucose, cellulose, talc, calcium phosphate or calcium carbonate and the like), a binder (e.g., cellulose, carboxymethylcellulose, methylcellulose, hydroxymethylcellulose, hydroxypropylmethylcellulose, polypropylpyrrolidone, polyvinylpyrrolidone, gelatin, gum arabic, polyethyleneglycol or starch and the like), a disintegrant (e.g., sodium starch glycolate, croscarmellose sodium and the like), a lubricant (e.g., magnesium stearate, light anhydrous silicic acid, talc or sodium lauryl sulfate and the like), a flavoring agent (e.g., citric acid, or menthol and the like), a preservative (e.g., sodium benzoate, sodium bisulfite, methylparaben or propylparaben and the like), a stabilizer (e.g., citric acid, sodium citrate or acetic acid and the like), a suspending agent (e.g., methylcellulose, polyvinyl pyrrolidone or aluminum stearate and the like), a dispersing agent (e.g., hydroxypropylmethylcellulose and the like), surfactants (e.g., sodium lauryl sulfate, polaxamer, polysorbates and the like), antioxidants (e.g., ethylene diamine tetraacetic acid (EDTA), butylated hydroxyl toluene (BHT) and the like) and solubilizers (e.g., polyethylene glycols, SOLUTOL®, GELUCIRE® and the like). The effective amount of the Compound provided herein in the pharmaceutical composition may be at a level that will exercise the desired effect. Effective amounts contemplated are further discussed in Section 5.4.
The dose of a Compound provided herein to be administered to a patient is rather widely variable and can be subject to the judgment of a health-care practitioner. In general, a Compound provided herein can be administered one to four times a day. The dosage may be properly varied depending on the age, body weight and medical condition of the patient and the type of administration. In one embodiment, one dose is given per day. In any given case, the amount of the Compound provided herein administered will depend on such factors as the solubility of the active component, the formulation used and the route of administration.
A Compound provided herein can be administered orally, with or without food or liquid.
The Compound provided herein can also be administered intradermally, intramuscularly, intraperitoneally, percutaneously, intravenously, subcutaneously, intranasally, epidurally, sublingually, intracerebrally, intravaginally, transdermally, rectally, mucosally, by inhalation, or topically to the ears, nose, eyes, or skin. The mode of administration is left to the discretion of the health-care practitioner, and can depend in-part upon the site of the medical condition.
In one embodiment, the Compound provided herein is administered orally using a capsule dosage form composition, wherein the capsule contains the Compound provided herein without an additional carrier, excipient or vehicle.
In another embodiment, provided herein are compositions comprising an effective amount of a Compound provided herein and a pharmaceutically acceptable carrier or vehicle, wherein a pharmaceutically acceptable carrier or vehicle can comprise one or more excipients, or a mixture thereof. In one embodiment, the composition is a pharmaceutical composition.
Compositions can be formulated to contain a daily dose, or a convenient fraction of a daily dose, in a dosage unit. In general, the composition is prepared according to known methods in pharmaceutical chemistry. Capsules can be prepared by mixing a Compound provided herein with one or more suitable carriers or excipients and filling the proper amount of the mixture in capsules.
One embodiment, provided herein is a SEDDS or SMEDDS system comprising a Compound provided herein (e.g., an effective amount of a composition provided herein), and a carrier medium comprising a lipophilic component, a surfactant, and optionally a hydrophilic component. In certain embodiments, the present disclosure provides a SEDDS or SMEDDS system comprising a Compound provided herein, and a carrier medium comprising one or more surfactants and optionally one or more additives.
In certain embodiments, the SEDDS or SMEDDS system is suitable for oral administration.
One embodiment, provided herein is a SEDDS or SMEDDS system comprising a representative Compound provided herein and a carrier medium that comprises a lipophilic component, a surfactant, optionally a hydrophilic component and optionally an additive.
In one embodiment, the SEDDS or SMEDDS system forms an o/w (oil-in-water) microemulsion when diluted with water.
In one embodiment, of a SEDDS or SMEDDS system provided herein is a microemulsion comprising a Compound provided herein. In certain embodiments, the microemulsion is an o/w (oil-in-water) microemulsion. In one embodiment, the microemulsion comprises a Compound provided herein, a lipophilic component, a surfactant, water, and optionally a hydrophilic component and optionally an additive. In one embodiment, the microemulsion comprises a Compound provided herein, a lipophilic component, a surfactant, and water. In one embodiment, the microemulsion comprises a Compound provided herein, a surfactant, water, and optionally an additive.
The colloidal structures of the microemulsion form spontaneously or substantially spontaneously when the components of the SEDDS or SMEDDS system are brought into contact with an aqueous medium, e.g., by simple shaking by hand for a short period of time, for example for about 10 seconds. The SEDDS or SMEDDS system provided herein is thermodynamically stable, e.g., for at least 15 minutes or up to 4 hours, even to 24 hours. Typically, the system contains dispersed structures, i.e., droplets or liquid nanoparticles of a mean diameter less than about 200 nm (2,000 Å), e.g., less than about 150 nm (1,500 Å), typically less than about 100 nm (1,000 Å), generally greater than about 10 nm (100 Å) as measured by standard light scattering techniques, e.g., using a MALVERN ZETASIZER 300TH particle characterizing machine. Solid drug particles of mean diameter greater than 200 nm may also be present. The proportion of particles present may be temperature dependent.
In accordance with the present disclosure, Compounds provided herein may be present in an amount of up to about 20% by weight of the SEDDS or SMEDDS system provided herein, e.g., from about 0.05% by weight. In one embodiment, the Compound provided herein is present in an amount of from about 0.05 to about 15% by weight of the composition, or in an amount of from about 0.1 to about 5% by weight of the SEDDS or SMEDDS system.
In some embodiments, the SEDDS or SMEDDS system provided herein further comprises a carrier medium having a lipophilic component and a surfactant. In other embodiments, the carrier medium also comprises a lipophilic component, a hydrophilic component and a surfactant. In further embodiments, the carrier medium may comprise a surfactant. In some embodiments, the carrier medium also comprises a surfactant and an additive. In certain embodiments, the Compound provided herein can reside in the lipophilic component or phase.
In some embodiments, the SEDDS or SMEDDS system, the carrier medium, and the microemulsion comprise one or more lipophilic substances. In certain embodiments, the SEDDS or SMEDDS system, the carrier medium, and the microemulsion comprise one or more hydrophilic substances. In other embodiments, the SEDDS or SMEDDS system, the carrier medium, and the microemulsion comprise one or more surfactants. In further embodiments, the SEDDS or SMEDDS system, the carrier medium, and the microemulsion comprise one or more additives.
The compositions provided herein can include a variety of additives including antioxidants, antimicrobial agents, enzyme inhibitors, stabilizers, preservatives, flavors, sweeteners and further components known to those skilled in the art.
A. Lipophilic Components
Lipophilic components include, but are not limited to:
A1) Medium Chain Fatty Acid Triglyceride
These include, but are not limited to, triglycerides of saturated fatty acid having 6 to 12, e.g. 8 to 10, carbon atoms. In one embodiment, the medium chain fatty acid triglycerides include, but are not limited to, those known and commercially available under the trade names ACOMED®, LABRAFAC®, MYRITOL®, CAPTEX®, NEOBEE®M 5 F, MIGLYOL® 810, MIGLYOL® 812, MIGLYOL® 818, MAZOL®, SEFSOL®860, SEFSOL® 870. In one embodiment, the lipophilic component is LABRAFAC®. In one embodiment, the lipophilic component is LABRAFAC®CC. In another embodiment, the lipophilic component is LABRAFAC® WL1349.
A2) Propylene Glycol Mono Fatty Acid Esters
The fatty acid constituent may include, but is not limited to, both saturated and unsaturated fatty acids having a chain length of from e.g. C8-C12. In one embodiment, the fatty acid is propylene glycol mono ester of caprylic and lauric acid as commercially available, e.g. under the trade names SEFSOL® 218, CAPRYOL®90 or LAUROGLYCOL®90, from e.g. Nikko Chemicals Co., Ltd. or Gattefossé or Capmul PG-8 from Abitec Corporation.
A3) Propylene Glycol Mono- and Di-Fatty Acid Esters
These include, but are not limited to, Laroglycol FCC and Capryol PGMC.
A4) Propylene Glycol Diesters
These include, but are not limited to, propylene glycol di-fatty acid esters such as propylene glycol dicaprylate (which is commercially available under the trade name MIGLYOL® 840 from e.g. sasol; Fiedler, H. P. “Lexikon der Hilfsstoffe für Pharmazie, Kosmetik and angrenzende Gebiete”, Edition Cantor, D-7960 Aulendorf, 4th revised and expanded edition (1996), volume 2, page 1008) or Captex 200 from Abitec Corporation.
A5) Propylene Glycol Monoacetate and Propylene Glycol
A6) Transesterified Ethoxylated Vegetable Oils
Transesterified ethoxylated vegetable oils are known and are commercially available under the trade name LABRAFIL® (H. Fiedler, loc. cit., vol 2, page 880). Examples are LABRAFIL® M 2125 CS (obtained from corn oil and having an acid value of less than about 2, a saponification value of 155 to 175, an HLB value of 3 to 4, and an iodine value of 90 to 110), and LABRAFIL® M 1944 CS (obtained from kernel oil and having an acid value of about 2, a saponification value of 145 to 175 and an iodine value of 60 to 90). LABRAFIL® M 2130 CS (which is a transesterification product of a C12-C18 glyceride and polyethylene glycol and which has a melting point of about 35 to about 40° C., an acid value of less than about 2, a saponification value of 185 to 200 and an iodine value of less than about 3) may also be used. LABRAFIL® lipophilic components can be obtained, for example, from Gattefossé (Paramus, N.J., USA).
In one embodiment, the alkylene polyol ethers or esters include products obtainable by transesterification of glycerides, e.g. triglycerides, with poly-(C2-C4 alkylene) glycols, e.g. poly-ethylene glycols and, optionally, glycerol. Such transesterification products are generally obtained by alcoholysis of glycerides, e.g. triglycerides, in the presence of a poly-(C2-C4 alkylene) glycol, e.g. polyethylene glycol and, optionally, glycerol (i.e. to effect transesterification from the glyceride to the poly-alkylene glycol/glycerol component, i.e. via poly-alkylene glycolysis/glycerolysis). In general such reaction is effected by reacting the indicated components (glyceride, polyalkylene glycol and, optionally, glycerol) at elevated temperature under an inert atmosphere with continuous agitation.
In one embodiment, the glycerides are fatty acid triglycerides, e.g. (C10-C22 fatty acid) triglycerides, including natural and hydrogenated oils, in particular vegetable oils. In one embodiment, vegetable oils include, for example, olive, almond, peanut, coconut, palm, soybean and wheat germ oils and, in particular, natural or hydrogenated oils rich in (C12-C18 fatty acid) ester residues. In one embodiment, polyalkylene glycol materials are polyethylene glycols, in particular polyethylene glycols having a molecular weight of from ca. 500 to ca. 4,000, e.g. from ca. 1,000 to ca. 2,000.
In one embodiment, alkylene polyol ethers or esters include, but are not limited to, mixtures of C3-C5 alkylene triol esters, e.g. mono-, di- and tri-esters in variable relative amount, and poly (C2-C4 alkylene) glycol mono- and di-esters, together with minor amounts of free C3-C5 alkylene triol and free poly-(C2-C5 alkylene) glycol. As hereinabove set forth, in one embodiment, the alkylene triol moiety is glyceryl; in another embodiment, the polyalkylene glycol moieties include, but are not limited to, polyethylene glycol, in certain embodiments, having a molecular weight of from ca. 500 to ca. 4,000; and in another embodiment, the fatty acid moieties will be C10-C22 fatty acid ester residues, in certain embodiments, saturated C10-C22 fatty acid ester residues.
In one embodiment, the alkylene polyol ethers or esters include transesterification products of a natural or hydrogenated vegetable oil and a polyethylene glycol and, optionally, glycerol; or compositions comprising or consisting of glyceryl mono-, di- and tri-C10-C22 fatty acid esters and polyethylene glycol mono- and di-C10-C22 fatty esters (optionally together with, e.g. minor amounts of free glycerol and free polyethylene glycol).
In one embodiment, the alkylene polyol ethers or esters include, but are not limited, those commercially available under the trade name GELUCIRE® from e.g. Gattefossé, in particular the products:
a) GELUCIRE® 33/01, which has an m.p.=ca. 33-37° C. and a saponification value of about 230-255;
b) GELUCIRE® 39/01, m.p.=ca. 37.5-41.5° C., saponification value of about 225-245; and
c) GELUCIRE® 43/01, m.p.=ca. 42-46° C., saponification value of about 220-240.
Products (a) to (c) above all have an acid value of maximum of 3. The SEDDS or SMEDDS system provided herein may include mixtures of such ethers or esters.
B. Surfactants
The SEDDS or SMEDDS system provided herein can contain one or more surfactants to reduce the emulsion's interfacial tension thereby providing thermodynamic stability. Surfactants may be complex mixtures containing side products or unreacted starting products involved in the preparation thereof, e.g. surfactants made by polyoxyethylation may contain another side product, e.g. polyethylene glycol.
In one embodiment, surfactants include, but are not limited to:
B1) Polyoxyethylene Mono Esters of a Saturated C10 to C22 Polymer
These include, but are not limited to, C11 substituted e.g. hydroxy fatty acid; e.g. 12 hydroxy stearic acid PEG ester, e.g. of PEG about e.g. 600-900, e.g. 660 Daltons MW, e.g. SOLUTOL® HS15 from BASF (Ludwigshafen, Germany). SOLUTOL® HS15, according to the BASF technical information (July 2003), comprises polyglycol mono- and di-esters of 12-hydroxystearic acid (=lipophilic part) and about 30% of free polyethylene glycol (=hydrophilic part). A small part of the 12-hydroxy group can be etherified with polyethylene glycol. SOLUTOL® HS15 has a hydrogenation value of 90 to 110, a saponification value of 53 to 63, an acid number of maximum 1, an iodine value of maximum 2, and a maximum water content of about 0.5% by weight. In one embodiment, the surfactant is SOLUTOL® HS15.
B2) Alkylene Polyol Ethers or Esters
In one embodiment, the alkylene polyol ethers or esters as described above for use in the pharmaceutical compositions provided herein include those commercially available under the trade name GELUCIRE® from e.g. Gattefossé(Paramus, N.J., USA), in particular the products:
a) GELUCIRE® 44/14, m.p.=ca. 42.5-47.5° C., saponification value of about 79-93;
b) GELUCIRE® 50/13, m.p.=ca. 46-51° C., saponification value of about 67-81;
Products (a) to (b) above both have an acid value of maximum of 2.
In one embodiment, the alkylene polyol ethers or esters have an iodine value of maximum 2. The SEDDS or SMEDDS system provided herein may further include mixtures of such ethers or esters.
GELUCIRE® products are inert semi-solid waxy materials with amphiphilic character. They are identified by their melting point and their HLB value. Most GELUCIRE® grades are saturated polyglycolised glycerides obtainable by polyglycolysis of natural hydrogenated vegetable oils with polyethylene glycols. They are composed of a mixture of mono-, di- and tri-glycerides and mono- and di-fatty acid esters of polyethylene glycol. In one embodiment, the C10 glyceride is GELUCIRE® 44/14 which has a nominal melting point of 44° C. and an HLB of 14. GELUCIRE® 44/14 exhibits the following additional characterizing data: acid value of max. 2, iodine value of max. 2, saponification value of 79-93, hydroxyl value of 36-56, peroxide value of max. 6, alkaline impurities max. 80, water content max. 0.50, free glycerol content max. 3, monoglycerides content 3.0-8.0. (H. Fiedler, loc. cit., vol 1, page 676; manufacturer information).
In one embodiment, the surfactant is present in a range of from about 5 to about 99.9% by weight, or in a range of from about 30% to about 99.9% of the SEDDS or SMEDDS system provided herein.
In one embodiment, the surfactant comprises about 30% to about 70%, or about 40% to about 60% by weight of the carrier medium of the SEDDS or SMEDDS system provided herein.
In one embodiment, the SEDDS or SMEDDS system provided herein include additives e.g. antioxidants, flavors, sweeteners and other components known to those skilled in the art.
In one embodiment, the antioxidants include ascorbyl palmitate, butylated hydroxy anisole (BHA), 2,6-di-tert-butyl-4-methyl phenol (BHT) and tocopherols. In a further embodiment, the antioxidant is BHT.
In one embodiment, these additives may comprise about 0.005% to about 5% or about 0.01% to about 0.1% by weight of the total weight of the SEDDS or SMEDDS system. Antioxidants, or stabilizers typically provide up to about 0.005 to about 1% by weight based on the total weight of the composition. Sweetening or flavoring agents typically provide up to about 2.5% or 5% by weight based on the total weight of the composition.
The aforementioned additives can also include components that act as surfactants to solidify a liquid micro-emulsion pre-concentrate. These include solid polyethylene glycols (PEGs) and GELUCIRE® products, in one embodiment, the GELUCIRE® products include those such as GELUCIRE® 44/14 or GELUCIRE® 50/13.
When the SEDDS or SMEDDS system provided herein is combined with water or an aqueous solvent medium to obtain an emulsion, for example a microemulsion, the emulsion or microemulsion may be administered orally, for example in the form of a drinkable solution. The drinkable solution may comprise water or any other palatable aqueous system, such as fruit juice, milk and the like. In one embodiment, the relative proportion of the lipophilic component(s), the surfactant(s) and the hydrophilic component(s) lie within the “Microemulsion” region on a standard three way plot graph. The compositions will therefore be capable, on addition to an aqueous medium, of providing microemulsions, for example having a mean particle size of <200 nm.
In one embodiment, the carrier medium comprises about 30 to 70% by weight of one or more lipophilic components, wherein the one or more lipophilic components are a medium chain fatty acid triglyceride (Al), or a transesterified ethoxylated vegetable oil (A6). In a further embodiment, the medium chain fatty acid triglyceride (Al) is LABRAFAC® (Gattefossé, Paramus, N.J., USA). In another embodiment, the transesterified ethoxylated vegetable oil (A6) is LABRAFIL® (Gattefossé, Paramus, N.J., USA).
In one embodiment, the carrier medium comprises about 30 to 70% by weight of one or more surfactants, wherein the one or more surfactants are a polyoxyethylene mono ester (C5), an alkylene polyol ether or ester (C10), or a transesterified, polyoxyethylated caprylic-capric acid glyceride (C13). In a further embodiment, the polyoxyethylene mono ester (C5) is SOLUTOL® HS15 (BASF, Ludwigshafen, Germany). In another embodiment, the alkylene polyol ether or ester (C10) is GELUCIRE®44/14 (Gattefossé, Paramus, N.J., USA). In yet another embodiment, the transesterified, polyoxyethylated caprylic-capric acid glyceride (C13) is LABRASOL® (Gattefossé, Paramus, N.J., USA).
In one embodiment, the carrier medium comprises about 70% by weight LABRASOL®, about 18.3% by weight LABRAFAC® and about 11.7% by weight LABRAFIL®.
In one embodiment, the carrier medium comprises a range of about 65.1% to about 74.9% by weight LABRASOL®, a range of about 17.0% to about 19.6% by weight LABRAFAC® and a range of about 10.9% to about 12.5% by weight LABRAFIL®.
In one embodiment, the carrier medium comprises about 35% by weight LABRASOL®, about 35% by weight LABRAFAC® and about 30% by weight SOLUTOL® HS15.
In one embodiment, the carrier medium comprises a range of about 33.6% to about 37.4% by weight LABRASOL®, a range of about 33.6% to about 37.4% by weight LABRAFAC® and a range of about 27.9% to about 32.1% by weight SOLUTOL® HS15.
In one embodiment, the carrier medium comprises about 35% by weight LABRAFIL®, about 35% by weight LABRAFAC®, and about 30% by weight SOLUTOL®HS15.
In one embodiment, the carrier medium comprises a range of about 33.6% to about 37.4% by weight LABRAFIL®, a range of about 33.6% to about 37.4% by weight LABRAFAC®, and a range of about 27.9% to about 32.1% by weight SOLUTOL® HS15.
In one embodiment, the carrier medium comprises about 35% by weight GELUCIRE®44/14, about 35% by weight LABRAFAC®, and about 30% by weight SOLUTOL®HS15.
In one embodiment, the carrier medium comprises a range of about 33.6% to about 37.4% by weight GELUCIRE® 44/14, a range of about 33.6% to about 37.4% by weight LABRAFAC®, and a range of about 27.9% to about 32.1% by weight SOLUTOL® HS15.
In one embodiment, provided herein is a SEDDS or SMEDDS system comprising a Compound provided herein, and a carrier medium comprising one or more surfactants. In one embodiment, the SEDDS or SMEDDS system additionally comprises an additive.
In one embodiment, the SEDDS or SMEDDS system comprises about 0.01% to about 5% by weight of a Compound provided herein.
In one embodiment, the dispersible pharmaceutical composition comprises about 95% to 99.09% by weight of one or more surfactants, wherein the one or more surfactants are selected from a group comprising an alkylene polyol ether or ester (C10), and a polyoxyethylene mono ester (C5). In a further embodiment, the alkylene polyol ether or ester (C10) is GELUCIRE®44/14 (Gattefossé, Paramus, N.J., USA). In yet another embodiment, the polyoxyethylene mono ester (C5) is SOLUTOL® HS15 (BASF, Ludwigshafen, Germany).
In one embodiment, the dispersible pharmaceutical composition comprises about 0.01% to about 0.1% by weight of an additive selected from a group comprising an antioxidant and a preservative. In a further embodiment, the additive is 2,6-di-tert-butyl-4-methylphenol (BHT).
