Patent Application
20230277546
The disclosure relates to an agent for suppressing recurrence and/or metastasis of cancer comprising a beta-blocker and being administered during a perioperative period of cancer surgery. Hereinafter the agent is also referred to as “the agent of the disclosure.”
Activation of sympathetic nerves has been thought to increase risk of cancer metastasis by promoting angiogenesis and vascular invasion of tumor cells (see Non-Patent Literature 1). Retrospective studies to evaluate effects of oral beta-blockers revealed that chronic administration of a beta-blocker prolonged Overall Survival (OS) or Progression Free Survival (PFS) and improved long-term prognosis in patients with breast cancer, non-small cell lung cancer, prostate cancer, ovarian cancer, and malignant melanoma (see Non-Patent Literatures 2 to 8). A meta-analysis revealed that beta-blockers effectively improved long-term overall survival (see Non-Patent Literature 9). Additionally, there was a clinical trial by a combination of a beta-blocker for oral administration and a COX-2 inhibitor (see Non-Patent Literatures 10 and 11). On the contrary, it was also reported that administration of a beta blocker during a perioperative period did not improve recurrence-free survival rate or overall survival rate in patients with lung cancer (see Non-Patent Literature 12).
Landiolol hydrochloride (trade name: ONOACT), a compound disclosed in Patent Literature 1, has been known as a short-acting selective β1-blocker and has been primarily approved and marketed as a medicament for modulating heart rate in tachyarrhythmia.
One of the objects of the disclosure is to provide an agent for suppressing recurrence and/or metastasis of cancer.
The inventors found that postsurgical recurrence and/or metastasis of cancer is suppressed by administering a beta-blocker to a cancer patient during a perioperative period of cancer surgery.
Accordingly, the disclosure relates to the aspects including;
According to the disclosure, postsurgical recurrence and/or metastasis of cancer can be suppressed by administering a beta-blocker to a cancer patient during a perioperative period.
Unless otherwise defined, the terms used herein are read as generally understood by a skilled person in the technical fields such as organic chemistry, medicine, pharmacology, molecular biology, and microbiology. Definitions of several terms used herein are described below. The definitions herein take precedence over the general understanding.
When a numerical value is accompanied with the term “about”, the value is intended to represent any value within the range of ±10% of that value. For example, “about 20” means “a value between 18 and 22.” A range defined with a value of the lower limit and a value of the upper limit covers all values between the both values of the limits, including the values of the both limits. When a range is accompanied with the term “about”, the both limits are read as accompanied with the term. For example, “about 20 to 30” is read as “18 to 33.”
The term “beta-blocker” as used herein means a substance to block the β1-, β2-, or β3-adrenergic receptor in sympathetic nerves, including, but not limited to, landiolol, esmolol, propranolol, metoprolol, bisoprolol, acebutolol, atenolol, bufetolol, arotinolol, carteolol, pindolol, alprenolol, sotalol, nadolol, bopindolol, timolol, indenolol, bunitrolol, penbutolol, nipradilol, tilisolol, celiprolol, betaxolol, practolol, carvedilol, amosulalol, labetalol, bevantolol, oxprenolol, and levobunolol, as well as a salt thereof. Short-acting beta-blockers include, for example, landiolol, esmolol or a salt thereof, preferably landiolol hydrochloride or esmolol hydrochloride, more preferably landiolol hydrochloride. Intravenous beta-blockers include, for example, landiolol, esmolol, propranolol, labetalol, sotalol, metoprolol, or a salt thereof, preferably landiolol hydrochloride, esmolol hydrochloride, propranolol hydrochloride, labetalol hydrochloride, sotalol hydrochloride, or metoprolol tartrate, more preferably landiolol hydrochloride or esmolol hydrochloride, most preferably landiolol hydrochloride. Transdermal beta-blockers include bisoprolol or a salt thereof.