In one embodiment, the SEDDS or SMEDDS system comprises about 0.28% by weight of a Compound provided herein, about 49.87% by weight of GELUCIRE®44/14, about 49.84% by weight of SOLUTOL® HS15 and about 0.01% by weight of BHT.
In one embodiment, the SEDDS or SMEDDS system comprises a range of about 0.26% to about 0.30% by weight of a Compound provided herein, a range of about 46.4% to about 53.4% by weight of GELUCIRE®44/14, a range of about 46.4% to about 53.3% by weight of SOLUTOL® HS15 and a range of about 0.009% to about 0.011% by weight of BHT.
In one embodiment, the SEDDS or SMEDDS system comprises about 1.43% by weight of a Compound provided herein, about 49.87% by weight of GELUCIRE®44/14, about 48.69% by weight of SOLUTOL® HS15 and about 0.01% by weight of BHT.
In one embodiment, the SEDDS or SMEDDS system comprises a range of about 1.33% to about 1.53% by weight of a Compound provided herein, a range of about 46.4% to about 53.4% by weight of GELUCIRE®44/14, a range of about 45.3% to about 52.1% by weight of SOLUTOL® HS15 and a range of about 0.009% to about 0.011% by weight of BHT.
In one embodiment, the SEDDS or SMEDDS system comprises about 2.67% by weight of a Compound provided herein, about 49.87% by weight of GELUCIRE®44/14, about 47.45% by weight of SOLUTOL®HS15 and about 0.01% by weight of BHT.
In one embodiment, the SEDDS or SMEDDS system comprises a range of about 2.48% to about 2.86% by weight of a Compound provided herein, a range of about 46.4% to about 53.4% by weight of GELUCIRE®44/14, a range of about 44.1% to about 50.8% by weight of SOLUTOL® HS15 and a range of about 0.009% to about 0.011% by weight of BHT.
In one embodiment, when the SEDDS or SMEDDS system provided herein is used to fill capsules for use in oral administration. The capsule may have a soft or hard capsule shell, for example, the capsule may be made of gelatine.
One group of SEDDS or SMEDDS systems provided herein may, on addition to water, provide aqueous microemulsions having an average particle size of about <200 nm (2,000 Å), about <150 nm (1,500 Å), or about <100 nm (1,000 Å).
In one embodiment, the SEDDS or SMEDDS systems provided herein exhibit advantageous properties when administered orally; for example in terms of consistency and high level of bioavailability obtained in standard bioavailability trials.
Pharmacokinetic parameters, for example, drug substance absorption and measured for example as blood levels, also can become more predictable and problems in administration with erratic absorption may be eliminated or reduced. Additionally pharmaceutical compositions provided herein are effective with biosurfactants or tenside materials, for example bile salts, being present in the gastro-intestinal tract. That is, pharmaceutical compositions provided herein are fully dispersible in aqueous systems comprising such natural tensides and thus capable of providing emulsion or microemulsion systems and/or particulate systems in situ which are stable. The function of pharmaceutical compositions provided herein upon oral administration remain substantially independent of and/or unimpaired by the relative presence or absence of bile salts at any particular time or for any given individual. Compositions provided herein may also reduce variability in inter- and intra-patient dose response.
In one embodiment, provided herein is a SEDDS or SMEDDS system comprising a Compound provided herein, and a carrier medium comprising one or more lipophilic components and one or more surfactants.
5.3 Patient Populations
In some embodiments, a subject treated for breast cancer in accordance with the methods provided herein is a human who has or is diagnosed with breast cancer. In other embodiments, a subject treated for breast cancer in accordance with the methods provided herein is a human predisposed or susceptible to breast cancer. In some embodiments, a subject treated for breast cancer in accordance with the methods provided herein is a human at risk of developing breast cancer. In specific embodiments, a subject treated for breast cancer in accordance with the methods provided herein is human that meets one, two or more, or all of the criteria for subjects in the working examples in Section 11 et seq.
In one embodiment, a subject treated for breast cancer in accordance with the methods provided herein is an elderly human. In another embodiment, a subject treated for breast cancer in accordance with the methods provided herein is a human adult. In a specific embodiment, a subject treated for breast cancer in accordance with the methods provided herein is a human that is 18 years old or is older than 18 years old. In certain embodiments, a subject treated for breast cancer in accordance with the methods provided herein is a human that is 12 to 20 years old, 15 to 20 years old, 20 to 25 years old, 25 to 30 years old, 30 to 35 years old, 35 to 40 years old, 40 to 45 years old, 45 to 50 years old, 50 to 55 years old, 55 to 60 years old, 60 to 65 years old, 65 to 70 years old, 70 to 75 years old, 75 to 80 years old, 80 to 85 years old, 85 to 90 years old, 90 to 95 years old or 95 to 100 years old. In certain embodiments, a subject treated in accordance with the methods provided herein is a human child.
In specific embodiments, a subject treated for breast cancer in accordance with the methods provided herein is a human female. In other embodiments, a subject treated for breast cancer in accordance with the methods provided herein is a human male. In certain embodiments, a subject treated for breast cancer in accordance with the methods provided herein is a female human that is not pregnant or is not breastfeeding. In other embodiments, a subject treated for breast cancer in accordance with the methods provided herein is a female human that is pregnant or will become pregnant, or is breastfeeding. In one embodiment, a subject treated for breast cancer in accordance with the methods provided herein is a post-menopausal human female. In another embodiment, a subject treated for breast cancer in accordance with the methods provided herein is a pre-menopausal human female.
In specific embodiments, a subject treated for breast cancer in accordance with the methods provided herein has one or more tumors growing on the breast tissue. In particular embodiments, one or more of the tumors are metastatic. In other embodiments, one or more of the tumor is benign.
In particular embodiments, a subject treated for breast cancer in accordance with the methods provided herein has one or more hormone-receptor-positive tumors. Such hormone-receptor-positive tumors may be estrogen-receptor-positive tumors or progesterone-receptor positive tumors. In a specific embodiment, a subject treated for breast cancer in accordance with the methods provided herein is a post-menopausal human female that has one or more hormone-receptor-positive tumors. In another specific embodiment, a subject treated for breast cancer in accordance with the methods provided herein is a pre-menopausal human female that has one or more hormone-receptor-positive tumors. In particular embodiments, a subject treated for breast cancer in accordance with the methods provided herein has one or more HER2-positive tumors.
In certain embodiments, a subject treated in accordance with the methods provided herein hasductual carcinoma in-situ (DCIS). In some embodiments, a subject treated in accordance with the methods provided herein has infiltrating ductal carcinoma (IDC). In some embodiments, a subject treated in accordance with the methods provided herein has medullary carcinoma. In some embodiments, a subject treated in accordance with the methods provided herein has infiltrating lobular carcinoma (ILC). In some embodiments, a subject treated in accordance with the methods provided herein has tubular carcinoma. In some embodiments, a subject treated in accordance with the methods provided herein has inflammatory breast cancer (IBC).
In certain embodiments, a subject treated for breast cancer in accordance with the methods provided herein has been diagnosed with Stage IIIB, Stage IIIC, or Stage IV breast cancer. In Stage IIIB breast cancer, one or more tumors has grown into the chest wall or skin, and one of the following applies: (1) one or more tumors has not spread to the lymph nodes; (2) one or more tumors has spread to 1 to 3 axillary lymph nodes and/or internal mammary lymph nodes; (3) one or more tumors has spread to 4 to 9 axillary lymph nodes, or it has enlarged the internal mammary lymph nodes. In Stage IIIC breast cancer, one of the following applies: (1) one or more tumors has spread to 10 or more axillary lymph nodes; (2) one or more tumors has spread to the lymph nodes under the clavicle (collar bone); (3) one or more tumors has spread to the lymph nodes above the clavicle; (4) the internal mammary lymph nodes are enlarged; (5) one or more tumors has spread to 4 or more axillary lymph nodes and to the internal mammary lymph nodes. In Stage IV breast cancer, one or more tumors have spread to distant organs (the most common sites are the bone, liver, brain, or lung), or to lymph nodes far from the breast.
In some embodiments, a subject treated for breast cancer in accordance with the methods provided herein inherited breast cancer. In other embodiments, a subject treated for breast cancer in accordance with the methods provided herein developed breast cancer spontaneously through gene mutation.
In particular embodiments, a subject treated for breast cancer in accordance with the methods provided herein is a human that is in an immunocompromised state or immunosuppressed state. In certain embodiments, a subject treated for breast cancer in accordance with the methods provided herein is a human receiving or recovering from immunosuppressive therapy. In certain embodiments, a subject treated for breast cancer in accordance with the methods provided herein is a human who is, will or has undergone surgery, drug therapy such as chemotherapy, and/or radiation therapy.
In some embodiments, a subject treated for breast cancer in accordance with the methods provided herein is suffering from a condition, e.g., a stroke or cardiovascular condition that may require VEGF therapy, wherein the administration of anti-angiogenic therapies other than a Compound may be contraindicated. For example, in certain embodiments, a subject treated for breast cancer in accordance with the methods provided herein has suffered from a stroke or is suffering from a cardiovascular condition. In some embodiments, a subject treated for breast cancer in accordance with the methods provided herein is experiencing circulatory problems. In certain embodiments, a subject treated for breast cancer in accordance with the methods provided herein is a human with diabetic polyneuropathy or diabetic neuropathy. In some embodiments, a subject treated for breast cancer in accordance with the methods provided herein is a human receiving VEGF protein or VEGF gene therapy. In other embodiments, a subject treated for breast cancer in accordance with the methods provided herein is not a human receiving VEGF protein or VEGF gene therapy.
In some embodiments, a subject treated for breast cancer in accordance with the methods provided herein is administered a Compound or a pharmaceutical composition thereof, or a combination therapy before any adverse effects or intolerance to therapies other than the Compound develops. In some embodiments, a subject treated for breast cancer in accordance with the methods provided herein is a refractory patient. In a certain embodiment, a refractory patient is a patient with a tumor that is refractory to a standard therapy (e.g., surgery, radiation, and/or drug therapy such as chemotherapy). In certain embodiments, a patient with cancer associated with breast cancer, is refractory to a therapy when the cancer has not significantly been eradicated and/or the symptoms have not been significantly alleviated. The determination of whether a patient is refractory can be made either in vivo or in vitro by any method known in the art for assaying the effectiveness of a treatment of breast cancer, using art-accepted meanings of “refractory” in such a context. In various embodiments, a patient with breast cancer is refractory when one or more tumors associated with breast cancer, has not decreased or has increased. In various embodiments, a patient with cancer associated with breast cancer is refractory when one or more tumors metastasize and/or spreads to another organ.
In some embodiments, a subject treated for breast cancer in accordance with the methods provided herein is in remission. In certain embodiments, a subject treated for breast cancer in accordance with the methods provided herein is experiencing recurrence of one or more tumors associated with breast cancer.
In some embodiments, a subject treated for breast cancer in accordance with the methods provided herein is a human that has proven refractory to therapies other than treatment with a Compound, but is no longer on these therapies. In certain embodiments, a subject treated for breast cancer in accordance with the methods provided herein is a human already receiving one or more conventional anti-cancer therapies, such as surgery, drug therapy such as chemotherapy, or radiation. Among these patients are refractory patients, patients who are too young for conventional therapies, and patients with recurring tumors despite treatment with existing therapies.
In some embodiments, a subject treated for breast cancer in accordance with the methods provided herein is a human susceptible to adverse reactions to conventional therapies. In some embodiments, a subject treated for breast cancer in accordance with the methods provided herein is a human that has not received a therapy, e.g., drug therapy such as chemotherapy, surgery, or radiation therapy, prior to the administration of a Compound or a pharmaceutical composition thereof. In other embodiments, a subject treated for breast cancer in accordance with the methods provided herein is a human that has received a therapy prior to administration of a Compound. In some embodiments, a subject treated for breast cancer in accordance with the methods provided herein is a human that has experienced adverse side effects to the prior therapy or the prior therapy was discontinued due to unacceptable levels of toxicity to the human.
In some embodiments, a subject treated for breast cancer in accordance with the methods provided herein has had no prior exposure to another anti-angiogenic therapy (e.g., an anti-VEGF monoclonal antibody, an anti-VEGFR monoclonal antibody, a tyrosine kinase inhibitor, or other angiogenesis pathway modualator). In particular embodiments, a subject treated for breast cancer in accordance with the methods provided herein does not have uncontrolled hypertension, major bleeding, HIV infection or recent acute cardiovascular event. In some embodiments, a subject treated for breast cancer in accordance with the methods provided herein is not, has not and/or will not receive a drug that is primarily metabolized by CYP2D6. In particular embodiments, a subject treated for breast cancer in accordance with the methods provided herein has not and will not received a drug that is primarily metabolized by CYP2D6 1, 2, 3 or 4 weeks before receiving a Compound or a pharmaceutical composition thereof and 1, 2, 3 or 4 weeks after receiving the Compound or pharmaceutical composition. Examples of such drugs include, without limitation, some antidepressants (e.g., tricyclic antidepressants and selective serotonin uptake inhibitors), some antipsychotics, some beta-adrenergic receptor blockers, and certain anti-arrhythmics.
In specific embodiments, a subject treated for breast cancer in accordance with the methods provided herein is not, has not and/or will not receive tamoxifen. In particular embodiments, a subject treated for breast cancer in accordance with the methods provided herein has not and will not receive tamoxifen 1, 2, 3 or 4 weeks before receiving a Compound or a pharmaceutical composition thereof and 1, 2, 3 or 4 weeks after receiving the Compound or pharmaceutical composition. In other embodiments, a subject treated for breast cancer in accordance with the methods provided herein has received tamoxifen, e.g., for 1, 2, 3 or 4 weeks before receiving a Compound or a pharmaceutical composition thereof
5.4 Dosage and Administration
In accordance with the methods for treating breast cancer provided herein, a Compound or a pharmaceutical composition thereof can be administered to a subject in need thereof by a variety of routes in amounts which result in a beneficial or therapeutic effect. A Compound or pharmaceutical composition thereof may be orally administered to a subject in need thereof in accordance with the methods for treating breast cancer provided herein. The oral administration of a Compound or a pharmaceutical composition thereof may facilitate subjects in need of such treatment complying with a regimen for taking the Compound or pharmaceutical composition. Thus, in a specific embodiment, a compound or pharmaceutical composition thereof is administered orally to a subject in thereof.
Other routes of administration include, but are not limited to, intravenous, intrathecal, intradermal, intramuscular, subcutaneous, intranasal, inhalation, transdermal, topical, transmucosal, intracranial, intratumoral, epidural and intra-synovial. In one embodiment, a Compound or a pharmaceutical composition thereof is administered systemically (e.g., parenterally) to a subject in need thereof. In another embodiment, a Compound or a pharmaceutical composition thereof is administered locally (e.g., intratumorally) to a subject in need thereof. In one embodiment, a Compound or a pharmaceutical composition thereof is administered intrathecally or via a route that permits the Compound to cross the blood-brain barrier (e.g., orally).
Evaluation has indicated that Compound #10 penetrates the blood-brain barrier. Table 40 provides brain tissue plasma concentration ratios determined by whole-body autoradiography at specified times after a single oral administration of 14C-Compound #10 to rats (50 mg/kg).
In accordance with the methods for treating breast cancer provided herein that involve administration of a Compound in combination with one or more additional therapies, the Compound and one or more additional therapies may be administered by the same route or a different routes of administration.
The dosage and frequency of administration of a Compound or a pharmaceutical composition thereof is administered to a subject in need thereof in accordance with the methods for treating breast cancer provided herein will be efficacious while minimizing any side effects. The exact dosage and frequency of administration of a Compound or a pharmaceutical composition thereof can be determined by a practitioner, in light of factors related to the subject that requires treatment. Factors which may be taken into account include the severity of the disease state, general health of the subject, age, weight, and gender of the subject, diet, time and frequency of administration, drug combination(s), reaction sensitivities, and tolerance/response to therapy. The dosage and frequency of administration of a Compound or a pharmaceutical composition thereof may be adjusted over time to provide sufficient levels of the Compound or to maintain the desired effect.
In certain embodiments, a Compound or a pharmaceutical composition thereof is administered to a subject in need thereof in accordance with the methods for treating breast cancer provided herein at a dosage and a frequency of administration that achieves one or more of the following: (i) decreases the production and/or concentration of VEGF or other angiogenic or inflammatory mediators or a change in tumor blood flow or metabolism, or peritumoral inflammation or edema in a subject with breast cancer or an animal model with a pre-established human tumor; (ii) reduces or ameliorates the severity of breast cancer and/or a symptom associated therewith in a subject with breast cancer or an animal model with a pre-established human tumor; (iii) reduces the number symptoms and/or the duration of a symptom(s) associated with breast cancer in a subject with breast cancer or an animal model with a pre-established human tumor; (iv) prevents the onset, progression or recurrence of one or more symptoms associated with breast cancer in a subject with breast cancer or an animal model with a pre-established human tumor; (v) prevents the recurrence of a tumor associated with breast cancer in a subject or an animal model; (vi) enhances or improves the therapeutic effect of another therapy in a subject with breast cancer or an animal model with a pre-established human tumor.
In certain embodiments, a Compound or a pharmaceutical composition thereof is administered to a subject in need thereof in accordance with the methods for treating breast cancer provided herein at a dosage and a frequency of administration that results in one or more of the following: (i) regression of a tumor associated with breast cancer and/or inhibition of the progression of a tumor associated with breast cancer in a subject with breast cancer or an animal model with a pre-established human tumor; (ii) reduction in the growth of a tumor or neoplasm associated with breast cancer and/or decreases the tumor size of associated with breast cancer in a subject with breast cancer or an animal model with a pre-established human tumor; (iii) the size of a tumor associated with breast cancer is maintained and/or the tumor does not increase or increases by less than the increase of a similar tumor after administration of a standard therapy as measured by conventional methods available to one of skill in the art, such as MRI, DCE-MRI, PET scan, X-ray, and CT scan; (iv) reduction in the formation of a tumor associated with breast cancer in a subject with breast cancer or an animal model with a pre-established human tumor; (v) eradication, removal, or control of primary, regional and/or metastatic tumors associated with breast cancer in a subject with breast cancer or an animal model with a pre-established human tumor; (vi) a decrease in the number or size of metastases associated with breast cancer in a subject with breast cancer or an animal model with a pre-established human tumor; and/or (vii) reduction in the growth of a pre-established tumor or neoplasm and/or a decrease in the tumor size (e.g., volume or diameter) of a pre-established tumor in a subject with breast cancer or an animal model with a pre-established human tumor.
In certain embodiments, a Compound or a pharmaceutical composition thereof is administered to a subject in need thereof in accordance with the methods for treating breast cancer provided herein at a dosage and a frequency of administration that achieves one or more of the following: (i) inhibition or reduction in pathological VEGF production in the subject; (ii) stabilization or reduction of peritumoral inflammation or edema in a subject; (iii) reduction of the concentration of VEGF or other angiogenic or inflammatory mediators (e.g., cytokines or interleukins) in biological specimens (e.g., plasma, serum, cerebral spinal fluid, urine or other biofluids) from the subject; (iv) reduction of the concentration of P1GF, VEGF-C, VEGF-D, VEGFR-1, VEGFR-2, IL-6 and/or IL-8 in biological specimens (e.g., plasma, serum, cerebral spinal fluid, urine or other biofluids) from the subject; (v) inhibition or reduction in tumor metabolism or perfusion; (vi) inhibition or reduction in angiogenesis or vasculariztion; and/or (vii) an improvement in quality of life as assessed by methods well known in the art, such as questionnaires.
In one aspect, a method for treating breast cancer presented herein involves the administration of a unit dosage of a Compound or a pharmaceutical composition thereof. The unit dosage may be administered as often as determined effective (e.g., once, twice or three times per day, every other day, once or twice per week, biweekly or monthly). In certain embodiments, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of a unit dose of a Compound or a pharmaceutical composition thereof that ranges from about 0.1 milligram (mg) to about 1000 mg, from about 1 mg to about 1000 mg, from about 5 mg to about 1000 mg, from about 10 mg to about 500 mg, from about 100 mg to about 500 mg, from about 150 mg to about 500 mg, from about 150 mg to about 1000 mg, from about 250 mg to about 1000 mg, from about 300 mg to about 1000 mg, or from about 500 mg to about 1000 mg, or any range in between. In some embodiments, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of a unit dose of a Compound or a pharmaceutical composition thereof of about 15 mg, 16, mg, 17 mg, 18 mg, 19 mg, 20 mg, 21, mg, 22 mg, 23 mg, 24 mg, 25 mg, 26 mg, 27 mg, 28 mg, 29 mg, 30 mg or 40 mg. In certain embodiments, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of a unit dose of a Compound or a pharmaceutical composition thereof of about 50 mg, 60 mg, 70 mg, 80 mg, 90 mg, 100 mg, 110 mg, 120 mg, 125 mg, 130 mg, 140 mg, 150 mg, 160 mg, 175 mg, 200 mg, 250 mg, 300 mg, 350 mg, 400 mg, 450 mg, 500 mg, 550 mg, 600 mg, 650 mg, 700 mg, 750 mg, 800 mg, 850 mg, or 900 mg. In some embodiments, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of a unit dose of a Compound or a pharmaceutical composition thereof of at least about 0.1 mg, 1 mg, 5 mg, 10 mg, 20 mg, 30 mg, 40 mg, 50 mg, 60 mg, 70 mg, 80 mg, 90 mg, 100 mg, 110 mg, 120 mg, 125 mg, 130 mg, 140 mg, 150 mg, 175 mg, 200 mg, 250 mg, 300 mg, 350 mg, 400 mg, 450 mg, 500 mg, 550 mg, 600 mg, 650 mg, 700 mg, 750 mg, 800 mg, 850 mg, 900 mg or more. In certain embodiments, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of a unit dose of a Compound or a pharmaceutical composition thereof of less than about 10 mg, less than about 40 mg, less than about 50 mg, less than about 60 mg, less than about 70 mg, less than about 80 mg, less than about 90 mg, less than about 100 mg, less than about 110 mg, less than about 120 mg, less than about 125 mg, less than about 130 mg, less than about 140 mg, less than about 150 mg, less than 160 mg, less than about 175 mg, or less than about 200 mg. In other embodiments, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of a unit dose of a Compound or a pharmaceutical composition thereof of less than about 250 mg, less than about 300 mg, less than about 350 mg, less than about 400 mg, less than about 450 mg, less than about 500 mg, less than about 550 mg, less than about 600 mg, less than about 650 mg, less than about 700 mg, less than about 750 mg, less than about 800 mg, less than about 850 mg, less than about 900 mg, or less than about 1000 mg.
In specific embodiments, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of a unit dose of a Compound or a pharmaceutical composition thereof of about 20 mg to about 250 mg, about 20 mg to about 200 mg, about 40 mg to about 500 mg, about 40 mg to about 200 mg, about 40 mg to about 160 mg, about 40 mg to about 80 mg, about 75 mg to about 500 mg, about 75 mg to about 450 mg, about 75 mg to about 400 mg, about 75 mg to about 350 mg, about 75 mg to about 300 mg, about 75 mg to about 250 mg, about 75 mg to about 200 mg, about 100 mg to about 200 mg, or any range in between. In other specific embodiments, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of a unit dose of a Compound or a pharmaceutical composition thereof of about 15 mg, 20 mg, 35 mg, 40 mg, 50 mg, 60 mg, 75 mg, 80 mg, 100 mg, 125 mg, 150 mg, 160 mg, 175 mg, 200 mg, 225 mg, 250 mg or 300 mg. In some embodiments, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of a unit dose of a Compound or a pharmaceutical composition thereof of about 350 mg, 400 mg, 500 mg, 600 mg, 700 mg, 800 mg, 900 mg, or 1000 mg. In some embodiments, a unit dose of a Compound or a pharmaceutical composition thereof is administered to a subject once per day, twice per day, three times per day; once, twice or three times every other day (i.e., on alternate days); once, twice or three times every two days; once, twice or three times every three days; once, twice, or three times every four days; once, twice or three times every five days; once, twice or three times once a week, biweekly or monthly.
In certain embodiments, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of a unit dose of a Compound or a pharmaceutical composition thereof that ranges from about 20 mg to about 500 mg per day. In some embodiments, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of a unit dose of a Compound or a pharmaceutical composition thereof that ranges from about 40 mg to about 500 mg per day, about 20 to about 200 mg per day, about 80 mg to about 500 mg per day, about 100 mg to about 500 mg per day, about 80 mg to about 400 mg per day, about 80 mg to about 300 mg per day, about 80 mg to about 200 mg per day, about 200 mg to about 300 mg per day, about 200 mg to about 400 mg per day, or any range in between. In a specific embodiment, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of a unit dose of about 20 mg of a Compound or a pharmaceutical composition thereof twice per day. In another specific embodiment, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of a unit dose of about 40 mg of a Compound or a pharmaceutical composition thereof twice per day. In another specific embodiment, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of a unit dose of about 80 mg of a Compound or a pharmaceutical composition thereof twice per day. In another specific embodiment, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of a unit dose of about 100 mg of a Compound or a pharmaceutical composition thereof twice per day. In another specific embodiment, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of a Compound or a pharmaceutical composition at the dosage, frequency of administration and route of administration set forth in the working examples infra in Section 11 et seq.
In some embodiments, a method for treating breast cancer presented herein involves the administration of a dosage of a Compound or a pharmaceutical composition thereof that is expressed as milligram per meter squared (mg/m2). The mg/m2 for a Compound may be determined, for example, by multiplying a conversion factor for an animal by an animal dose in mg/kg to obtain the dose in mg/m2 for human dose equivalent. For regulatory submissions the FDA may recommend the following conversion factors: Mouse=3, Hamster=4.1, Rat=6, Guinea Pig=7.7. (based on Freireich et al., Cancer Chemother Rep. 50(4):219-244 (1966)). The height and weight of a human may be used to calculate a human body surface area applying Boyd's Formula of Body Surface Area. In specific embodiments, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of an amount of a Compound or a pharmaceutical composition thereof in the range of from about 0.1 mg/m2 to about 1000 mg/m2, or any range in between.
Other non-limiting exemplary doses of a Compound that may be used in the methods for treating breast cancer provided herein include milligram (mg) or microgram (μg) amounts per kilogram (kg) of subject or sample weight per day such as from about 0.001 mg per kg to about 1500 mg per kg per day, from about 0.001 mg per kg to about 1400 mg per kg per day, from about 0.001 mg per kg to about 1300 mg per kg per day, from about 0.001 mg per kg to about 1200 mg per kg per day, from about 0.001 mg per kg to about 1100 mg per kg per day, from about 0.001 mg per kg to about 1000 mg per kg per day, from about 0.01 mg per kg to about 1500 mg per kg per day, from about 0.01 mg per kg to about 1000 mg per kg per day, from about 0.1 mg per kg to about 1500 mg per kg per day, from about 0.1 mg per kg to about 1000 mg per kg per day, from about 0.1 mg per kg to about 500 mg per kg per day, from about 0.1 mg per kg to about 100 mg per kg per day, or from about 1 mg per kg to about 100 mg per kg per day. In specific embodiments, oral doses for use in the methods provided herein are from about 0.01 mg to about 300 mg per kg body weight per day, from about 0.1 mg to about 75 mg per kg body weight per day, or from about 0.5 mg to 5 mg per kg body weight per day. In certain embodiments, oral doses for use in the methods provided herein involves the oral administration to a subject in need thereof of a dose of a Compound or a pharmaceutical composition thereof that ranges from about 80 mg to about 800 mg per kg per day, from about 100 mg to about 800 mg per kg per day, from about 80 mg to about 600 mg per kg per day, from about 80 mg to about 400 mg per kg per day, from about 80 mg to about 200 mg per kg per day, from about 200 mg to about 300 mg per kg per day, from about 200 mg to about 400 mg per kg per day, from about 200 mg to about 800 mg per kg per day, or any range in between. In certain embodiments, doses of a Compound that may be used in the methods provided herein include doses of about 0.1 mg/kg/day, 0.2 mg/kg/day, 0.3 mg/kg/day, 0.4 mg/kg/day, 0.5 mg/kg/day, 0.6 mg/kg/day, 0.7 mg/kg/day, 0.8 mg/kg/day, 0.9 mg/kg/day, 1 mg/kg/day, 1.5 mg/kg/day, 2 mg/kg/day, 2.5 mg/kg/day, 2.75 mg/kg/day, 3 mg/kg/day, 4 mg/kg/day, 5 mg/kg/day, 6 mg/kg/day, 6.5 mg/kg/day, 6.75 mg/kg/day, 7 mg/kg/day, 7.5 mg/kg/day, 8 mg/kg/day, 8.5 mg/kg/day, 9 mg/kg/day, 10 mg/kg/day, 11 mg/kg/day, 12 mg/kg/day, 13 mg/kg/day, 14 mg/kg/day or 15 mg/kg/day. In accordance with these embodiments, the dosage may be administered one, two or three times per day, every other day, or once or twice per week and the dosage may be administered orally.
In specific aspects, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of a Compound or a pharmaceutical composition thereof at a dosage that achieves a target plasma concentration of the Compound in a subject with breast cancer or an animal model with a pre-established human tumor (e.g., tumor associated with breast cancer). In a particular embodiment, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of a Compound or a pharmaceutical composition thereof at a dosage that achieves a plasma concentration of the Compound ranging from approximately 0.001 μg/mL to approximately 100 mg/mL, approximately 0.01 μg/mL to approximately 100 mg/mL, approximately 0.01 μg/mL to approximately 10 mg/mL, approximately 0.1 μg/mL to approximately 500 μg/mL, approximately 0.1 μg/mL to approximately 100 μg/mL, approximately 0.1 μg/mL to approximately 10 mg/mL, or approximately 0.5 μg/mL to approximately 10 μg/mL in a subject with breast cancer or an animal model with a pre-established human tumor (e.g., tumor associated with breast cancer). To achieve such plasma concentrations, a Compound or a pharmaceutical composition thereof may be administered at doses that vary from 0.1 μg to 100,000 mg, depending upon the route of administration. In certain embodiments, subsequent doses of a Compound may be adjusted accordingly based on the plasma concentrations of the Compound achieved with initial doses of the Compound or pharmaceutical composition thereof administered to the subject.
In specific aspects, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of a Compound or a pharmaceutical composition thereof at a dosage that achieves a target plasma concentration of VEGF, P1GF, VEGF-C, VEGF-D, IL-6, IL-8, VEGFR-1 and/or VEGFR-2 in a subject with breast cancer or an animal model with a pre-established human tumor (e.g., tumor associated with breast cancer). In a particular embodiment, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of a Compound or a pharmaceutical composition thereof at a dosage that achieves a plasma concentration of VEGF, P1GF, VEGF-C, and/or VEGF-D ranging from approximately 0.1 μg/mL to approximately 100 mg/mL, approximately 0.1 p/mL to approximately 10 mg/mL, approximately 0.1 μg/mL to approximately 1 mg/mL, approximately 0.1 pg/mL to approximately 500 μg/mL, approximately 0.1 pg/mL to approximately 250 μg/mL, approximately 0.1 pg/mL to approximately 100 μg/mL, approximately 0.1 pg/mL to approximately 10 μg/mL, 1 pg/mL to approximately 10 μg/mL, or approximately 4 pg/mL to approximately 10 μg/mL in a subject with breast cancer or an animal model with a pre-established human tumor (e.g., tumor associated with breast cancer). To achieve such plasma concentrations, a Compound or a pharmaceutical composition thereof may be administered at doses that vary from 0.1 pg to 100,000 mg, depending upon the route of administration. In certain embodiments, subsequent doses of a Compound or a pharmaceutical composition thereof may be adjusted accordingly based on the plasma concentrations of VEGF, P1GF, VEGF-C, VEGF-D, IL-6, IL-8, VEGFR-1 and/or VEGFR-2 achieved with initial doses of the Compound or pharmaceutical composition thereof administered to the subject.
In specific aspects, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of a Compound or a pharmaceutical composition thereof at a dosage and/or frequency of administration that achieves an imaging outcome indicating inhibition, stability, and/or reduction in a monitoring parameter such as tumor size, tumor perfusion, tumor metabolism, or peritumoral inflammation or edema, as assessed, e.g., by MRI, DCE-MRI, PET scan, X-ray, and/or CT scan. To achieve such imaging outcome, a Compound or a pharmaceutical composition thereof may be administered at doses that vary from 0.1 pg to 100,000 mg, depending upon the route and/or frequency of administration. In certain embodiments, subsequent doses of a Compound or a pharmaceutical composition thereof may be adjusted accordingly based on the imaging outcome achieved with initial doses of the Compound or pharmaceutical composition thereof administered to the subject, as assessed, e.g., by MRI, DCE-MRI, PET scan, X-ray, and/or CT scan
In particular embodiments, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of a Compound or a pharmaceutical composition thereof at a dosage that achieves the desired tissue to plasma concentration ratios of the Compound as determined, e.g., by any imaging techniques known in the art such as whole-body autoradiography, in a subject with breast cancer or an animal model (such as an animal model with a pre-established human tumor, e.g., a tumor associated with breast cancer). Table 23 lists exemplary tissue to plasma concentration ratios of a Compound as determined by whole-body autoradiography.
In some embodiments, a method for treating breast cancer presented herein involves the administration to a subject in need thereof of one or more doses of an effective amount of a Compound or a pharmaceutical composition, wherein the effective amount may or may not be the same for each dose. In particular embodiments, a first dose of a Compound or pharmaceutical composition thereof is administered to a subject in need thereof for a first period of time, and subsequently, a second dose of a Compound is administered to the subject for a second period of time. The first dose may be more than the second dose, or the first dose may be less than the second dose. A third dose of a Compound may also be administered to a subject in need thereof for a third period of time.
In some embodiments, the dosage amounts described herein refer to total amounts administered; that is, if more than one Compound is administered, then, in some embodiments, the dosages correspond to the total amount administered. In a specific embodiment, oral compositions contain about 5% to about 95% of a Compound by weight.
The length of time that a subject in need thereof is administered a Compound or a pharmaceutical composition in accordance with the methods for treating breast cancer presented herein will be the time period that is determined to be efficacious. In certain embodiments, a method for treating breast cancer presented herein involves the administration of a Compound or a pharmaceutical composition thereof for a period of time until the severity and/or number of symptoms associated with breast cancer decrease. In some embodiments, a method for treating breast cancer presented herein involves the administration of a Compound or a pharmaceutical composition thereof for up to 48 weeks. In other embodiments, a method for treating breast cancer presented herein involves the administration of a Compound or a pharmaceutical composition thereof for up to about 4 weeks, 8 weeks, 12 weeks, 16 weeks, 20 weeks, 24 weeks, 26 weeks (0.5 year), 52 weeks (1 year), 78 weeks (1.5 years), 104 weeks (2 years), or 130 weeks (2.5 years) or more. In certain embodiments, a method for treating breast cancer presented herein involves the administration of a Compound or a pharmaceutical composition thereof for an indefinite period of time. In some embodiments, a method for treating breast cancer presented herein involves the administration of a Compound or a pharmaceutical composition thereof for a period of time followed by a period of rest (i.e., a period wherein the Compound is not administered) before the administration of the Compound or pharmaceutical composition thereof is resumed. In specific embodiments, a method for treating NF presented herein involves the administration of a Compound or a pharmaceutical composition thereof in cycles, e.g., 1 week cycles, 2 week cycles, 3 week cycles, 4 week cycles, 5 week cycles, 6 week cycles, 8 week cycles, 9 week cycles, 10 week cycles, 11 week cycles, or 12 week cycles. In such cycles, the Compound or a pharmaceutical composition thereof may be administered once, twice, three times, or four times daily. In particular embodiments, a method for treating a NF presented herein involves the administration of a Compound or a pharmaceutical composition thereof twice daily in 4 week cycles or 6 week cycles.
In specific embodiments, the period of time of administration of a Compound or pharmaceutical composition thereof may be dictated by one or more monitoring parameters, e.g., concentration of VEGF or other angiogenic or inflammatory mediators (e.g., cytokines or interleukins such as IL-6 or IL-8); tumor size, blood flow, or metabolism; peritumoral inflammation or edema. In particular embodiments, the period of time of administration of a Compound or pharmaceutical composition thereof may be adjusted based on one or more monitoring parameters, e.g., concentration of VEGF or other angiogenic or inflammatory mediators (e.g., cytokines or interleukins such as IL-6 or IL-8); tumor size, blood flow, or metabolism; and/or peritumoral inflammation or edema.
In certain embodiments, in accordance with the methods for treating breast cancer presented herein, a Compound or a pharmaceutical composition thereof is administered to a subject in need thereof prior to, concurrently with, or after a meal (e.g., breakfast, lunch, or dinner). In specific embodiments, in accordance with the methods for treating breast cancer presented herein, a Compound or a pharmaceutical composition thereof is administered to a subject in need thereof in the morning (e.g., between 5 am and 12 pm). In certain embodiments, in accordance with the methods for treating breast cancer presented herein, a Compound or a pharmaceutical composition thereof is administered to a subject in need thereof at noon (i.e., 12 pm). In particular embodiments, in accordance with the methods for treating breast cancer presented herein, a Compound or a pharmaceutical composition thereof is administered to a subject in need thereof in the afternoon (e.g., between 12 pm and 5 pm), evening (e.g., between 5 pm and bedtime), and/or before bedtime.
In specific embodiments, a dose of a Compound or a pharmaceutical composition thereof is administered to a subject once per day, twice per day, three times per day; once, twice or three times every other day (i.e., on alternate days); once, twice or three times every two days; once, twice or three times every three days; once, twice or three times every four days; once, twice or three times every five days; once, twice, or three times once a week, biweekly or monthly.
5.5 Combination Therapy
Presented herein are combination therapies for the treatment of breast cancer which involve the administration of a Compound in combination with one or more additional therapies to a subject in need thereof. In a specific embodiment, presented herein are combination therapies for the treatment of breast cancer which involve the administration of an effective amount of a Compound in combination with an effective amount of another therapy to a subject in need thereof.
As used herein, the term “in combination,” refers, in the context of the administration of a Compound, to the administration of a Compound prior to, concurrently with, or subsequent to the administration of one or more additional therapies (e.g., agents, surgery, or radiation) for use in treating breast cancer. The use of the term “in combination” does not restrict the order in which one or more Compounds and one or more additional therapies are administered to a subject. In specific embodiments, the interval of time between the administration of a Compound and the administration of one or more additional therapies may be about 1-5 minutes, 1-30 minutes, 30 minutes to 60 minutes, 1 hour, 1-2 hours, 2-6 hours, 2-12 hours, 12-24 hours, 1-2 days, 2 days, 3 days, 4 days, 5 days, 6 days, 7 days, 1 week, 2 weeks, 3 weeks, 4 weeks, 5 weeks, 6 weeks, 7 weeks, 8 weeks, 9 weeks, 10 weeks, 15 weeks, 20 weeks, 26 weeks, 52 weeks, 11-15 weeks, 15-20 weeks, 20-30 weeks, 30-40 weeks, 40-50 weeks, 1 month, 2 months, 3 months, 4 months 5 months, 6 months, 7 months, 8 months, 9 months, 10 months, 11 months, 12 months, 1 year, 2 years, or any period of time in between. In certain embodiments, a Compound and one or more additional therapies are administered less than 1 day, 1 week, 2 weeks, 3 weeks, 4 weeks, one month, 2 months, 3 months, 6 months, 1 year, 2 years, or 5 years apart.
In some embodiments, the combination therapies provided herein involve administering a Compound daily, and administering one or more additional therapies once a week, once every 2 weeks, once every 3 weeks, once every 4 weeks, once every month, once every 2 months (e.g., approximately 8 weeks), once every 3 months (e.g., approximately 12 weeks), or once every 4 months (e.g., approximately 16 weeks). In certain embodiments, a Compound and one or more additional therapies are cyclically administered to a subject. Cycling therapy involves the administration of the Compound for a period of time, followed by the administration of one or more additional therapies for a period of time, and repeating this sequential administration. In certain embodiments, cycling therapy may also include a period of rest where the Compound or the additional therapy is not administered for a period of time (e.g., 2 days, 3 days, 4 days, 5 days, 6 days, 7 days, 1 week, 2 weeks, 3 weeks, 4 weeks, 5 weeks, 10 weeks, 20 weeks, 1 month, 2 months, 3 months, 4 months, 5 months, 6 months, 7 months, 8 months, 9 months, 10 months, 11 months, 12 months, 2 years, or 3 years). In an embodiment, the number of cycles administered is from 1 to 12 cycles, from 2 to 10 cycles, or from 2 to 8 cycles.
In some embodiments, the methods for treating breast cancer provided herein comprise administering a Compound as a single agent for a period of time prior to administering the Compound in combination with an additional therapy. In certain embodiments, the methods for treating breast cancer provided herein comprise administering an additional therapy alone for a period of time prior to administering a Compound in combination with the additional therapy.
In some embodiments, the administration of a Compound and one or more additional therapies in accordance with the methods presented herein have an additive effect relative the administration of the Compound or said one or more additional therapies alone. In some embodiments, the administration of a Compound and one or more additional therapies in accordance with the methods presented herein have a synergistic effect relative to the administration of the Compound or said one or more additional therapies alone.
As used herein, the term “synergistic,” refers to the effect of the administration of a Compound in combination with one or more additional therapies (e.g., agents), which combination is more effective than the additive effects of any two or more single therapies (e.g., agents). In a specific embodiment, a synergistic effect of a combination therapy permits the use of lower dosages (e.g., sub-optimal doses) of a Compound or an additional therapy and/or less frequent administration of a Compound or an additional therapy to a subject. In certain embodiments, the ability to utilize lower dosages of a Compound or of an additional therapy and/or to administer a Compound or said additional therapy less frequently reduces the toxicity associated with the administration of a Compound or of said additional therapy, respectively, to a subject without reducing the efficacy of a Compound or of said additional therapy, respectively, in the treatment of breast cancer. In some embodiments, a synergistic effect results in improved efficacy of a Compound and each of said additional therapies in treating breast cancer. In some embodiments, a synergistic effect of a combination of a Compound and one or more additional therapies avoids or reduces adverse or unwanted side effects associated with the use of any single therapy.
The combination of a Compound and one or more additional therapies can be administered to a subject in the same pharmaceutical composition. Alternatively, a Compound and one or more additional therapies can be administered concurrently to a subject in separate pharmaceutical compositions. A Compound and one or more additional therapies can be administered sequentially to a subject in separate pharmaceutical compositions. A Compound and one or more additional therapies may also be administered to a subject by the same or different routes of administration.
The combination therapies provided herein involve administrating to a subject to in need thereof a Compound in combination with conventional, or known, therapies for breast cancer. Current therapies for breast cancer, include surgery, and in some cases radiation or drug therapy such as chemotherapy. Other therapies for breast cancer or a condition associated therewith are aimed at controlling or relieving symptoms, e.g., headaches, inflammation, soreness, and seizures. Accordingly, in some embodiments, the combination therapies provided herein involve administrating to a subject to in need thereof a pain reliever, a medication for seizures, or other therapy aimed at alleviating or controlling symptoms associated with breast cancer or a condition associated therewith.