The salts as used herein are preferably pharmaceutically acceptable salts, especially pharmaceutically acceptable and water soluble salts. The pharmaceutically acceptable salts include alkali metal salts (e.g., potassium salts and sodium salts), alkaline earth metal salts (e.g., calcium salts and magnesium salts), ammonium salts, salts of pharmaceutically acceptable organic amines (e.g., tetramethyl ammonium, triethylamine, methylamine, dimethylamine, cyclopentylamine, benzylamine, phenethylamine, piperidine, monoethanolamine, diethanolamine, tris(hydroxymethyl)aminomethane, lysin, arginine, and N-methyl-D-glucamine), acid addition salts (e.g., salts of inorganic acids, such as hydrochlorides, hydrobromides, hydroiodides, sulfates, phosphates, and nitrates, as well as salts of organic acids, such as acetates, trifluoroacetates, lactates, tartrates, oxalates, fumarates, maleates, benzoates, citrates, methanesulfonates, ethanesulfonates, benzenesulfonates, toluenesulfonates, isethionates, glucoronates, and gluconates).
The beta-blockers mentioned above can be used safely with sufficiently low toxicity, because they have been approved and marketed as medicaments.
Short-acting beta-blockers are preferred in view of the hemodynamics of the patients during the cancer surgery. Intravenous or transdermal beta-blockers are also preferred because they can be administered together with an anesthetic drug.
The term “perioperative period” as used herein means a time period during which a cancer surgical procedure is performed, including preoperative, intraoperative, and postoperative periods. Specifically, the preoperative period begins before anesthetic induction prior to the cancer surgery (resection), e.g., immediately before the anesthetic induction, and the postoperative period includes several days until the condition of the patient after the cancer resection becomes stable, e.g., one to seven days from the end of the surgery. For example, the perioperative period begins preoperatively and ends at the termination of the anesthetic administration or later. Generally, any biological reaction due to an invasive procedure, e.g., increased blood pressure or tachycardia, does not occur in the preoperative period, as the period is prior to the surgery.
The administration period of the agent of the disclosure is preferably a period that begins before the anesthetic induction and ends seven days after the surgery, a period that begins before the anesthetic induction and ends six days after the surgery, a period that begins before the anesthetic induction and ends five days after the surgery, a period that begins before the anesthetic induction and ends four days after the surgery, or a period that begins before the anesthetic induction, for example, immediately before the anesthetic induction, and ends three days after the surgery. Alternatively, it is possible to predetermine a maximum administration period and stop the administration before the end of the period, for example one or two days before the end, depending on, for example, age, weight, gender, or clinical history of the patient, type, stage, progression, or metastatic potential of the cancer, operative procedure, organ subjected to the surgery, or combined therapy. For example, when an administration period is defined as ending within three days from the end of the surgery, the actual administration period may begin before the anesthetic induction and end optionally one, two or three days after the surgery. In this context, a period that begins before the anesthetic induction and ends one day after the surgery means a period that begins at the first administration of a beta-blocker prior to the anesthetic induction and ends about 24 hours after the first administration. Similarly, a period that ends two, three, four, five, six, or seven days after the surgery means a period that ends about 48, about 72, about 96, about 120, about 144, or about 168 hours after the first administration of a beta-blocker prior to the anesthetic induction, respectively.
The term “continuous administration” or “continuously administered” as used herein means that a beta-blocker is administered so that the blood concentration of the active ingredient is in the effective range over the period that is required for enabling the active ingredient to exhibit the effect to suppress postsurgical recurrence and/or metastasis of cancer. For example, intravenous continuous administration means administering an effective amount of a beta-blocker for a certain period, and may be achieved by administering a beta-blocker, e.g., in the form of an intravenous formulation or a lyophilized formulation dissolved in water for injection, via a pump for continuous injection, e.g., an infusion pump or a syringe pump.
The continuous administration may be performed intermittently with one or more appropriate washout periods as desired.
Whenever a beta-blocker is administered during a perioperative period, it can suppress postsurgical recurrence and/or metastasis of cancer. It is not necessary to administer a beta-blocker at other timing or via an oral route.