In specific embodiments, combination therapies provided herein involve administering to a subject in need thereof a Compound in combination with one or more anti-cancer therapies. Specific examples of anti-cancer agents that may be used in combination with a Compound include: a hormonal agent (e.g., aromatase inhibitor, selective estrogen receptor modulator (SERM), and estrogen receptor antagonist), chemotherapeutic agent (e.g., microtubule dissembly blocker, antimetabolite, topisomerase inhibitor, and DNA crosslinker or damaging agent), anti-angiogenic agent (e.g., VEGF antagonist, receptor antagonist, integrin antagonist, vascular targeting agent (VTA)/vascular disrupting agent (VDA)), radiation therapy, and conventional surgery.
Non-limiting examples of hormonal agents that may be used in combination with a Compound include aromatase inhibitors, SERMs, and estrogen receptor antagonists. Hormonal agents that are aromatase inhibitors may be steroidal or nonsteroidal. Non-limiting examples of nonsteroidal hormonal agents include letrozole, anastrozole, aminoglutethimide, fadrozole, and vorozole. Non-limiting examples of steroidal hormonal agents include aromasin (exemestane), formestane, and testolactone. Non-limiting examples of hormonal agents that are SERMs include tamoxifen (branded/marketed as Nolvadex®), afimoxifene, arzoxifene, bazedoxifene, clomifene, femarelle, lasofoxifene, ormeloxifene, raloxifene, and toremifene. Non-limiting examples of hormonal agents that are estrogen receptor antagonists include fulvestrant. Other hormonal agents include but are not limited to abiraterone and lonaprisan.
Non-limiting examples of chemotherapeutic agents that may be used in combination with a Compound include a microtubule disassembly blocker, an antimetabolite, a topisomerase inhibitor, and a DNA crosslinker or damaging agent. Chemotherapeutic agents that are microtubule dissemby blockers include, but are not limited to, taxenes (e.g., paclitaxel (branded/marketed as TAXOL®), docetaxel, abraxane, larotaxel, ortataxel, and tesetaxel); epothilones (e.g., ixabepilone); and vinca alkaloids (e.g., vinorelbine, vinblastine, vindesine, and vincristine (branded/marketed as ONCOVIN®)).
Chemotherapeutic agents that are antimetabolites include, but are not limited to, folate antimetabolites (e.g., methotrexate, aminopterin, pemetrexed, raltitrexed); purine antimetabolites (e.g., cladribine, clofarabine, fludarabine, mercaptopurine, pentostatin, thioguanine); pyrimidine antimetabolites (e.g., 5-fluorouracil, capcitabine, gemcitabine (branded/marketed as GEMZAR®), cytarabine, decitabine, floxuridine, tegafur); and deoxyribonucleotide antimetabolites (e.g., hydroxyurea).
Chemotherapeutic agents that are topoisomerase inhibitors include, but are not limited to, class I (camptotheca) topoisomerase inhibitors (e.g., topotecan (branded/marketed as HYCAMTIN®) irinotecan, rubitecan, and belotecan); class II (podophyllum) topoisomerase inhibitors (e.g., etoposide or VP-16, and teniposide); anthracyclines (e.g., doxorubicin, epirubicin, Doxil, aclarubicin, amrubicin, daunorubicin, idarubicin, pirarubicin, valrubicin, and zorubicin); and anthracenediones (e.g., mitoxantrone, and pixantrone).
Chemotherapeutic agents that are DNA crosslinkers (or DNA damaging agents) include, but are not limited to, alkylating agents (e.g., cyclophosphamide, mechlorethamine, ifosfamide (branded/marketed as IFEX®), trofosfamide, chlorambucil, melphalan, prednimustine, bendamustine, uramustine, estramustine, carmustine (branded/marketed as BiCNU®), lomustine, semustine, fotemustine, nimustine, ranimustine, streptozocin, busulfan, mannosulfan, treosulfan, carboquone, N,N,N-triethylenethiophosphoramide, triaziquone, triethylenemelamine); alkylating-like agents (e.g., carboplatin (branded/marketed as PARAPLATIN®), cisplatin, oxaliplatin, nedaplatin, triplatin tetranitrate, satraplatin, picoplatin); nonclassical DNA crosslinkers (e.g., procarbazine, dacarbazine, temozolomide (branded/marketed as TEMODAR®), altretamine, mitobronitol); and intercalating agents (e.g., actinomycin, bleomycin, mitomycin, and plicamycin).
Non-limiting examples of anti-angiogenic agents that may be used in combination with a Compound include VEGF antagonists, receptor antagonists, integrin antagonists (e.g., Vitaxin®, cilengitide, and S247), and VTAs/VDAs (e.g., fosbretabulin). VEGF antagonists include, but are not to, anti-VEGF antibodies (e.g., bevacizumab (branded/marketed as AVASTIN) and ranibizumab (branded/marketed as LUCENTIS®)), VEGF traps (e.g., aflibercept), VEGF antisense or siRNA or miRNA, and aptamers (e.g., pegaptanib (branded/marketed as MACUGEN®)). Anti-angiogenic agents that are receptor antagonists include, but are not limited to, antibodies (e.g., ramucirumab) and kinase inhibitors (e.g., sunitinib (e.g., branded/marketed as SUTENT®), sorafenib, cediranib, panzopanib, vandetanib, axitinib, and AG-013958) such as tyrosine kinase inhibitors. Other non-limiting examples of anti-angiogenic agents include ATN-224, anecortave acetate (branded/marketed as RETAANE®), microtubule depolymerization inhibitor such as combretastatin A4 prodrug, and recombinant protein or protein fragment such as collagen 18 (endostatin).
Non-limiting examples of other therapies that may be administered to a subject in combination with a Compound include:
Non-limiting examples of other therapies that may be administered to a subject in combination with a Compound include: a synthetic nonapeptide analog of naturally occurring gonadotropin releasing hormone such as leuprolide acetate (branded/marketed as LUPRON®); a nonsteroidal, anti-androgen such as flutamide (branded/marketed as EULEXIN®) or nilutamide (branded/marketed as NILANDRON®); a non-steroidal androgen receptor inhibitor such as bicalutamide (branded/marketed as CASODEX®); steroid hormone such as progesterone; anti-fungal agent such as Ketoconazole (branded/marketed as NIZORAL®); glucocorticoid such as prednisone; estramustine phosphate sodium (branded/marketed as EMCYT®); and bisphosphonate such as pamidronate, alendronate, and risedronate.
Other specific examples of therapies that may be used in combination with a Compound include, but are not limited to, antibodies that specifically bind to a tumor specific antigen or tumor associated antigen, e.g., anti-EGFR/HER-1 antibodies.
Additional specific examples of therapies that may be used in combination with a Compound include, but are not limited to, agents associated with cancer immunotherapy, e.g., cytokines, interleukins, and cancer vaccines.
Specific examples of agents alleviating side-effects associated with breast cancer, that can be used as therapies in combination with a Compound, include, but are not limited to: antiemetics, e.g., Ondansetron hydrochloride (branded/marketed as Zofran®), Granisetron hydrochloride (branded/marketed as Kytril®), Lorazepam (branded/marketed as Ativan®) and Dexamethasone (branded/marketed as Decadron®).
In certain embodiments, combination therapies provided herein for treating breast cancer comprise administering a Compound in combination with one or more agents used to treat and/or manage one or more of the following conditions: bleeding, arterial and venous thrombosis, hypertension, delayed wound healing, asymptomatic proteinuria, nasal septal perforation, reversible posterior leukoencephalopathy syndrome in association with hypertension, light-headedness, ataxia, headache, hoarseness, nausea, vomiting, diarrhea, rash, subungual hemorrhage, myelosuppression, fatigue, hypothyroidism, QT interval prolongation, and heart failure.
In certain embodiments, combination therapies provided herein for treating breast cancer comprise administering a Compound in combination with one or more current anti-angiogenesis agents and one or more agents used to treat and/or manage a side effect observed with one or more of the current anti-angiogenesis agents, such as, bleeding, arterial and venous thrombosis, hypertension, delayed wound healing, asymptomatic proteinuria, nasal septal perforation, reversible posterior leukoencephalopathy syndrome in association with hypertension, light-headedness, ataxia, headache, hoarseness, nausea, vomiting, diarrhea, rash, subungual hemorrhage, myelosuppression, fatigue, hypothyroidism, QT interval prolongation, or heart failure.
In certain embodiments, a Compound is not used in combination with a drug that is primarily metabolized by CYP2D6 (such as an antidepressant (e.g., a tricyclic antidepressant, a selective serotonin reuptake inhibitor, and the like), an antipsychotic, a beta-adrenergic receptor blocker, or certain types of anti-arrhythmics) to treat breast cancer. In other embodiments, a Compound is not used in combination with a drug that is primarily metabolized by CYP2D6 (such as an antidepressant (e.g., a tricyclic antidepressant, a selective serotonin reuptake inhibitor, and the like), an antipsychotic, a beta-adrenergic receptor blocker, or certain types of anti-arrhythmics) to treat breast cancer.
In certain embodiments, a Compound is used in combination with letrozole (marketed/branded as FERMARA®) to treat breast cancer. In other embodiments, a Compound is not used in combination with letrozole (marketed/branded as FERMARA®) to treat breast cancer.
The following examples are presented by way of illustration not limitation.
Methods for preparing certain Compounds provided herein and the Compounds disclosed on pages 26 to 98 of the '764 publication are provided on pages 112 to 142 of the '764 publication and are incorporated by reference herein on pages 99 to 105 and in their entireties and for all purposes. Methods for preparing certain Compounds provided herein and the Compounds disclosed in copending U.S. Provisional Patent Application 61/181,652, entitled: PROCESSES FOR THE PREPARATION OF SUBSTITUTED TETRAHYDRO BETA-CARBOLINES, filed May 27, 2009, are provided therein and are incorporated by reference herein in their entirety and for all purposes.
The following example illustrates how Compound #10 may be formulated for oral administration.
For clinical use, Compound #10 has been formulated using cGMPs. Compound #10 is intended for oral administration and is provided in size 00 color coded, hard gelatin capsules. As shown in Table 2, each capsule contains 2 mg (white), 10 mg (gray), or 20 mg (orange) of the Compound formulated by w/w % (weight/weight %) in a SEDDS or SMEDDS system. The formulated product in the capsules appears as an opaque, off white soft solid at room temperature. If warmed, the encapsulated system begins to soften at temperatures of 38 to 40° C. and eventually becomes a clear, yellow liquid at >44° C.
The ability of the Compounds to modulate hypoxia-inducible endogenous VEGF expression may be analyzed as follows. VEGF protein levels may be monitored by an ELISA assay (R&D Systems). Briefly, HeLa cells may be cultured for 24-48 hours under hypoxic conditions (1% O2, 5% CO2, balanced with nitrogen) in the presence or absence of a Compound. The conditioned media may then be assayed by ELISA, and the concentration of VEGF calculated from the standard ELISA curve of each assay.
A dose-response analysis may be performed using the ELISA assay and conditions described above. The conditions for the dose-response ELISA are analogous to those described above. A series of, e.g., seven different concentrations may be analyzed. In parallel, a dose-response cytotoxicity assay may be performed using Cell Titer Glo (Promega) under the same conditions as the ELISA to ensure that the inhibition of VEGF expression was not due to the cytotoxicity. Dose-response curves may be plotted using percentage inhibition versus concentration of the Compound, and EC50 and CC50 values may be generated for each Compound with the maximal inhibition set as 100% and the minimal inhibition as 0%. In one embodiment, Compounds will have an EC50 of less than 50, less than 10, less than 2, less than 0.5, or less than 0.01.
The EC50 for a series of Compounds is provided in Table 3.
LC/MS for certain Compounds was performed on either a Waters 2795 or 2690 model separations module coupled with a Waters Micromass ZQ mass spectrometer using a Waters Xterra MS C18 4.6×50 mm reverse phase column (detection at 254 nM). The methods employed a gradient of acetonitrile (ACN) in water at 2 mL/min at ambient temperature as shown in Table 3a. The mobile phase was buffered with a 0.1 N formic acid.
The standard 6 minute method maintains a constant 85/5/10 ratio of water/ACN/1% aqueous formic acid from 0 minutes to 0.5 minutes. The method runs a linear gradient from 85/5/10 at 0.5 minutes to 0/90/10 at 3.5 minutes. The method holds at 0/90/10 until 4.5 minutes then immediately drops back down to 85/5/10 and holds there until 6 minutes.
The non-polar 6 minute method maintains a constant 60/30/10 ratio of water/ACN/1% aqueous formic acid from 0 minutes to 0.5 minutes. The method runs a linear gradient from 60/30/10 at 0.5 minutes to 0/90/10 at 3.5 minutes. The method holds at 0/90/10 until 4.5 minutes then immediately drops back down to 60/30/10 and holds there until 6 minutes.
The polar 6 minute method maintains a constant 90/0/10 ratio of water/ACN/1% aqueous formic acid from 0 minutes to 0.5 minutes. The method runs a linear gradient from 90/0/10 at 0.5 minutes to 20/70/10 at 3.5 minutes. The method holds at 20/70/10 until 4.5 minutes then immediately drops back down to 90/0/10 and holds there until 6 minutes.
LC/MS for Compounds 1611 and 1669 was performed using a C18-BDS 5 (250×4.6 mm) column with a 0.7 mL/min flow rate. The following solvent gradient was employed using 0.1% TFA/water as solvent A and acetonitrile as solvent B: 20% B for 0-20 minutes, 70% B for 20-30 minutes, 100% B for 30-40 minutes, 20% B for 40-50 minutes.
The examples that follow demonstrate that the Compounds tested can inhibit the pathological production of human VEGF, and suppress edema, inflammation, pathological angiogenesis and tumor growth tumor growth. Compounds tested have been shown to inhibit the pathological production of human VEGF by multiple human tumor cells and/or human tumors in animal models with pre-established human tumors.
9.1 Inhibition of Pathological Production of VEGF
9.1.1 Cell Based Assays
This example demonstrates the selective inhibition of Compound #10 and Compound 1205 on pathological VEGF production in transformed HeLa cells grown under stressed conditions while sparing VEGF production in HeLa cells grown under non-stressed conditions.
Experimental Design. HeLa (human cervical carcinoma) cell cultures were established under normoxic conditions (21% oxygen). HeLa cells increase VEGF production 4- to 5-fold in response to hypoxia. In one experimental design, vehicle (0.5% DMSO) alone, or a range of concentrations of Compound #10 was added to the HeLa cell cultures and the cells were incubated for 48 hours under either hypoxic (1% oxygen) or normoxic conditions. In another experimental design, vehicle (0.5% DMSO) alone, or a range of concentrations of Compound #10, Compound 1205, or Compound 1330 was added to the culture medium and the cells were incubated for 48 hours. At the completion of treatment, the conditioned media were collected and the VEGF protein levels were assayed in an enzyme-linked immunosorbent assay (ELISA) with primary antibodies that recognize the soluble VEGF121 and VEGF165 isoforms (R & D Systems, Minneapolis, Minn., USA). To ensure that decreases in VEGF concentration were not due to cytotoxicity, cultures were assayed using a standard assay (CELLTITER-GLO® Luminescent Cell Viability Assay; Promega, Madison, Wis., USA) that measures total cellular adenosine triphosphate (ATP) concentrations as an indicator of cell viability.
Results.
This example demonstrates the inhibition of Compound #10 is selective for the pathological production of soluble VEGF isoforms in nontransformed keratinocytes grown under stressed conditions and does not affect the production of soluble VEGF isoforms in nontransformed keratinocytes grown under non-stressed conditions.
Experimental Design. Nontransformed normal human keratinocyte cell cultures were established under normoxic conditions (21% oxygen). Vehicle (0.5% DMSO) alone, or a range of concentrations of Compound #10 was added to the cultures and the cells were incubated for 72 hours under either under hypoxic (1% oxygen) or normoxic conditions. At the completion of treatment, cells were assessed for viability with an ATP assay and conditioned media were evaluated for VEGF protein levels by ELISA (as described in Section 9.1.1.1).
Results.
This data indicates that Compound #10 selectively inhibits or reduces pathological production of soluble VEGF isoforms in nontransformed keratinocytes grown under stressed hypoxic conditions while sparing physiological VEGF production of the same isoforms in unperturbed cells.
This example demonstrates that Compound #10 inhibits the pathological production of matrix bound/cell associated VEGF189 and VEGF206 isoforms resulting from oncogenic transformation.
Experimental Design. HT1080 (human fibrosacoma) cell cultures were established under normoxic conditions (21% oxygen). HT1080 cells constitutively overproduce VEGF even under normoxic conditions. Vehicle (0.5% DMSO) alone or a range of concentrations of Compound #10 was added to the cultures, and the cells were incubated for 48 hours under normoxic conditions. At the completion of treatment, the cells were washed and harvested. Cells were incubated with a primary antibody that recognizes the VEGF189 and VEGF206 isoforms. Infrared-dye labeled antibodies were applied secondarily, and the amounts of VEGF189 and VEGF206 were determined using the IN-CELL WESTERN® assay and ODYSSEY® infrared imaging system (Li-Cor, Lincoln, Nebr., USA); results are expressed as percentage inhibition relative to vehicle treated controls. Conventional Western blotting using the same primary antibody was also performed to confirm the presence of the matrix associated isoforms; for these experiments actin was used as a loading control. Actin is a ubiquitous housekeeping protein that is not known to be post transcriptionally regulated.
Results. As shown in
This data shows that Compound #10 inhibits pathological production of the matrix bound/cell associated VEGF isoforms resulting from oncogene transformation.
This example demonstrates that Compound #10 inhibits soluble VEGF production in multiple human tumor cell lines.
Study Design. The activity of Compound #10 in suppressing VEGF production in a number of other human tumor cell lines has been assessed. These evaluations focused on cell lines that produce sufficient soluble VEGF (>200 pg/mL in conditioned media, either constitutively or under hypoxic stress) to allow assessment of Compound #10 activity by ELISA. In these experiments, cultures were established under normoxic conditions (21% oxygen). Cultures were then incubated for 48 hours with vehicle (0.5% DMSO) alone or with Compound #10 over a range of concentrations from 0.1 nM to 10 μM. Cells requiring induction of VEGF production were incubated under hypoxic conditions (1% oxygen). At the completion of treatment, the conditioned media were collected and assayed by ELISA (as described in Section 9.1.1.1) for soluble VEGF121 and VEGF165 isoforms; results were calculated as percentage inhibition relative to vehicle treated controls. EC50 values were calculated from the dose concentration response curves.
Results. Compound #10 potently inhibited the production of soluble VEGF in 18 of the human tumor cell lines tested to date. The EC50 values for cell lines showing VEGF inhibition are generally in the low nanomolar range, as presented in Table 4. Compound #10 did not show activity in several cell lines in which there was insufficient basal or inducible production of soluble VEGF. Other human cell lines that produce sufficient soluble VEGF in vitro or in vivo may be used, with appropriate adaptations, by those skilled in the art to measure inhibition of pathologically produced soluble human VEGF.
aCell lines requiring incubation under hypoxic conditions (1% oxygen) to induce VEGF production.
9.1.2 Animal Model Systems
This example demonstrates that Compound #10 selectively inhibits pathological VEGF production relative to other human angiogenic factors.
Experimental Design. In a series of experiments evaluating the effects of Compound #10 on intratumoral VEGF and tumor growth, intratumoral levels of VEGF-C, P1GF (Placental Growth Factor), FGF-2 (Fibroblast growth factor 2), survivin, PDGF (Platelet derived growth factor), and endostatin were also measured to assess the selectivity of Compound #10. VEGF-C and P1GF were analyzed to determine the in vivo effects of Compound #10 on other members of the VEGF family of angiogenic factors. All of these factors can be produced at tumor sites, and all may support tumor growth and metastases. See Yoon et al., Circ Res. 2003, 93(2):87 90; Ferrara et al., Nat. Rev. Drug Discov. 2004, 3(5):391 400; Luttun et al., Biochim. Biophys. Acta 2004,1654(1):79 94; Saharinen et al., Trends Immunol. 2004, 25(7):387 95. There is also evidence that VEGF-A may stimulate production of P1GF by a post transcriptional mechanism. See Yao et al., FEBS Lett. 2005, 579(5):1227 34. VEGF-B was not assessed. The angiogenic growth factor FGF-2 was analyzed because it promotes tumor survival (see Bikfalvi et al., Angiogenesis 1998, 1(2):155 73), and has a 5′-UTR IRES. See Vagner at al., Mol. Cell. Biol. 1995, 15(1):35 44; Hellen et al., Genes Dev. 2001, 15(13):1593 612. The survivin protein was similarly evaluated because the survivin mRNA has an IRES. PDGF was assessed because this protein has angiogenic activity and its mRNA contains an IRES. See Sella et al., Mol. Cell. Biol. 1999, 19(8):5429 40; Hellen et al., supra. Endostatin was included because antiangiogenic treatment in vivo has shown that compensatory decreases in endogenous angiogenic inhibitors such as endostatin, thrombospondin, and angiostatin, results in a more pro angiogenic environment. See Sim, Angiogenesis, 1998, 2(1):37-48.
In all of these experiments, HT1080 cells (5×106 cells/mouse) were implanted subcutaneously in male athymic nude mice. When tumors had become established, mice were divided into groups (10 mice/group). Treatments comprised Compound #10 (either alone or as the racemic mixture) or the corresponding vehicle alone, administered by oral gavage BID (“bis in die”; twice a day) on Monday through Friday and QD (“quaque die”; daily) on Saturday and Sunday over periods of 7 to 21 days (Table 5). Tumor size was measured by calipers at the beginning and end of treatment. At the completion of Compound administration, the mice were sacrificed, and excised tumors were assayed by ELISA for intratumoral VEGF or other angiogenic factors using methods analogous to those described in Section 9.1.1.1.
Results. As summarized in the studies shown in Table 5, Compound #10 universally inhibited the production of intratumoral VEGF A and tumor size. Compound #10 also reduced intratumoral P1GF in the experiments where this factor was measured; the results show a variable effect on VEGF-C. Compound #10 did not have statistically significant effects on levels of the other proteins tested, except for FGF 2 levels (as shown in Study 5). In Study 5, treatment was initiated when the tumors were quite large (˜600 mm3). The study was continued for 15-days, and the tumors had become quite bulky by the time intratumoral protein levels were analyzed. However, Compound #10 still decreased intratumoral VEGF levels by 78%, although FGF-2 levels were noted to be significantly elevated at the time of study termination. In Studies 2 and 3, endostatin levels were depressed by 22 to 30%, although these changes were not statistically significant. Collectively, these data indicate that Compound #10 is selective for suppression of VEGF family proteins.
−58*g
−34*h
−63*h
aSome animals received racemic mixture; the dose is expressed as amount of Compound #10 in the mixture.
bMice were treated with 5 mg/kg for the first 9 days and with 50 mg/kg for the last 6 days.
cTreatments were administered by oral gavage BID on Monday through Friday and QD on Saturday and Sunday for the number of days shown. All morning doses were given before 0830 hours. Evening doses were administered after 1630 hours (i.e., ≧8 hours after the morning dose).
dTreatments were administered by oral gavage QD in the morning before 0830 hours on Monday through Friday for the number of days shown.
eVehicle was 35% Labrasol, 35% Labrafac and 30% Solutol).
fCalculated as [1-(treated/control)] × 100%
gDifference in tumor size is shown for Day 14, the day the vehicle-treated mice were taken off study.
hDifference in tumor size is shown for Day 10, the day the vehicle-treated mice were taken off study.
iSix mice per group in Compound #10-treated and vehicle-treated groups were analyzed
This example demonstrates that Compound #10 dose-dependently reduces intratumoral and pathologically produced plasma human VEGF concentrations in vivo.
Experimental Study Design. HT1080 cells (5×106 cells/mouse) were implanted subcutaneously in male athymic nude mice. When tumors had become established (i.e., the mean tumor size had reached 180±75 mm3), mice were divided into 6 groups and treatment was assigned as shown in Table 6.
aTreatments were administered by oral gavage 7-days per week (except the 10-mg-QD regimen, which was administered daily on Monday through Friday) for a total of 18 days. All morning doses were given before 0830 hours. For BID schedules, evening doses were administered after 1630 hours (i.e., ≧8 hours after the morning dose).
bVehicle was L21 (35% Labrasol, 35% Labrafac, and 30% Solutol).
Tumor size was measured using calipers at periodic intervals during the study (data shown in Section 9.2.2). Retro-orbital blood collection was performed to assess Compound #10 trough plasma concentrations after the first dose (just prior to the second dose) on Day 1, Day 4, and Day 9, and at study termination. The study was ended after 18 days, when the vehicle treated tumors reached a mean volume of ˜1755 mm3. Retro-orbital terminal bleeding was performed at ˜8 to 16 hours (depending upon the schedule of Compound administration) after the last dose to assess pathologic plasma human VEGF concentrations and trough Compound #10 plasma concentrations. Mice were sacrificed, and excised tumors were homogenized in buffer containing protease inhibitors. Both terminal intratumoral and pathologic plasma human VEGF levels were measured using an ELISA that recognizes human VEGF121 and VEGF165 (as described in Section 9.1.1.1). Intratumoral VEGF levels were normalized to the total tumor protein concentration, while pathologic plasma human VEGF levels were expressed in pg/mL of plasma. Plasma Compound #10 concentrations were evaluated by high performance liquid chromatography and with tandem mass spectroscopy (HPLC-MS/MS).
Results. As shown in
The data shows that Compound #10 dose-dependently reduces intratumoral and pathologically produced plasma human VEGF concentrations in vivo.
This example demonstrates that Compound 1205 reduces intratumoral and pathologically produced plasma human VEGF concentrations in vivo.
Experimental Design. HT1080 cells (5×106 cells/mice) were implanted subcutaneously into male athymic nude mice. Treatment with vehicle alone or Compound 1205 was initiated when the median tumor volume was approximately 311±88 mm3. Table 7 and Table 9 (study design #21 and #23) provide the study design for assessing tumor and plasma pathologic VEGF concentrations—each group in each study included eight (8) mice. When the tumors in vehicle-treated mice had reached the target size of ˜1200 mm3 for study #21 and ˜1500 mm3 for study #23, all mice in the study were sacrificed, and excised tumors were homogenized in buffer containing protease inhibitors. Both intra-tumor and pathologic plasma human VEGF levels were measured using an ELISA that recognizes human VEGF121 and VEGF165. Intra-tumor VEGF levels were normalized to the total tumor protein concentration and pathologic plasma VEGF levels were expressed in pg/mL. Because smaller tumors produce less VEGF per mg of tumor protein, intra-tumor VEGF levels were normalized to tumor size. Table 9 provides the study design for assessing tumor and pathologic plasma VEGF.
Results. Treatment with Compound 1205 at 0.5 or 3 mg/kg for 14-days significantly reduced the levels of pathologic human VEGF measured in excised tumors (FIG. 27A-B) and in plasma (
9.2 Inhibition of Pathological Angiogenesis and Tumor Growth
9.2.1 Compound #10 Inhibits Tumor Angiogenesis
This example demonstrates that Compound #10 reduces the total volume and diameter of tumor vessels.
Experimental Design. HT1080 cells (5×106 cells/mouse) were implanted subcutaneously in male athymic nude mice. At a mean tumor size of 285±45 mm3, mice were divided into 2 groups and treatment was administered as shown in Table 8.
At the end of treatment, the mice were sacrificed. Excised tumors were assayed by ELISA for VEGF content as described in Section 9.1.1.1, and were sectioned and immunostained with an anti murine CD31 antibody that is specific for endothelial cells.
5c
aTreatments were administered by oral gavage BID on Monday through Friday and QD on Saturday and Sunday Treatments were administered by oral gavage BID on Monday through Friday and QD on Saturday and Sunday for a total of 10 days. All morning doses were given before 0830 hours. Evening doses were administered after 1630 hours (i.e., ≧8 hours after the morning dose).
bVehicle was 5% DMSO and 95% PEG 300.
cRacemic material was used for this study at a dose of 10 mg/kg (1.25 mg/mL), resulting in a dose of the active Compound #10 enantiomer of 5 mg/kg (0.625 mg/mL).
Results. Treatment with Compound #10 resulted in a mean 95% inhibition of tumor VEGF concentration. As shown in
9.2.2 Compound #10 Inhibits Tumor Growth In Vivo
This example demonstrates that Compound #10 inhibits tumor growth in nude mice bearing HT1080 xenografts.
Experimental Design. The experimental design was reported in Section 9.1.2.2.
Results. The dose response effect of Compound #10 that correlated with decreases in tumor and pathologic human VEGF concentrations (see
9.2.3 Compound 1205 Inhibits Tumor Growth In Vivo
This example demonstrates that Compound 1205 inhibits tumor growth in nude mice bearing HT1080 xenografts.
Experimental Design. HT1080 cells (5×106 cells/mouse) were implanted subcutaneously in male athymic nude mice. When tumors had become established (i.e., the mean tumor size had reached 311±88 mm3), mice were divided into 5 groups and treatment was administered as shown in Table 9 and 10. Compound 1330 is a relatively inactive (R,S) diastereomer of Compound 1205, which has (S,S) configuration. For comparison, Compound #10 was included in this study.
Results. The results of the studies described in Table 10 and are shown in
ASee Table 9 for additional study information.
B% Difference in the rat of growth in compound-treated vs. vehicle-treated
CAverage time on study.
9.2.4 Time-Course Effects of Compound #10 on Tumor Size and Pathologically Produced Plasma Human VEGF Concentrations
This example demonstrates that Compound #10 has a rapid onset for reducing xenograft tumor size and pathologically produced plasma human VEGF concentration.
Experimental Design. HT1080 cells (5×106 cells/mouse) were implanted subcutaneously in male athymic nude mice. When tumors had become established (i.e., the mean tumor size had reached 585±150 mm3), mice were divided into 4 treatment groups, as shown in Table 11.
aTreatments were initiated on Day 0 with 20 mice per group. On each day, 5 mice were sacrificed per group for analysis. Mice were treated with Compound #10 daily. Mice were treated with doxorubicin or bevacizumab on Day 0 only.
bVehicle was L21 (35% Labrasol, 35% Labrafac, and 30% Solutol).
Tumor size was measured by calipers immediately pre-treatment and at the time of sacrifice on Day 1, 2, or 3 (5 mice per group per day). At sacrifice, the plasma was collected for assay of pathologic human VEGF concentration using an ELISA that recognizes human VEGF121 and VEGF165 (as described in Section 9.1.1.1).
Results.
9.2.5 Compound #10 Shows Antitumor Activity in Several Human Tumor Xenograft Models
This example demonstrates that Compound #10 shows antitumor activity in several clinically relevant human tumor xenograft models.
Investigators at the National Cancer Institute (NCI) have shown that compounds that inhibit tumor growth in multiple nonclinical models are more likely to have clinical efficacy. See Johnson et al., Br. J. Cancer 2001, 84(10):1424 31. In each of these studies, human tumor cells were implanted and treatment was initiated some days later, only after tumors had developed a vasculature (i.e., when tumors were >100 mm3). This method of waiting to begin treatment until after tumors are established is considered a more stringent and clinically relevant assessment of efficacy compared to beginning treatment immediately after tumor implantation. See Teicher, ed. Totowa, Tumor models in cancer research. Humana Press, 2002: 593-616.
This example demonstrates that Compound #10 shows antitumor activity in an T47D estrogen-sensitive breast cancer xenograft model.
Experimental Design. Estrogen pellets (0.72 mg/pellet) were implanted 30 days prior to cell implantation and again 60 days later. T47D estrogen-sensitive breast cancer cells (5×106 cells/mouse mixed 1:1 with Matrigel™) were implanted subcutaneously in female athymic nude mice. After 31 days, when the tumors had become established (i.e., the mean tumor size had reached 180±33 mm3), mice were divided into 3 treatment groups, and treatment was administered as shown in Table 12. Tamoxifen was included as a positive control.
aTreatments were administered by oral gavage QD.
bVehicle was L21 (35% Labrasol, 35% Labrafac, and 30% Solutol).
Tumor size was measured by calipers at periodic intervals. After 74 days of treatment, the mice were sacrificed. The tumors were not analyzed for intratumoral VEGF levels because of their small size at sacrifice.
Results. Results by treatment regimen are shown in Table 13. In this breast cancer xenograft model, Compound #10 resulted in a transient reduction and persistent delay in tumor growth relative to controls. Compound #10 appeared as active as tamoxifen in suppressing growth of this estrogen-sensitive cell line. In observing the animals, there was no evidence of toxicity associated with Compound #10 treatment.
aDay 74 was the day on which mice were sacrificed.
bVehicle was L21 (35% Labrasol, 35% Labrafac, and 30% Solutol).
This example demonstrates that Compound #10 shows antitumor activity in an MDA-MB-468 estrogen-insensitive breast cancer xenograft model.
MDA-MB-468 estrogen-insensitive breast cancer cells (5×106 cells/mouse mixed 1:1 with Matrigel™) were implanted subcutaneously in female athymic nude mice. After 6 days, tumors had become established (i.e., the mean tumor size had reached 185±26 mm3), mice were divided into 2 treatment groups, and treatment was administered as shown in Table 14.
aTreatments were administered QD continuously by oral gavage for at least 30 days.
bVehicle was L21 (35% Labrasol, 35% Labrafac, and 30% Solutol).
Tumor size was measured by calipers at periodic intervals. When the individual tumor size in a mouse exceeded 1500 mm3, that mouse was sacrificed and both tumor and plasma were assayed for pathologic VEGF concentration as described in Section 9.1.1.1.
Results. Results by treatment regimen are shown in Table 15. Compound #10 at 10 mg/kg significantly reduced intratumoral and plasma pathologic VEGF concentrations on the day on which the animals were sacrificed (range, Day 33 to 53) relative to controls (range, Day 9 to 15). In addition, Compound #10 reduced tumor size and prolonged the time to tumor progression (i.e., the time to reach ≧1000 mm3). In observing the animals, there was no evidence of toxicity associated with Compound #10 treatment.
aTreatments were administered QD continuously by oral gavage for at least 30 days.
bVehicle treated animal tumors reached ≧1500 mm3 between Day 9 and 15 and all vehicle treated animals were sacrificed by Day 15.
cVehicle was L21 (35% Labrasol, 35% Labrafac, and 30% Solutol).
This example shows that Compound #10 reduces tumor perfusion as assessed by dynamic contrast-enhanced magnetic resonance imaging.
Experimental Design. Dynamic contrast-enhanced magnetic resonance imaging can be used preclinically and clinically to evaluate the anatomy of soft tissues, including the identification and accurate measurement of tumor volumes. In addition, evaluation of the intratumoral pharmacokinetics of contrast agents containing gadolinium can be used to measure vascular permeability characteristics. Coupling gadopentetate dimeglumine gadolinium to a small molecule like bovine serum albumin can reveal information about the necrotic (non-perfused) and non-necrotic (perfused) tumor volumes, and the percentage of vascular blood volume relative to the perfused tumor volume (known as the fractional blood volume [fBV]). Use of a macromolecular tracer, gadopentetate dimeglumine, can reveal information regarding the volume transfer coefficient (Ktrans), a variable that represents a combination of vascular permeability, vascular surface area, and blood flow.
MDA MB 468 breast cancer cells (5×106 cells/mouse mixed 1:1 with Matrigel™) were implanted subcutaneously in female athymic nude mice. After 13 days, when the tumors had become established (i.e., the mean tumor size reached ˜400 mm3), mice were divided into 2 treatment groups, and treatment was administered as shown in Table 16.
aVehicle was L21 (35% Labrasol, 35% Labrafac, and 30% Solutol).
Before each DCE-MRI scan, mice were injected intravenously with gadolinium-containing contrast dyes (bovine serum albumin-gadopentetate dimeglumine conjugate at ˜0.03 mmol/kg followed by gadopentetate dimeglumine at ˜0.2 mmol/kg). Baseline DCE-MRI measurements were taken on Day −1, test Compounds were administered on Day 0 through Day 5, and additional DCE-MRI measurements were taken on Days 1, 3, and 5. Image analyses were conducted with customized software. Total tumor volumes were measured by semi-automatically segmenting a region of interest around an anatomical image of the tumor. Tumor volumes of necrotic and non-necrotic tissues were measured by applying the same semi-automated segmentation process to a contrast dyed image. fBV and Ktrans were computed using a standard Kety PK model.
Results. As shown in
As shown in
Conversely, as shown in
Tissue regions identified as necrotic have no measurable vascular permeability, limiting analysis of fBV to non-necrotic tumor regions (primarily in the tumor rim). As shown in
As for fBV, analysis of Ktrans was necessarily confined to non-necrotic tissue. As shown in
This example demonstrates that Compound #10 shows antitumor activity in an SY5Y neuroblastoma xenograft model.
Experimental Design. SY5Y cells are derived from a human neuroblastoma, a childhood tumor arising in neural crest cells. SY5Y cells (1×107 cells/mouse) were implanted subcutaneously in male athymic nude mice. After 7-days, tumors had become established (i.e., the mean tumor size had reached 387±10 mm3), mice were divided into 2 groups, and treatment was administered as shown in Table 17.
aTreatments were administered by oral gavage 5 days per week (Monday through Friday) for up to 50 days.
bVehicle was L22 (35% Labrafil, 35% Labrafac, and 30% Solutol).
Tumor size was measured by calipers at periodic intervals. When the average tumor size in a group exceeded 2000 mm3, the mice in the group were sacrificed and excised tumors were assayed for intratumoral VEGF concentration as described in Section 9.1.1.1. Animals in which tumors did not reach 2000 mm3 were sacrificed at Day 50.
Results. Results by treatment regimen are shown in Table 18. Compound #10 treatment was associated with a significant reduction in mean intratumoral VEGF concentration and essentially eliminated any increase in mean tumor size through 15-days of dosing, substantially prolonging the mean time until tumor progression (tumor size ≧1000 mm3). In contrast, tumors in many control animals exceeded 2000 mm3 by Day 17 and these animals had to be sacrificed. In view of the dramatic effect of Compound #10 treatment, Compound #10 treatment was stopped on Day 15 to determine whether these effects might be sustained after treatment withdrawal. Tumors from mice treated with Compound #10 continued to be smaller than tumors from vehicle treated mice, even after 28-days without treatment (data not shown). At Day 43, treatment with vehicle or Compound #10 was reinitiated for a further 6 days. There were not enough vehicle mice remaining in the study to assess if Compound #10 would be more effective than vehicle in terms of tumor growth inhibition after treatment reinitiation. However, as summarized in Table 18, even after the cessation of treatment for 28-days and then continued Compound #10 treatment for 6 days, intratumoral levels of VEGF were almost completely suppressed in the treated tumors. In observing the animals, there was no evidence of toxicity associated with Compound #10 treatment.
aTreatments were administered by oral gavage 5 days per week (Monday through Friday) for up to 50 days.
bDay 17 was day on which vehicle treated animal tumors had reached ≧2000 mm3 and the mice were sacrificed.
cVehicle was L22 (35% Labrafil, 35% Labrafac, and 30% Solutol).
This example demonstrates that Compound #10 shows antitumor activity in an LNCaP prostate cancer xenograft model.
Experimental Design. The LNCaP cell line is derived from a lymph node metastasis. LNCaP cells (1×106 cells/mouse mixed 1:1 with Matrigel™) were implanted subcutaneously in male athymic nude mice. After 43 days, tumors had become established (i.e., the mean tumor size had reached 260±35 mm3), mice were divided into 2 treatment groups, and treatment was administered as shown in Table 19.
aTreatments were administered M-W-F by oral gavage for at least 35 days.
bVehicle was L21 (35% Labrasol, 35% Labrafac, and 30% Solutol).
Tumor size was measured by calipers at periodic intervals during the study. When the mean tumor size in a mouse exceeded 1500 mm3, mice in that group were sacrificed and both tumor and plasma were assayed for pathologic VEGF concentration as described in Section 9.1.1.1.
Results. Results by treatment regimen are shown in Table 20. Relative to controls, Compound #10 at 10 mg/kg M-W-F reduced intratumoral VEGF concentrations adjusted for tumor size on the day on which the animals were sacrificed. In addition, Compound #10 prolonged the time to tumor progression (i.e., the time to reach ≧1000 mm3). In observing the animals, there was no evidence of toxicity associated with Compound #10 treatment.
aTreatments were administered M-W-F by oral gavage for at least 35 days.
bVehicle treated animal tumors reached ≧1500 mm3 by ~Day 30 and all vehicle-treated animals were sacrificed by Day 35.
cVehicle was L21 (35% Labrasol, 35% Labrafac, and 30% Solutol).
dAdjusted for tumor size
This example demonstrates that Compound #10 shows antitumor activity in orthotopic SY5Y neuroblastoma and SKNEP Ewing sarcoma tumor models.
Experimental Design. In orthotopic tumor models, human tumor cells are implanted into the mouse in an organ that corresponds to the location from which the tumors arise. Such models may provide a better predictor of clinical efficacy than injection of tumors into the flanks of nude mice. See Hoffman, ° Invest. New Drugs 1999, 17(4):343-59. SY5Y neuroblastoma or SKNEP Ewing sarcoma tumor cells (1×106 cells/mouse) were implanted into the kidney capsule of female athymic nude mice according to published methods. See Huang et al., Proc. Natl. Acad. Sci. USA 2003, 100(13):7785-90. One week after implantation of each type of tumor, mice were divided into 2 groups and were administered a test Compound as shown in Table 21.
aTreatments were administered by oral gavage 5 days per week (Monday through Friday) for up to 5 weeks.
bVehicle was L3 (70% Labrasol, 18.3% Labrafac, and 11.7% Labrafil).
After 5 weeks of treatment, the mice were sacrificed, and the weights of the tumors were assessed.
Results. As shown in
9.2.6 Compound #10 Penetrates Disease Relevant Tissues
This example demonstrates that Compound #10 penetrates disease relevant tissues.
Experimental Design. The distribution of 14C-Compound #10 were evaluated following a single oral gavage administration of 50 mg/kg (˜10 μCi/animal) of 14C-labeled Compound #10 to rats in a GLP study. For the quantitative whole-body autoradiography (QWBA) analysis, 1 animal/sex/timepoint was sacrificed at 6, 12, 24, 48, and 72 hours postdose as shown in Table 22.
a14C-Compound #10 was administered as a single-dose by oral gavage in L23 vehicle (35% Gelucire, 35% Labrafac, and 30% Solutol).
bFor 1 animal per sex at each timepoint, a blood sample was collected at the time of sacrifice for assessments of concentrations 14C-Compound #10 in blood, plasma, and tissues, and for calculation of tissue:plasma concentration ratios at the specified times postdose.
For the QWBA, the carcasses were prepared by immediately freezing them, embedding them in chilled carboxymethylcellulose, and freezing them into blocks. Appropriate cryomicrotome sections of the blocks at 40 μm thickness were collected on adhesive tape. Mounted sections were tightly wrapped and exposed on phosphorimaging screens along with plastic embedded autoradiographic standards. Exposed screens were scanned and the autoradiographic standard image data were sampled to create a calibrated standard curve. Specified tissues, organs, and fluids were analyzed. Tissue concentrations were interpolated from each standard curve as nanocuries per gram and then converted to μg equivalents/gram on the basis of the Compound #10 specific activity.
Results. All animals appeared healthy and exhibited no overt signs of toxicity throughout the study. In this study, absorbed radioactivity was rapidly distributed into the whole body with the Tmax in blood and plasma occurring at 4 hours postdose in both sexes. Excluding the gastrointestinal tract, Cmax values in most tissues occurred at 6 to 12 hours postdose, with the highest values occurring in lipomatous tissues such as adrenal gland, brown fat, and liver. By 72 hours postdose, discernable residual radioactivity remained concentrated in fatty tissues in both sexes.
As shown in Table 23, the tissue:plasma concentration ratios were greater than 1 in most tissues. At 72 hours postdose, the highest tissue:plasma concentration ratios were in fat with values ranging from 37.1 to 63.9 in both sexes. All other tissues had ratios less than 10 with the exception of female bone marrow, Harderian gland, ovary, and skin, which had values of 18.8, 12.0, 28.1, and 11.4, respectively. There were no remarkable gender related differences in absorption, distribution, and elimination of radioactivity.
This example demonstrates that Compound #10 penetrates disease relevant tissues.
9.3 Cell Cycle Delay
9.3.1 Cell Based Assays
This example demonstrates that a Compound induces a cell cycle delay at the G1/S-phase border.
Experimental Design. During in vitro evaluations of Compound #10 and Compound 1205 effects on VEGF expression, an examination of the effect on tumor cell cycling was performed. HT1080 cells were incubated under normoxic conditions (21% oxygen) for 18 hours with vehicle (0.5% DMSO) alone, or with a range of concentrations of Compound #10 from 0.3 nM to 100 nM, or 10 nM of Compound 1205. Compounds shown in Table 24 were incubated under normoxic conditions for 18 hours with vehicle or Compound #10 at a single dose of 100 nM. After treatment, cells were trypsinized, and stained with propidium iodide (PI) dye to measure DNA content of individual cells by flow cytometry. Output comprised histograms showing relative DNA content in 10,000 cells.
Results. As shown in
For additional Compounds shown in Table 24, the test results are expressed as the percentage of cells in the S-phase compared to a DMSO control (17.3% cells in S-Phase). While compounds which cause greater than 20% of the cells to accumulate in S-phase at 100 nM are considered active, a larger percentage of cells may be accumulated in S-phase at lower doses depending on the Compound, as shown in
This example demonstrates that the effect of Compound #10 on cell cycle delay is reversible.
Experimental Design. HT1080 cells were incubated under normoxic conditions (21% oxygen) for 14 hours with Compound #10 (100 nM) or with vehicle (0.5% DMSO) alone. Compound #10 was then washed out of the cultures and cells were harvested and analyzed by PI staining and flow cytometry (as described in Section 9.3.1.1) at 0, 2, 5, 8, and 26 hours after discontinuation of treatment.
Results. As shown in
This example demonstrates that Compound #10 cell cycle delay is coincident with the inhibition of VEGF production.
Experimental Design. Several VEGF secreting cell lines were assayed for cell cycle effects. Actively proliferating cells were incubated for 18 hours under normoxic conditions (21% oxygen) with vehicle (0.5% DMSO) alone or with Compound #10 at concentrations of 10 nM or 100 nM. At the completion of treatment, cells were harvested and cellular DNA content was analyzed via PI staining and flow cytometry (as described in Section 9.3.1.1).
Results. In the same cell lines, treatment was undertaken for 48 hours with a range of concentrations of Compound #10 from 0.1 nM to 30 μM or with vehicle (0.5% DMSO) alone. The conditioned media were collected and assayed by ELISA for soluble VEGF121 and VEGF165 isoforms (as described in Section 9.1.1.1); results were calculated as percentage inhibition relative to vehicle treated controls. EC50 values were calculated from the concentration response curves.
As shown in Table 25, Compound #10 cell cycle delay was coincident with the inhibition of VEGF production in all of the tested tumor types.
This example demonstrates the rate and number of cells transiting the S-phase of the cell cycle.
Experimental Design. HT 1080 cells are exposed to BrdU (bromodeoxyuridine, a synthetic nucleoside that is an analogue of thymidine and is incorporated into DNA during the S phase of cell division) (FITC BrdU Flow Kit, BD Pharmingen catalog #552598). Cells are grown and treated as described in Section 9.3.1.3 above with the exception that one hour prior to harvesting by trypsinization, BrdU (final concentration 1 μM) is added to each culture for 1 hour. Cells actively replicating DNA during this brief time incorporate the BrdU into the DNA, which can then be quantitated. BrdU content is quantitated with using the FITC BrdU Flow Kit as instructed by the manufacturer. The process includes fixation (paraformaldehyde) and DNA staining with 7-AAD (7-amino-actinomycin D) followed by incubation with a fluoro-tagged anti-BrdU antibody that specifically recognizes BrdU incorporated into DNA. Dual channel FACS analysis permits assessment of both the DNA content of individual cells and the rate of transit across the S-phase, which is assessed based upon BrdU incorporation over the one hour treatment period.
Results.
This example demonstrates the effect of a Compound provided herein on the 3-dimensional growth of HT1080 cells.
Experimental Design. HT1080 cells grown as a monolayer were trypsinized and seeded onto a 0.75% agar noble base to prevent the cells from attaching to the bottom of the tissue culture plate and to allow/promote the cells to self-adhere and grow as 3-dimensional spheroids. After 4 days the spheroids were established and the liquid growth medium was replaced with medium containing either 0.5% DMSO vehicle, or 10 nM or 50 nM of Compound #10 with 0.5% DMSO vehicle. The cells were incubated for 22 and 45 hours at 37° C., in the presence of a 10% CO2 atmosphere. Spheroids were visually checked daily for morphological changes and a medium was replenished two times per week. At 22 and 45 hours after exposure to Compound #10, BrdU was added to a subset of the wells designated for FACS analysis and then returned to the incubator for 3 hours to permit cells synthesizing DNA (i.e. cells in S-phase) to incorporate the BrdU into the nascent strands of DNA. These pulse labeled spheroids were then harvested, washed and trypsinized (triple action solution, Gibco), pelleted and prepared for FACS analysis with a FITC BrdU Flow Kit, (BD Pharmingen). Cells were fixed and permeabilized with paraformadehyde and DNA stained with 7-AAD followed by incubation with an antibody which specifically recognizes BrDV incorporated into DNA. As described in Section 9.3.1.4. Cells were analyzed and sorted by 7-AAD signal (DNA content) to determine cell cycle phase, and BrdU content (percent actively synthesizing DNA).
Results. HT1080 spheroids prepared as above were treated with a Compound provided herein for 24 (
Spheroids, prepared as above, were treated with either vehicle alone (0.5% DMSO v/v final) added to the media or a Compounds provided herein (10 nM or 50 nM final concentration) in media to which vehicle has been added. The cells were photographed on day 5 of treatment to assess any gross morphological differences caused by exposure to Compound #10. Spheroids from all treatment groups looked indistinguishable from one another (data not shown). In addition, spheroids maintained in the presence of Compound #10 provided herein for three weeks also display no obvious morphological changes (data not shown).
This example demonstrates that Compound #10 inhibits or reduces the ability of cells to migrate out of spheroids of HT1080 cells.
Experimental Design. To assess the viability and motility of HT 1080 cells exposed to Compound #10, spheroids of HT1080 cells were prepared as in Section 9.3.1.5. The cells were cultured in media with vehicle only (0.5% DMSO) or in the presence of 50 nM Compound #10 present in media with vehicle added. After three weeks of treatment, treated spheroids were re-plated into wells without an agar base, thus allowing cells to migrate out onto the coated surface and grow as a two-dimensional (2-D) monolayer in the presence or absence of Compound #10 at 50 nM. Pictures were then taken 48 hours to assess the migration and proliferation of the cells across the well's surface.
Results. Cells from vehicle treated spheroids plated out in the absence of Compound #10 migrate to cover the entire surface of the tissue culture plate within the 48 hours. Spheroids grown for 3 weeks in the presence of Compound #10 and re-plated in the absence of the compound also migrate out of the spheroid to cover the surface of the tissue culture plate within 48 hours. This indicates that a three-week exposure to Compound #10 does not reduce either the proliferative or the migratory capacity of HT1080 cells.
Cells from control spheroids grown in the absence of Compound #10 and subsequently re-plated in the presence of 50 nM of Compound #10 are blocked in their ability to migrate out of the spheroid, and do not cover the surface of the tissue culture plate. Similarly, cells grown as spheroids in tissue culture media containing 50 nM of Compound #10 herein and re-plated in the presence of Compound #10 migrate much less than other groups. The data suggests that, even after three weeks of growth in three dimensions (3-D), the cell cycle delay and migratory inhibition of Compound #10 herein are still intact once the cells move into 2-D culture. The data further suggests that Compound #10 can act to inhibit the metastasis of cells from tumors.
This example demonstrates that Compound #10 may reduce formation of colonies from HT1080 cells treated with Compound #10.
Experimental Design. HT1080 cells growing in monolayer were trypsinized, counted and suspended in a 0.35% agar noble/1× complete DMEM solution at 37° C. at a concentration of 2,500 cells/mL. One ml of this solution was layered over a semisolid base consisting of 0.5 mL of 0.75% agar noble/1× complete DMEM in a six well tissue culture plate. The top layer was permitted to solidify at room temperature, whereupon 1.5 mL of liquid medium (complete DMEM) containing 0.5% DMSO and 0, 5, 20 or 100 nM of Compound #10 was added to achieve a final concentration of 0, 2.5, 10 or 50 nM of Compound #10. Tissue culture plates were then returned to the incubator and colonies were allowed to form. The top medium layer was replaced periodically (every 3-4 days) with complete DMEM containing either 0.5% DMSO or Compound #10 (0, 2.5, 10 or 50 nm) and 0.5% DMSO. On day 18 the vehicle-treated wells had colonies of sufficient size to count (>50 cells/colony). At this time, for increased visualization, 1.5 mL of a 2× working volume of (3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide, a tetrazole) (MTT, Invitrogen, Cat #C35007) was added and the plates were returned to the incubator for 2 hours until colonies were stained by conversion of the MTT to purple formazan crystals. Colonies were then visually counted under a dissecting microscope.
Results.
9.3.2 Animal Model Systems
This example demonstrates that Compound #10 induces a S-phase cell delay in dividing tumor cells in vivo.
Experimental Design. HT1080 cells (5×106 cells/mouse) were implanted subcutaneously in male athymic nude mice. When tumors had become established (i.e., the mean tumor size had reached 585±150 mm3), mice were divided into 4 treatment groups, as shown in Table 26. Positive and negative controls for effects on tumor cell cycling included doxorubicin and bevacizumab, respectively.
After 1, 2, or 3 days of treatment with Compound #10, mice were injected with BrdU, a synthetic nucleoside that is an analogue of thymidine and is incorporated into DNA during the S phase of cell division. The mice were sacrificed 3 hours later, and the tumors collected. A single cell suspension was prepared from the tumor cells. The cells were permeabilized and an antibody to BrdU was used to stain cells that had entered S phase during the labeling period. The proportion of cells actively synthesizing DNA was determined by cell sorting.
aTreatments were initiated on Day 0 with 20 mice per group. On each day, 5 mice were sacrificed per group for analysis. Mice were treated with Compound #10 daily. Mice were treated with doxorubicin or bevacizumab on Day 0 only.
bVehicle was L21 (35% Labrasol, 35% Labrafac, and 30% Solutol).
As shown in
When taken together with reductions in tumor derived plasma VEGF in these same animals (Section 9.2.3), these results are consistent with the previous in vitro results for Compound #10, suggesting that Compound #10 selectively induces a S phase cell delay in rapidly dividing tumor cells.
10.1 Pre-Clinical Studies
In vitro and in vivo safety pharmacology studies with Compound #10 demonstrate a favorable safety profile. Based on the safety pharmacology studies and results of electrocardiograms (ECGs) and blood pressures collected during 7- and 28-day toxicity studies in dogs, Compound #10 is unlikely to cause serious adverse effects on the central nervous, cardiovascular, and respiratory systems.
A functional observation battery in Sprague Dawley rats dosed daily for 7-days by oral gavage at dose levels of 40, 120, and 400 mg/kg revealed no adverse behavioral or neurological effects at any dose level.
Compound #10 was considered negative for meaningful inhibition of human-ether-a-go-go-related gene (hERG) current in a higher throughput hERG assay. In a cardiovascular safety pharmacology study in awake telemeterized male beagle dogs, single oral doses of 30, 60, and 120 mg/kg of Compound #10 induced no meaningful changes in cardiovascular or electrocardiographic (including QT interval) parameters. In addition, ECG analysis and blood pressure assessments were performed as part of 2 GLP toxicity and toxicokinetic studies of Compound #10 in beagle dogs, one with 7-days of dosing and one with 28-days of dosing followed by a 15-day recovery period. In these studies, oral dosing with Compound #10 at dose levels through 120 mg/kg/day for 7-days and through 60 mg/kg/day for 28-days did not have any toxicological effects on ECG or blood pressure results in dogs. At the end of dosing in the 28-day toxicity study in dogs, males in the 60 mg/kg/day group had a slightly higher (7%) mean uncorrected QT value which also was statistically significant in comparison to controls. However, QTc (QT interval corrected for heart rate) values in males in the 60 mg/kg/day group were comparable to controls.
In a respiratory safety pharmacology study in awake telemeterized male beagle dogs, single oral doses of 30, 60, and 120 mg/kg of Compound #10 induced no dose dependent or biologically significant changes in respiratory rate, core body temperature, arterial blood gases, arterial pH, or arterial bicarbonate.
The absorption of Compound #10 was evaluated in nude mice, C57BL/6 mice, Sprague Dawley rats, and beagle dogs dosed by the oral route. The pharmacokinetic evaluations in mice were adjuncts to the primary pharmacodynamic xenograft studies. The evaluations in rats included toxicokinetic assessments in single-dose, 7-day, and 28-day toxicology studies as well as a mass-balance study after a single oral dose of 14C-Compound #10. The evaluations in dogs included toxicokinetic assessments in 7-day and 28-day toxicology studies. In the studies performed, rodents were dosed once daily with Compound #10 formulated in vehicle and administered via oral gavage. Dogs were dosed BID at ˜12-hour intervals between doses with Compound #10 formulated in vehicle and loaded into gelatin capsules that were administered orally.
The results of the PK studies demonstrate that Compound #10 is orally bioavailable in mice, rats, and dogs. Compound #10 pharmacokinetic parameters have been evaluated in mice at the 1-mg/kg dose level that, when given BID, was associated with maximal antitumor activity in the HT1080 human tumor xenograft model. At Day 1, Compound #10 plasma trough concentration of ˜0.10 to 0.15 μg/mL at 24 hours was established as the minimal mean target plasma concentration to be achieved in pharmacokinetic studies.
In all mice, rats, and dogs, the relationship between Compound #10 dose and plasma exposure describes a “bell-shaped curve,” i.e., plasma exposures initially rise with dose but then decrease despite further increases in dose. These bell-shaped dose-exposure relationships are consistent with absorption saturation and/or possible precipitation of the Compound within the gastrointestinal tract at the highest dose levels. The dose exposure curves were used in the dose selection for the rat and dog toxicology studies and in the interpretation of the No-Observed-Adverse-Effect Levels (NOAELs) from these studies. In both rat and dog toxicology species, Cmax and AUC values at the NOAELs exceed those expected in subjects to be enrolled to the proposed Phase 1b clinical study in patients with advanced breast cancer.
In vitro plasma protein binding for 14C-radiolabeled Compound #10 was determined from plasma samples obtained from mice, rats, dogs, monkeys, and humans. 14C-radiolabeled Compound #10 was highly bound to proteins in the plasma in vitro, with an overall mean of ≧99.5% for all species. Protein binding was independent of concentration over the range of 0.05 to 50 μg/mL of 14C-radiolabeled Compound #10. Given the similarities in protein binding across species, these data suggest that cross-species exposure comparisons do not need to be adjusted to take protein binding into account.
When evaluated in human hepatic microsomes or in assays using human recombinant cytochrome P450 (CYP) isoenzymes, Compound #10 inhibits the activity of the CYP2D6 isoenzyme. No meaningful inhibition of CYP3A4, CYP1A2, CYP2C9, or CYPC19 was observed. These data suggest the possibility that Compound #10 may slow or alter the clearance of drugs that are primarily metabolized by CYP2D6. It is possible that in certain clinical trial subjects, such agents may need to be adjusted for dosing or replaced by alternative agents that are not metabolized by CYP2D6, particularly when such agents may have a low therapeutic index.
10.1.2 Toxicology
A comprehensive toxicology program has been completed for Compound #10, consisting of a single-dose oral study in rats, 7-day oral studies in rats and dogs, and 28-day oral studies in rats and dogs each with a 2-week recovery period. A battery of genotoxicity studies was also performed. For the toxicology studies conducted in vivo, the study design consisted of a vehicle control group and 3 dose levels of Compound #10. The L23 vehicle was used. In rats, the vehicle or Compound #10 formulated in vehicle was administered by oral gavage. In dogs, the vehicle alone or Compound #10 formulated in vehicle was loaded into gelatin capsules for oral administration of 2 equal doses ˜12 hours apart (BID). All studies in the toxicology program were conducted according to GLP regulations.
In rats given single oral gavage doses of Compound #10 at doses of 100, 200, or 400 mg/kg, no notable clinical or clinical pathological toxicities were observed at any dose level. Because maximal exposure occurred at 100 mg/kg, this dose is considered the NOAEL for 1 day of dosing.
In the subsequent 7-day study, rats administered oral gavage Compound #10 doses of 40, 120, and 400 mg/kg/day. Maximal exposures occurred at a dose of 120 mg/kg/day. At this dose, notable changes included increases in mean prothrombin time (PT) and mean activated partial thromboplastin time (aPTT) in males but not in females. Elevations of about ˜2.5-fold to about 3-fold in mean cholesterol levels and about 1.3-fold in mean glucose levels were also noted in males and females receiving Compound #10. Based on the collective toxicity and toxicokinetic findings, the NOAEL for 7-days of Compound #10 administration for male rats is 40 mg/kg/day and for female rats is 120 mg/kg/day.
In the 28-day study (with a 14-day recovery period), rats received oral gavage Compound #10 doses of 12, 40, and 120 mg/kg/day. Exposures were maximal at 120 mg/kg/day. Consistent with the 7-day study, the 28-day study showed reversible increases in mean PT and aPTT at Compound #10 doses of 40 and 120 mg/kg/day in males but not in females. Other chemistry changes included about 2- to about 3-fold elevations in mean cholesterol levels in all Compound #10 dose groups, and minimally increased glucose and alkaline phosphatase values in females and minimally increased chloride and minimally decreased potassium values in males dosed with Compound #10 at 40 and 120 mg/kg/day. Increased adrenal weights were observed at all dose levels; these changes correlated with adrenal cortical hypertrophy that was observed in males and females. The findings indicate an NOAEL for 28-days of Compound #10 administration in rats of 12 mg/kg/day.
In dogs given Compound #10 at doses of 10, 30, or 60 mg/kg/dose BID (20, 60, and 120 mg/kg/day) orally in L23 gelatin capsules for 7 consecutive days, exposures were maximal at 30 mg/kg/dose BID. Animals receiving Compound #10 had an increased incidence and frequency of soft stools in both males and females but no other notable treatment-related drug-related effects. Considering exposure values, the NOAEL for 7-days is considered to be 30 mg/kg/dose BID (60 mg/kg/day).
In the 28-day study (with a 15-day recovery period), dogs were administered Compound #10 doses of 5, 15, and 30 mg/kg/dose BID (10, 30, or 60 mg/kg/day) in gelatin capsules. Maximal exposures occurred at 30 mg/kg/dose BID (60 mg/kg/day). Compound #10 was clinically well tolerated in male and female dogs at the low- and mid-dose levels but at the high dose, adverse clinical findings, and decreased food consumption resulting in decreased body weights were observed. The target organ of toxicity was the small intestine. Microscopic findings of erosion, necrosis and/or ulceration of the mucosa, submucosal inflammation, epithelial hyperplasia of the mucosa of the crypts, and/or congestion of the Peyer's patches in the small intestine were seen in several dogs at the high dose. The findings in the small intestine did not reverse at the end of the 15-day recovery period. Based on the findings, the NOAEL for 28-days of Compound #10 administration in dogs is considered to be 15 mg/kg/dose BID (30 mg/kg/day).
Genotoxicity was assessed in a battery of in vitro and in vivo studies that included a bacterial reverse mutation study, a chromosome aberration study in Chinese hamster ovary (CHO) cells, and a micronucleus study in rats by the oral route. The in vitro studies were performed in the presence and absence of an exogenous metabolic activation system. There was no evidence of genotoxic effects with Compound #10 in these studies.
10.2 Clinical Studies:
Compound #10 has been evaluated in a Phase 1, escalating multiple-dose, safety, tolerability and pharmacokinetic (PK) study in healthy adult volunteers.
The study was performed under the oversight of the French health authorities. The study was not performed under an IND. The primary objective of the study was to determine a dose range and regimen for Compound #10 that safely achieves and maintains pharmacologically active target plasma concentrations (as determined from xenograft studies) and would be appropriate for use in subsequent Phase 1 or Phase 2 studies in patients with cancer. The secondary objective was to evaluate the safety profile of multiple doses of Compound #10 administered 2 times per day (BID) (Stage 1) or 3 times per day (TID) (Stage 2) in oral capsules, to characterize the multiple dose PK profile of Compound #10, and to assess the effect of Compound #10 on plasma and serum physiological VEGF concentrations.
Methods. The trial was a Phase 1, randomized, escalating multiple dose, single center study conducted in 2 stages. Stage 1 comprised a double blind, placebo controlled dose escalation with Compound #10 given BID. Stage 2 comprised a double blind, placebo controlled escalation of Compound #10 given TID. The number of subjects planned and enrolled for stage 1: 24 subjects as 3 cohorts of 8 subjects, with each cohort comprising 4 males (3 Compound #10, 1 placebo) and 4 females (3 Compound #10, 1 placebo). The number of subjects planned and enrolled for stage 2: 1 cohort of 8 subjects comprising 4 males (3 Compound #10, 1 placebo) and 4 females (3 Compound #10, 1 placebo).
Diagnosis and Main Criteria for Inclusion: Subjects were required to be healthy males or females, 18 to 65 years old, weighing 41 to 90 kg. Female subjects were required to be surgically sterile or post menopausal (as documented by an absence of menses for >1 year before screening).
Test and Reference Products: In Stage 1, Compound #10 was provided in gelatin capsules for oral administration. Capsules contained 2 mg or 20 mg of active substance. Cohorts of subjects assigned to active treatment received progressively higher Compound #10 doses of 0.3, 0.6, and 1.2 mg/kg BID (0.6, 1.2, and 2.4 mg/kg/day).
In Stage 2, Compound #10 was provided in gelatin capsules for oral administration. Capsules contained 20 mg or 25 mg of active substance. The cohort of subjects assigned to active treatment received a Compound #10 dose of 1.6 mg/kg TID (4.8 mg/kg/day).
Placebo gelatin capsules for oral administration were used as the reference product in both Stage 1 and Stage 2 of the study.
Duration of Treatment: Stage 1: Compound #10 or placebo was administered orally BID for 7 days (Day 1 through Day 7). Stage 2: Compound #10 or placebo was administered orally TID for 7 days (Day 1 through Day 7).
Criteria for Evaluation: Maximum tolerated dose; Safety as characterized by type, frequency, severity, timing, and relationship to study treatment of any adverse events, laboratory abnormalities, or electrocardiogram (ECG) abnormalities; PK profile of Compound #10 as described by plasma concentration time curves and by derived PK parameters; Plasma and serum VEGF concentrations.
Statistical Methods: The results were summarized by study stage, treatment, and dose.
Pharmacokinetics: Compound #10 concentrations and PK parameters were presented descriptively. Noncompartmental methods were used to compute Tmax, Cmax, and AUC. Dose proportionality and sex effect were evaluated using ANOVA on log transformed PK parameters using dose, sex, and dose by sex as fixed factors.
Plasma VEGF Concentrations: Plasma and serum VEGF concentrations and concentration changes from baseline were presented descriptively.
Results. As planned, 32 subjects were included in the study. In Stage 1, 8 subjects were enrolled to each of the 3 dose groups (3 males and 3 females receiving Compound #10 and 1 male and 1 female receiving placebo) resulting in enrollment of 24 subjects (12 males and 12 females). In Stage 2, 8 subjects (3 males and 3 females receiving Compound #10 and 1 male and 1 female receiving placebo) completed their participation in the study. No subject discontinued prematurely and all subjects completed the study. Subject characteristics for Stage 1 and Stage 2 are described in Table 27 below. Demographic characteristics in Stage 1 were generally similar between the Compound #10 and placebo groups. Characteristics in Stage 2 were generally similar to those in Stage 1.
Pharmacokinetics: Mean plasma concentration time profiles for Compound #10 are shown in
PK parameters for Compound #10 in plasma are shown in Table 28 below. The mean Tmax was in the range of ˜3 hours. During Stage 1 and Stage 2, increases in mean values for Cmax and area under the concentration time curve over 24 hours (AUC0-24) were generally dose proportional. When comparing Day 1 to Day 7, there was an increase in the mean Cmax and AUC0-24 over time at all dose levels, indicating accumulation (˜2-fold) when Compound #10 was dosed continuously. A 2-compartment model could be readily fit to all of the individual subject data throughout the 7 day course of treatment.
Gender related differences were analyzed by ANOVA. In this study, no significant differences in Cmax or AUC0-24 values were observed between males and females.
Circulating VEGF Concentrations: Plasma and serum VEGF A concentrations were assayed in all subjects. Mean absolute values and changes from baseline in plasma and serum VEGF A concentrations are plotted in
Results: In this Phase 1 dose study of Compound #10 in healthy volunteer males and females, administration of Compound #10 for 7 consecutive days at doses of 0.3, 0.6, and 1.2 mg/kg BID (0.6, 1.2, and 2.4 mg/kg/day) and at 1.6 mg/kg TID (4.8 mg/kg/day) was well tolerated. Treatment emergent adverse events and laboratory abnormalities were generally Grade 1. The incidence or severity of these findings was not clearly greater in the Compound #10 group than in the placebo group and no dose dependency was apparent. Frequent ECG evaluations revealed no concerning rhythm, waveform, or interval changes. In particular, no meaningful QTc prolongation was observed. No serious adverse events or premature discontinuations due to adverse events occurred. Interventions for adverse events were minimal. None of the safety findings were deemed clinically significant by the investigator. No MTD was established and no dose limiting toxicities were observed through the highest dose level tested (1.6 mg/kg TID).
PK data indicated that Compound #10 is orally bioavailable. The mean Tmax was in the range of ˜3 hours. Increases in Cmax and AUC were generally proportional with dose. There was ˜2 fold accumulation when Compound #10 was dosed continuously. In this study, no significant differences in Cmax or AUC0-24 values were observed between males and females. Target trough plasma concentrations of ≧100 to 150 ng/mL derived from preclinical human tumor xenograft models were achieved and maintained at all dose levels in the current study.
No significant alterations in plasma or serum physiological VEGF-A concentrations were observed at any of the Compound #10 doses tested in this multiple dose study. The finding that Compound #10 did not affect physiological plasma or serum VEGF levels in healthy volunteers appears consistent with in vitro results suggesting that Compound #10 does not perturb physiological VEGF production, but acts selectively to inhibit pathological VEGF production (induced by hypoxia or tumor transformation). Lack of changes in circulating VEGF concentrations may correlate with the lack of Compound #10 toxicities (e.g., hypertension, bleeding, proteinuria) in this trial. Such toxicities have been classically associated with currently used drugs that inhibit VEGF signaling at endothelial cells.
Collectively, the safety and PK findings of this study in healthy volunteers indicate that the dosing regimens tested in this study can readily attain target trough plasma concentrations known to be active in nonclinical models of human disease and that oral BID administration of Compound #10 may offer safety and ease of use advantages over existing clinical methods of inhibiting VEGF signaling.
Subjects with metastatic breast cancer may receive continuous oral administration of 0.3 mg/kg/dose (approximately 20 mg/dose), 0.6 mg/kg/dose (approximately 40 mg/dose), or 1.2 mg/kg/dose (approximately 80 mg/dose) of a Compound two times a day (BID) for 4 weeks in repeated 6-week cycles until disease progression, or as appropriate. Subjects with metastatic breast cancer may receive continuous administration of 100 mg/dose of a Compound BID for 4 weeks in repeated 6-week cycles in combination with continuous oral administration of 1 mg/dose of Anastrozole (Arimidex®) once per day (QD), 2.5 mg/dose of Letrozole (Femara®) QD, or 25 mg/dose of Exemestane (Aromasin®) QD until disease progression, or as appropriate. In a specific embodiment, the Compound is Compound #10 or Compound #1205.
Clinical Objectives: Clinical objectives include:
Clinical Endpoints: Clinical endpoints for efficacy of a Compound for treating metastatic breast cancer include one or more of the following: (1) a reduction in the circulating concentrations of VEGF relative to pretreatment baseline circulating concentrations of VEGF; (2) antiangiogenic or anti-inflammatory activity as documented by changes in circulating concentrations of either angiogenic mediators other than VEGF (e.g., VEGF165b, VEGFR, VEGF-C, VEGF-D, P1GF), inflammatory cytokines (e.g., IL-6, IL-8) or both relative to pretreatment baseline circulating concentrations of angiogenic mediators and inflammatory cytokines; (3) a reduction in tumor perfusion as assessed by DCE-MRI; (4) a change in tumor metabolism as assessed by changes in 18F-2-fluorodeoxyglucose positron emission tomography (FDG-PET) standardized uptake value (SUV) in a target tumor lesion; (5) a reduction in tumor size relative to pretreatment tumor size; (6) an increase in progression-free survival (PFS); and (7) a reduction in tumor markers relative to pretreatment baseline tumor markers. Other clinical endpoints include: (1) determining the MTD of a Compound within the tested dose range; (2) determining the feasibility of a Compound combination therapy with oral hormonal agents used in breast cancer therapy; (3) determining the overall safety profile of a Compound alone and in combination with hormonal agents characterized in terms of the type, frequency, severity, timing, and relationship to study therapy of any adverse events or abnormalities of physical findings, laboratory tests, or ECGs, and the occurrence of any DLTs (Dose Limiting Toxicities), Compound treatment discontinuations due to adverse events, or serious adverse events; and (4) determining PK parameters (e.g., Tmax, T1/2, Cmax, Ctrough, AUC).
Evaluation of Clinical Endpoints
Antitumor activity: Accepted clinical, radiographic, and tumor marker response criteria can be used to evaluate the ability of the treatments to specifically induce tumor shrinkage and/or maintain tumor control. The RECIST method (Therasse et al., 2000, New guidelines to evaluate the response to treatment in solid tumors. European Organization for Research and Treatment of Cancer, National Cancer Institute of the United States, National Cancer Institute of Canada. J Natl Cancer Inst. 92(3):205-16; Therasse et al., 2006, RECIST revisited: a review of validation studies on tumor assessment. Eur J Cancer., 42(8):1031-9) wmay be employed to simplify tumor lesion measurement. Commonly employed tumor markers (carcinoembryonic antigen [CEA] and cancer antigen 27.29 [CA 27.29]) can be assessed (Bast et al., 2001, American Society of Clinical Oncology Tumor Markers Expert Panel. 2000 update of recommendations for the use of tumor markers in breast and colorectal cancer: clinical practice guidelines of the American Society of Clinical Oncology. J Clin Oncol., 19(6):1865-78; Erratum in: J Clin Oncol 2001 Nov. 1; 19(21):4185-8. J Clin Oncol 2002 Apr. 15; 20(8):2213).
Tumor perfusion using DCE-MRI: Assessing tumor blood flow offers an additional parameter of Compound action that can confirm the downstream consequences of decreasing tumor VEGF. Measurement of blood flow in target lesions provides direct evidence of Compound action on tumors that can be correlated with plasma VEGF changes. Assessment of tumor perfusion using DCE-MRI may be used to evaluate the efficacy of a Compound using standard protocols (see., e.g., Morgan et al., J. Clin. Oncol., Nov. 1, 2003, 21(21):3955-64; Leach et al., Br. J. Cancer, May 9, 2005, 92(9):1599-610; Liu et al., J. Clin. Oncol., August 2005, 23(24): 5464-73; and Thomas et al., J. Clin. Oncol., Jun. 20, 2005, 23(18):4162-71).
Anti-angiogenic activity: Assessing circulating VEGF concentrations provides a relevant and convenient mechanism-specific marker of Compound activity. Appropriate methods for the measurement of circulating VEGF concentrations have been determined (see, e.g., Jelkmann et al., Clin. Chem., April 2001, 47(4):617-23.), and such methods may be used to evaluate the effects of a Compound. For example, clinically validated ELISA kits (e.g., from R&D Systems, Minneapolis, Minn.) may be used to measure circulating concentrations of VEGF, VEGF-C, P1GF, VEGFR, and inflammatory mediators.
Safety: Adverse events that may be encountered in patients receiving a Compound may monitored. For consistency of interpretation, adverse events may be coded using the standard Medical Dictionary for Regulatory Activities (MedDRA), and the severity of these events may be graded using the well-defined Common Terminology Criteria for Adverse Events (CTCAE) Version 3.0. Standard definitions for seriousness may be applied.
Subject Selection
The following eligibility criteria may be used to select subjects for whom treatment with a Compound is considered appropriate. All relevant medical and non-medical conditions are taken into consideration when deciding whether this treatment protocol is suitable for a particular subject.
Subjects should meet the following conditions to be eligible for the treatment regimens (i.e., Treatment Regimen 1 & Treatment Regimen 2):
In addition to the criteria noted above, subjects should meet the following to be eligible for the treatment regimen involving the administration of 100 mg/dose BID of a Compound in combination with anastrozole, letrozole or exemestane (Treatment Regimen 2):
The presence of any of the following conditions may be contraindicated for the treatment of breast cancer with a Compound:
Compound Administration: Treatment Regimen #1
A Compound can be orally administered on an intermittent, cyclical basis. Each cycle may include administration of 56 doses of a Compound during a 4-week (28-day) period followed by a ≧2-week (14-day) washout period. Thus, a cycle in treatment regimen #1 can be defined as the period elapsing from the first day of Compound administration to Day 42 of the cycle or to the recovery from any adverse events sufficient that a new cycle can be administered (e.g., on Day 49 or Day 56), whichever occurs later. Once a new cycle is initiated, the prior cycle is considered to be completed.
A Compound can be orally administered as a single-agent each day for the first 28 consecutive days of each cycle. The Compound can be administered on a BID schedule at approximately the same times each day. Ideally doses should be taken at ˜12-hour intervals (e.g., at ˜7:00 AM and at ˜7:00 PM). If convenient for the subject, the Compound may be taken during or within ˜30 minutes after a meal; however, administration with food is not required. Subjects may continue receiving repeated cycles of a Compound indefinitely or until termination. Compound administration may be terminated because of, e.g., tumor progression or a dose-limiting toxicity.
Each subject can be assigned sequentially to a dosage group—Dosage Group 1 (0.3 mg/kg/dose BID), Dosage Group 2 (0.6 mg/kg/dose BID), or Dosage Group 3 (1.2 mg/kg/dose BID). If no dose-limiting toxicity (DLT) is experienced by subjects assigned to a particular dosage group during the first 6 week cycle, then other subject may be assigned to the next higher level of dosage groups. For example, if no DLT is experienced by subjects in Dosage Group 1 (i.e., subjects receiving a dosage of 0.3 mg/kg/dose BID) during the first 6 week cycle, then subsequent subjects may be assigned to Dosage Group 2 and administered a dose of 0.6 mg/kg/dose BID. If a DLT is experienced by a subject in a dosage group, then subsequent subjects will be assigned to the same dosage group. No dose escalation will occur unless none of the additional subjects experience a DLT. If any of the additional subjects experience a DLT, then the MTD may have been exceeded and subsequent subjects will be assigned to the next lower dosage group. For example, if a DLT is experienced by 1 of 3 subjects assigned to Dosage Group 1, then 3 more additional subjects will be assigned to the same dosage group (i.e., Dosage Group 1). If any one of these additional subjects experiences a DLT, then the MTD may have been exceeded and subsequent subjects will be to the next lower dosage group, e.g., Dosage Group 4 (0.1 mg/kg/dose BID).
The occurrence of DLT during the first cycle in treatment regimen 1 can be used to define the MTD. DLT may be defined as the occurrence of any of the following:
Toxicities can be graded according to the CTCAE, Version 3.0. If multiple toxicities are seen, the presence of DLT may be based on the most severe toxicity experienced.
Treatment Regimen #2: A Compound may be administered on a cyclical basis, wherein a cycle may be defined as the period elapsing from Day 1 of the cycle through Day 42 of the cycle or to the recovery from any adverse events sufficient that a new cycle can be administered (e.g., on Day 50 or Day 57), whichever occurs later. Once a new cycle is initiated, the prior cycle is considered to be completed.
A Compound may be given orally each day continuously starting on Day 1 of each cycle. A Compound may be administered on a BID schedule at approximately the same times each day; therefore 84 planned doses of a Compound may be delivered during the 6-week (42-day) period in each cycle. Ideally, Compound doses should be taken at ˜12-hour intervals (e.g., at ˜7:00 AM and at ˜7:00 PM). If convenient for the subject, the Compound may be taken during or within ˜30 minutes after a meal; however, administration with food is not required. Subjects may continue receiving repeated cycles of a Compound indefinitely or until termination. Compound administration may be terminated because of, e.g., tumor progression or a dose-limiting toxicity.
The dosage of a Compound administered to a subject may be successively reduced from 100 mg/dose BID to 80 mg/dose BID to 60 mg/dose BID if a Compound-related DLT occurs. DLT may be defined as the occurrence of any of the following:
Toxicities may be graded according to the CTCAE, Version 3.0. If multiple toxicities are seen, the presence of DLT will be based on the most severe toxicity experienced.
Hormonal Therapy for Breast Cancer: Subjects can continue to receive already-prescribed hormonal therapy consistent with the instructions in the package insert. For subjects who are not already receiving hormonal therapy or are changing hormonal therapy, treatment with a new hormonal agent may begin concurrent with the initiation of Compound treatment.
Hormonal agents can be given orally each continuously. Recommended doses for the hormonal agents are:
1. Anastrozole (Arimidex®), 1 mg/dose QD, orally without regard to meals;
2. Letrozole (Femara®), 2.5 mg/dose QD, orally without regard to meals; and
3. Exemestane (Aromasin®), 25 mg/dose QD, orally after breakfast.
Because all of these drugs are given once per day, 42 doses of the hormonal therapy can be delivered during each 6-week (42-day) period in each Compound cycle. Ideally, hormonal therapy doses should be taken at ˜24-hour intervals (e.g., at ˜7:00 AM every day) concurrent with the morning dose of a Compound. If convenient for the subject, the drug may be taken during or within ˜30 minutes after a meal. Administration of anastrozole or letrozole with food is not required. Administration of exemestane with food is recommended.
LH-RH Agonists for Suppression of Ovarian Function: Subjects taking an LH-RH agonist (e.g., goserelin acetate [Zoladex®]), leuprolide acetate [Lupron®]), triptorelin pamoate [Trelstar®]) may continue to receive an already-prescribed drug consistent with the instructions in the package insert. For subjects who are not already receiving an LH-RH agonist and require such a drug to achieve suppression of ovarian function to post-menopausal status, treatment with such a drug may begin concurrent with the initiation of Compound treatment.
Subjects requiring LH-RH suppression of ovarian function may receive the LHRH agonist by subcutaneous injection at 1-, 3-, or 12-month intervals to maintain ovarian suppression, with the dose and dosing interval depending upon the type and formulation of the relevant drug. Use of a form of one of these drugs, that is appropriate for 3-month (12-week) intervals is recommended.
Schedule of Events and Procedures
Blood VEGF: Subjects can have a blood sample obtained for assessment of plasma and serum VEGF prior to initial administration of a Compound, and at other times as clinically relevant.
The sample for plasma collection may comprise 4 mL of venous blood drawn into a Vacutainer® tube with K2EDTA as the anticoagulant. Immediately after collection, the tube can be gently inverted 8 to 10 times to mix the anticoagulant with the blood sample. The tube can be stored upright at room temperature until centrifugation; centrifugation and sample processing should be performed within 30 minutes of sample collection. The plasma fraction can be separated by placing the collection tube into a room-temperature (18 to 25° C.) horizontal rotor (with a swing-out head) for 15 minutes at 1000 to 2500 RCF. Immediately following the completion of centrifugation, the plasma fraction can be withdrawn by pipette and divided into 2 polypropylene freezing tubes (with each tube receiving approximately equal aliquots).
Each sample for serum collection may comprise 5 mL of venous blood drawn into a Vacutainer® SS™ Tube. After collection, the tube can be stored upright at room temperature for 30 minutes to allow the sample to clot prior to centrifugation. The serum fraction can be separated by placing the collection tube into a room-temperature (18 to 25° C.), horizontal rotor (with a swing-out head) for 15 minutes at 1000 to 2500 RCF. Immediately following the completion of centrifugation, the serum fraction can be withdrawn by pipette and divided into 2 polypropylene freezing tubes (with each tube receiving approximately equal aliquots).
After processing, the sample may be placed into a freezer at approximately −70° C. until shipped to the analytical facility. Repeated freeze-thaw cycles should be avoided. A clinically validated ELISA kit will be used to measure plasma VEGF level.
β-Human Chorionic Gonadotropin: Women of childbearing potential may have serum beta human chorionic gonadotropin (βHCG) testing prior to initial administration of a Compound.
Estradiol and FSH: Premenopausal women who are scheduled to receive combination therapy of a Compound with an aromatase inhibitor (i.e., Treatment Regimen 2) may have serum estradiol and FSH tested prior to initial administration of a Compound.
Vital Signs: Vital signs (pulse and blood pressure) may be monitored prior to initial administration of a Compound, and at other times as clinically indicated.
Height, Body Weight, and Performance Status: Height (in cm) can be measured once prior to initial administration of a Compound. Body weight and ECOG performance status can be assessed prior to initial administration of a Compound, and at other times as clinically indicated.
Physical Examination: A physical examination can be conducted prior to initial administration of a Compound, and at other times as clinically indicated.
Hematology Laboratory Assessment: Hematology laboratory assessments can include white blood cell count with differential, hemoglobin, hematocrit, other red cell parameters, and platelet count. These parameters can be monitored prior to initial administration of a Compound, and at other times as clinically indicated.
Biochemistry Laboratory Assessment: Biochemistry laboratory assessments can include sodium, potassium, chloride, bicarbonate, blood urea nitrogen, creatinine, calcium, phosphorus, uric acid, glucose, total protein, albumin, globulin, albumin:globulin ratio, bilirubin (direct and indirect), aspartate aminotransferase, alanine aminotransferase, gamma glutamyl transferase, alkaline phosphatase, lactate dehydrogenase, total cholesterol, triglycerides, low-density lipoprotein, and high-density lipoprotein. These parameters can be monitored prior to initial administration of a Compound, and at other times as clinically indicated.
Coagulation Laboratory Assessment: Coagulation laboratory assessments can include PT and aPTT. These parameters can be prior to initial administration of a Compound, and at other times as clinically indicated.
Serum ACTH, Cortisol, and Aldosterone: Plasma for assessment of ACTH and serum for assessment of cortisol and aldosterone can be collected prior to initial administration of a Compound, and at other times as clinically indicated.
Urinalysis: Urinalyses include dipstick analysis for pH, specific gravity, glucose, ketones, blood, protein, urobilinogen, bilirubin, and microscopic examination. These parameters can be monitored prior to initial administration of a Compound, and at other times as clinically indicated.
12-Lead ECG: A 12-lead ECG can be obtained prior to initial administration of a Compound, and at other times as clinically indicated.
Blood for Pharmacokinetics: Blood for PK assessments can be collected prior to initial administration of a Compound, and at other times as clinically relevant.
Each sample may comprise 3 mL of venous blood drawn into a 5-mL Vacutainer® tube with K2 EDTA as the anticoagulant. Immediately after collection, the tube can be gently inverted 8 to 10 times to mix the anticoagulant with the blood sample. The tube can be stored upright on ice until centrifugation; centrifugation and sample processing can be performed within 1 hour of sample collection. The plasma fraction can be separated by placing the collection tube into a refrigerated centrifuge (4 to 8° C.) in a horizontal rotor (with a swing-out head) for a minimum of 15 minutes at 1500 to 1800 relative centrifugal force (RCF). The plasma fraction can be withdrawn by pipette and divided into 2 polypropylene freezing tubes (with each tube receiving approximately equal aliquots). After processing, samples can be placed into a freezer at approximately −70° C.
Analyses of the PK samples for a Compound can be performed using a validated LC-MS/MS method. Plasma samples collected for PK analysis can be preserved for potential future Compound metabolite and aromatase inhibitor concentration analyses, as appropriate.
Blood for Circulating VEGF and Angiogenic Cytokines: Two blood samples (1 for plasma and 1 for serum) can be obtained for assessment of circulating VEGF, VEGFR, and cytokine levels prior to initial administration of a Compound, and at other time as clinically relevant.
Each sample for plasma collection may comprise 4 mL of venous blood drawn into a Vacutainer® tube with K2EDTA as the anticoagulant. Immediately after collection, the tube can be gently inverted 8 to 10 times to mix the anticoagulant with the blood sample. The tube can be stored upright at room temperature until centrifugation; centrifugation and sample processing can be performed within 30 minutes of sample collection. The plasma fraction can be separated by placing the collection tube into a room-temperature (18 to 25° C.) horizontal rotor (with a swing-out head) for 15 minutes at 1000 to 2500 RCF. Immediately following the completion of centrifugation, the plasma fraction can be withdrawn by pipette and divided into 2 polypropylene freezing tubes (with each tube receiving approximately equal aliquots).
Each sample for serum collection may comprise 5 mL of venous blood drawn into a Vacutainer® SST™ Tube. After collection, the tube can be stored upright at room temperature for 30 minutes to allow the sample to clot prior to centrifugation. The serum fraction can be separated by placing the collection tube into a room-temperature (18 to 25° C.), horizontal rotor (with a swing-out head) for 15 minutes at 1000 to 2500 RCF. Immediately following the completion of centrifugation, the serum fraction can be withdrawn by pipette and divided into 2 polypropylene freezing tubes (with each tube receiving approximately equal aliquots).
After processing, samples can be placed into a freezer at approximately −70° C. Repeated freeze-thaw cycles should be avoided.
Serum Tumor Markers: Serum may be obtained for assessment of the circulating tumor markers, CEA and CA27.29, prior to initial administration of a Compound, and at other times as clinically relevant.
Tumor Perfusion Study With DCE-MRI: All subjects who are found to have at least one measurable or assessable lesion may undergo DCE-MRI (Liu et al., 2005, J. Clin. Oncol. 23(24): 5464-5473) for the target lesion of interest prior to initial administration of a Compound, and at other times as clinically relevant.
Tumor Metabolism Study With FDG-PET: All subjects may undergo FDG-PET (Weber et al., 2003, J. Clin. Oncol. 21(14): 2641-2657) for the target lesion of interest prior to initial administration of a Compound, and at other times as clinically relevant. FDG-PET scanning may also be used in conjunction with CT scanning for tumor evaluations.
Radiological Tumor Assessment: The determination of antitumor efficacy may be based on objective tumor assessments made according to the RECIST system of unidimensional evaluation and treatment decisions by the clinicians may be based on these assessments.
Method of Assessment: The same method of assessment and the same technique should be used to characterize each identified and reported lesion at baseline and during follow-up. Imaging-based evaluation is preferred to evaluation by clinical examination when both methods have been used to assess the anti-tumor effect of treatment.
CT, CT/positron emission tomography (PET), or MRI scans are the preferred methods for tumor assessments. CT, CT/PET, or MRI can be performed with cuts of 10 mm or less in slice thickness contiguously. This applies to the chest, abdomen, and pelvis.
Chest x-ray is acceptable as a method to measure pulmonary lesions when they are clearly defined and surrounded by aerated lung. However, chest CT or CT/PET is preferable for assessment of pulmonary lesions.
Clinical lesions may only be considered measurable when they are superficial (e.g., skin nodules, palpable lymph nodes). In the case of skin lesions, documentation by color photography including a ruler to estimate the size of the lesion is recommended.
Ultrasound may not be used to measure tumor lesions that are clinically not easily accessible for objective response evaluation, e.g., visceral lesions. However, it is an alternative to clinical measurements of superficial palpable nodes, subcutaneous lesions, and thyroid nodules. Ultrasound might also be useful to confirm the complete disappearance of superficial lesions usually assessed by clinical examination.
A tumor marker (eg, CEA, CA27.29, etc.) may not be used alone as a primary assessment of response or progression of disease. However, tumor markers that are being followed regularly must normalize in order for a complete response (CR) to be scored.
Endoscopy, laparoscopy, or radionuclide scan should not be used for response assessment.
Measurability of Tumor Lesions: At baseline, tumor lesions may be categorized by a clinician as measurable or non-measurable by the RECIST as described below.
Recording Tumor Measurements: All measurable lesions up to a maximum of 10 lesions representative of all involved organs may be identified as target lesions, and measured and recorded at baseline and at the stipulated intervals during treatment. Target lesions can be selected on the basis of their size (lesion with the longest diameters) and their suitability for accurate repetitive measurements (either by imaging techniques or clinically).
The longest diameter can be recorded for each target lesion. The sum of the longest diameter for all target lesions may be calculated and recorded as the baseline sum longest diameter to be used as reference to further characterize the objective tumor response of the measurable dimension of the disease during treatment. All measurements can be performed using a caliper or ruler and should be recorded in centimeters.
All other lesions (or sites of disease) can be identified as non-target lesions and should also be recorded at baseline. Measurements are not required and these lesions can be followed as “present” or “absent.”
Target Lesions:
Non-Target Lesions:
The cytological confirmation of the neoplastic origin of any effusion that appears or worsens during treatment when the measurable tumor has met criteria for response or SD may be important to differentiate between response or SD and PD.
Confirmation of Tumor Response: To be assigned a status of CR or PR, changes in tumor measurements in subjects with responding tumors should be confirmed by repeat studies that should be performed ≧3 weeks after the criteria for response are first met. In the case of SD, follow-up measurements should have met the SD criteria at least once after study entry at a minimum interval of 6 weeks.
Determination of Overall Response by RECIST: When both target and non-target lesions are present, individual assessments can be recorded separately. The overall assessment of response can involve all parameters as depicted in Table 29.
aMeasurable lesions only
bMay include measurable lesions not followed as target lesions or non-measurable lesions
cMeasurable or non-measurable lesions
The best overall response is the best response recorded from the start of the treatment until disease progression/recurrence (taking as reference for tumor progression the smallest measurements recorded since the treatment started). The subject's best response assignment may depend on the achievement of both measurement and confirmation criteria.
Subjects may be defined as being not evaluable for response if there is no post randomization oncologic assessment. These subjects may be counted as failures in the analysis of tumor response data.
In some circumstances, it may be difficult to distinguish residual disease from normal tissue. When the evaluation of a CR depends upon this determination, it is recommended that the residual lesion be investigated by fine needle aspirate or biopsy before confirming the CR status.
Results:
12.1 Combination Treatment with Paclitaxel in an Aggressive MCF-7 Estrogen-Sensitive Breast Cancer Xenograft Model
This example demonstrates that Compound #10 shows anti-tumor activity in an aggressive MCF-7 estrogen-sensitive breast cancer xenograft model and that the anti-tumor activity of Compound #10 can be complemented by paclitaxel.
Experimental Design. Aggressively growing, estrogen-sensitive MCF 7 breast cancer cells (hereafter referred to as MCF-7p) were passaged in vivo prior to use to generate a more aggressive cell line. Tumors were excised from donor mice, passed through a sterile mesh, and suspended in 0.9% sodium chloride, and 20 mg of this suspension was mixed 1:1 with Matrigel™. These tumor fragments were implanted subcutaneously into female athymic nude mice bearing estrogen pellets (0.72 mg/pellet) that had been inserted 2 days previously. After 28 days, when the tumors had become established and grown to a substantial size (i.e., the mean tumor size had reached ˜430 mm3), mice were divided into 4 groups, and treatment was administered as shown in Table 30.
aIn all animal groups, oral vehicle was L21 (35% Labrasol, 35% Labrafac, and 30% Solutol) and IV vehicle was saline.
bCompound #10 and/or L21 vehicle were administered by oral gavage QD continuously through 72 days. Paclitaxel and/or saline vehicle were administered IV on Days 2, 5, 9, 12, and 15.
Tumor size was measured by calipers at periodic intervals during the study. After tumors in a given group had reached an average size of ˜1500 mm3, the mice in that group were sacrificed; after 72 days of treatment, any remaining groups were taken off study.
Results. Results by treatment regimen are shown in Table 31. In vehicle-treated mice, tumors grew rapidly and these animals were all removed from study by Day 26. Paclitaxel alone induced transient cytoreduction and a tumor growth delay while Compound #10 alone substantially delayed tumor growth. When given in combination, paclitaxel and Compound #10 induced tumor regression and then prevented tumor regrowth. The enhanced combination activity with paclitaxel observed indicates that the actions of Compound #10 and paclitaxel can be complementary. In observing the animals, there was no evidence of toxicity associated with single agent Compound #10 treatment. The combination therapy was also well tolerated, with no evidence of enhanced toxicity relative to the control or to the paclitaxel alone treatment groups.
aIn all animal groups, oral vehicle was L21 (35% Labrasol, 35% Labrafac, and 30% Solutol) and IV vehicle was saline.
bCompound #10 and/or L21 vehicle were administered by oral gavage QD continuously through 72 days. Paclitaxel and/or saline vehicle were administered IV on Days 2, 5, 9, 12, and 15.
cDay 26 was the day on which vehicle-treated animals were sacrificed.
12.2 Inhibition of Tumor Growth in Combination with Tamoxifen in an MCF-7 Estrogen-Sensitive Breast Cancer Xenograft Model
This example demonstrates that Compound #10 shows anti-tumor activity in an MCF-7 estrogen-sensitive breast cancer xenograft model and that the anti-tumor activity of Compound #10 is complemented by the selective estrogen receptor modulator, tamoxifen.
Experimental Design. The estrogen-sensitive breast cancer cell, MCF-7, was passaged in vitro and the cells (5×106 cells/mouse mixed 1:1 with Matrigel™) were implanted subcutaneously in female athymic nude mice. Estrogen pellets (0.72 mg/pellet) were implanted in the mice 9 days prior to cell implantation. After 7 days, when the tumors had become established (i.e., the mean tumor size had reached 135 mm3), mice were divided into 4 groups, and treatment was administered as shown in Table 32.
aVehicle was L21 (35% Labrasol, 35% Labrafac, and 30% Solutol) and/or PEG-300.
bL21 was administered by oral gavage BID on Monday through Friday and QD on Saturday and Sunday for a total of 17 days; all morning doses were given before 0830; evening doses were administered at ≧1630 (i.e., ≧8 hours after the morning dose); thereafter, all doses were administered QD continuously for 25 days. PEG-300 was administered by oral gavage QD continuously for 42 days. Compound #10 was administered by oral gavage at 3 mg/kg BID on Monday through Friday and at 10 mg/kg QD on Saturday and Sunday for a total of 17 days; all morning doses were given before 0830; evening doses were administered at ≧1630 (i.e., ≧8 hours after the morning dose); thereafter, all doses were administered at 10 mg/kg QD continuously for 25 days. Tamoxifen was administered by oral gavage at 10 mg/kg QD continuously for 42 days.
Tumor size was measured by calipers at periodic intervals during the study. After 42 days of treatment, the mice were sacrificed.
Results. Results by treatment regimen are shown in Table 33. In vehicle-treated mice, tumors grew slowly. Two of 10 (20%) vehicle-treated mice were cured. In mice treated with tamoxifen alone, tumor regression and growth delay were observed, and 7 of the 10 (70%) mice were cured. Similarly, in mice treated with Compound #10 alone, tumor regression and growth delay compared favorably to that observed in tamoxifen treated mice, and 5 of the 10 (50%) mice were cured. In mice receiving combination therapy, tumor regression was even more rapid than that observed in mice treated with either agent as monotherapy, and 8 of 10 (80%) mice were cured. In observing the animals, there was no evidence of toxicity associated with any of the treatments.
aVehicle was L21 (35% Labrasol, 35% Labrafac, and 30% Solutol).
bCompound #10 and/or vehicle were administered by oral gavage at 3 mg/kg BID on Monday through Friday and at 10 mg/kg QD on Saturday and Sunday for a total of 17 days. All morning doses were given before 0830. Evening doses were administered at ≧1630 (i.e., ≧8 hours after the morning dose). Thereafter, all doses were administered at 10 mg/kg QD continuously for 25 days. Tamoxifen and/or vehicle were administered by oral gavage at 10 mg/kg QD continuously for 42 days.
cDay 42 was the day on which mice were sacrificed.
dCure was defined as a tumor too small to measure (typically ≦125 mm3 in this study).
12.3 Combination Treatment with Tamoxifen in an Aggressive MCF-7p Estrogen-Sensitive Breast Cancer Xenograft Model
This example demonstrates that Compound #10 shows anti-tumor activity in an aggressive MCF-7p estrogen-sensitive breast cancer xenograft model and that the anti-tumor activity of Compound #10 is complemented by the selective estrogen receptor modulator, tamoxifen.
Aggressively growing, estrogen-sensitive MCF 7 breast cancer cells (hereafter referred to as MCF-7p) were passaged in vivo prior to use to generate a more aggressive cell line. Tumors were excised from donor mice, passed through a sterile mesh, and suspended in 0.9% sodium chloride, and 20 mg of this suspension was mixed 1:1 with Matrigel™. These tumor fragments were implanted subcutaneously into female athymic nude mice bearing estrogen pellets (0.72 mg/pellet) that had been inserted 2 days previously. After 28 days, when the tumors had become established and grown to a substantial size (i.e., the mean tumor size had reached ˜435 mm3), mice were divided into 4 groups, and treatment was administered as shown in Table 34.
aVehicle for tamoxifen was PEG-300. Vehicle for Compound #10 was L21 (35% Labrasol, 35% Labrafac, and 30% Solutol).
bCompound #10 and/or vehicle were administered by oral gavage at 8 mg/kg QD continuously for 72 days. Tamoxifen and/or vehicle were administered by oral gavage at 8 mg/kg QD continuously for 72 days.
Tumor size was measured by calipers at periodic intervals during the study. When the mean tumor size in a group had reached 1500 mm3, or after 72 days of treatment, the mice in the group were sacrificed.
Results. Results by treatment regimen are shown in Table 35. In vehicle-treated mice, tumors grew rapidly and these animals were all removed from study by Day 26. Tamoxifen alone only modestly delayed tumor growth while Compound #10 alone showed a protracted tumor growth delay. With the combination of tamoxifen and Compound #10, mean tumor size was almost entirely static throughout the course of the experiment, substantially prolonging the mean time to tumor size ≧1000 mm3. In observing the animals, there was no evidence of toxicity associated with Compound #10 treatment or with the combination therapy.
aVehicle for tamoxifen was PEG-300. Vehicle for Compound #10 was L21 (35% Labrasol, 35% Labrafac, and 30% Solutol).
bCompound #10 and/or vehicle were administered by oral gavage at 8 mg/kg QD continuously for 72 days. Tamoxifen and/or vehicle were administered by oral gavage at 8 mg/kg QD continuously for 72 days.
cDay 26 was the day on which vehicle-treated animals were sacrificed.
12.4 Combination Treatment with Letrozole in an Aromatase Overexpressing MCF 7 Estrogen Sensitive Breast Cancer Xenograft Model
The example demonstrates that Compound #10 has anti-tumor activity in an aromatase-overexpressing, estrogen-sensitive MCF-7 breast cancer xenograft model.
Experimental Design. Aromatase-overexpressing, estrogen-sensitive MCF-7 cells (7.0×106 cells/mouse) were implanted subcutaneously in ovariectomized female athymic nude mice. Androstenedione pellets (6 mg/pellet) were implanted 1 day prior to cell implantation. After 28 days, when the tumors had become established (i.e., the mean tumor size had reached ˜200 mm3), mice were divided into 6 treatment groups (including low dose and high dose groups for letrozole, alone and in combination with Compound #10), and treatment was administered as shown in Table 36.
aVehicle was L21 (35% Labrasol, 35% Labrafac, and 30% Solutol).
bTreatments were administered by oral gavage QD continuously for 98 days.
Tumor size was measured by calipers at periodic intervals during the study. When the individual tumor size in a mouse exceeded 1500 mm3, or after 98 days of treatment, that mouse was sacrificed.
Results. Results by treatment regimen are shown in Table 37. In vehicle-treated mice, the first mouse was removed from study on Day 42; at this point, the average tumor size in vehicle-treated mice was ˜800 mm3. In mice treated with low-dose letrozole, tumor growth was prevented but tumor reduction was not observed. In mice treated with high-dose letrozole, tumor regression was observed. Throughout the study, the mean tumor reduction with Compound #10 was greater than that observed with high-dose letrozole. Because Compound #10 was so effective and induced cures in so many animals, no further effect could be observed when letrozole was combined with Compound #10. In observing the animals, there was no evidence of toxicity associated with any of the treatments.
aVehicle was L21 (35% Labrasol, 35% Labrafac, and 30% Solutol).
bTreatments were administered by oral gavage QD until the individual tumor size in a mouse exceeded 1500 mm3 or for 98 days.
cDay 42 was the day on which the first vehicle-treated animal was sacrificed.
dCure is defined as a tumor too small to measure (typically ≦75 mm3 in this experiment).
12.5 Combination Treatment with Bevacizumab in an MDA-MB-468 Estrogen-Insensitive Breast Cancer Xenograft Model
This example demonstrates the anti-tumor activity of Compound #10 alone and in combination bevacizumab (Avastin®) in an MDA MB 468 estrogen-insensitive breast cancer xenograft.
Experimental Design. Estrogen-insensitive breast cancer MDA MB 468 cells (5×106 cells/mouse mixed 1:1 with Matrigel™) were implanted subcutaneously in female athymic nude mice. After 6 days, when the tumors had become established (i.e., the mean tumor size had reached ˜185 mm3), mice were divided into 4 groups, and treatment was administered as shown in Table 38.
aVehicle was L21 (35% Labrasol, 35% Labrafac, and 30% Solutol) administered orally and saline administered IP.
bVehicle was administered by oral gavage QD continuously (L21) and by IP 2 times per week (saline) for at least 30 days. Compound #10 was administered by oral gavage QD continuously for at least 30 days. Bevacizumab was administered by IP 2 times per week for at least 30 days.
Tumor size was measured by calipers at periodic intervals during the study. When the individual tumor size in a mouse was between 1000 to 1500 mm3, that mouse was sacrificed and both tumor and plasma cells were assayed for VEGF concentration.
Results. Results by treatment regimen are shown in Table 39. Tumors reached more than 1500 mm3 by 15 days of treatment. Compound #10 significantly reduced intratumoral and plasma VEGF concentrations on the day on which the animals were sacrificed (range, Day 33 to 53) relative to controls (range, Day 9 to 15). In addition, Compound #10 reduced tumor size and prolonged the time to tumor progression (i.e., the time to reach ≧1000 mm3). Although less effective at inducing tumor growth delay than Compound #10, bevacizumab significantly reduced intratumoral and plasma VEGF concentrations on the day when the animals were sacrificed (range, Day 9 to 25). With this cell line, the magnitude of Compound #10 effect on tumor growth delay was such that the combination of bevacizumab with Compound #10 was no more effective than treatment with Compound #10 alone. In observing the animals, there was no evidence of toxicity associated with any of the treatments.
The invention is not to be limited in scope by the specific embodiments described herein. Indeed, various modifications of the invention in addition to those described will become apparent to those skilled in the art from the foregoing description and accompanying figures. Such modifications are intended to fall within the scope of the appended claims.
All references cited herein are incorporated herein by reference in their entirety and for all purposes to the same extent as if each individual publication or patent or patent application was specifically and individually indicated to be incorporated by reference in its entirety for all purposes.
This application claims the benefit of priority to U.S. Provisional Patent Application Ser. No. 61/181,653 entitled: METHODS FOR TREATING CANCER AND NON-NEOPLASTIC CONDITIONS, filed May 27, 2009; and, U.S. Provisional Patent Application 61/253,086 entitled: METHODS FOR TREATING BREAST CANCER, filed Oct. 20, 2009, each of which are incorporated herein by reference in their entirety and for all purposes.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/US10/36387 | 5/27/2010 | WO | 00 | 3/23/2012 |
| Number | Date | Country | |
|---|---|---|---|
| 61181653 | May 2009 | US | |
| 61253086 | Oct 2009 | US |