A beta-blocker may be administered at a dosage similar to the effective dosage known in the art. When it is continuously administered, the dosage may be adjusted within a certain range while the heart rate and blood pressure are monitored. For example, when landiolol hydrochloride is continuously administered parenterally, for example intravenously, the dosage may be about 0.1 to 10 μg/kg/min. Specific dosage of landiolol hydrochloride may be about 0.1 μg/kg/min, about 0.2 μg/kg/min, about 0.3 μg/kg/min, about 0.4 μg/kg/min, about 0.5 μg/kg/min, about 0.6 μg/kg/min, about 0.7 μg/kg/min, about 0.8 μg/kg/min, about 0.9 μg/kg/min, about 1 μg/kg/min, about 1.5 μg/kg/min, about 2 μg/kg/min, about 2.5 μg/kg/min, about 3 μg/kg/min, about 3.5 μg/kg/min, about 4 μg/kg/min, about 4.5 μg/kg/min, about 5 μg/kg/min, about 6 μg/kg/min, about 7 μg/kg/min, about 8 μg/kg/min, about 9 μg/kg/min, about 10 μg/kg/min, about 20 μg/kg/min, about 30 μg/kg/min, or about 40 μg/kg/min. A preferred dosage range herein may be determined by employing one dosage from the above-mentioned dosages as the lower limit and another dosage as the upper limit. Examples of such dosage range include about 0.2 to 8 μg/kg/min, about 0.3 to 5 μg/kg/min, about 0.4 to 3 μg/kg/min, about 0.5 to 2.5 μg/kg/min, about 0.2 to 20 μg/kg/min, about 0.3 to 15 μg/kg/min, about 0.4 to 10 μg/kg/min, and about 0.5 to 5 μg/kg/min.
The agent for suppressing recurrence and/or metastasis of cancer is administered to a mammal, for example a human, that is suffered from cancer and is in the perioperative period of cancer surgery (e.g., resection).
The term “agent for suppressing recurrence and/or metastasis of cancer” as used herein, which is also referred to as “antirecurrent and/or antimetastatic agent”, means an agent capable of suppressing postsurgical recurrence and/or metastasis of cancer. The term “recurrence” of cancer means that cancer occurs again after the cancer was treated for example by surgery, including recurrence of primary cancer and further recurrence of recurrent cancer. The recurrence of cancer may be diagnosed by diagnostic imaging or biopsy analysis, or may be diagnosed when a symptom is aggravated. Organs where cancer recurs or is expected to recur include the organ where the cancer primarily occurred and any other organs. The term “metastasis” of cancer means recurrence of cancer in an organ other than the organ where the cancer primarily occurred. The term “suppressing recurrence and/or metastasis of cancer” includes preventing, reducing, or delaying recurrence and/or metastasis of cancer, or preventing, reducing, or delaying progression of cancer after recurrence and/or metastasis.
The term “cancer” as used herein includes solid tumors and hematologic tumors. The solid tumors include, for example, malignant melanoma (e.g., malignant melanoma in skin, oral mucosa epithelium, or orbit), non-small cell lung cancer (e.g., squamous non-small cell lung cancer or non-squamous non-small cell lung cancer), small cell lung cancer, head and neck cancer, brain tumor, renal cell cancer, clear cell renal cell cancer, breast cancer, ovarian cancer, ovarian clear cell adenocarcinoma, bone or soft tissue sarcoma (e.g., Ewing sarcoma, pediatric rhabdomyosarcoma, or uterine corpus leiomyosarcoma), glioblastoma, gliosarcoma, nasopharyngeal cancer, uterine cancer (e.g., uterine cervix cancer or endometrial cancer), anal cancer (e.g., anal canal cancer), colon cancer, hepatocellular cancer, biliary cancer, esophageal cancer, pancreatic cancer, gastric cancer, urothelial cancer (e.g., bladder cancer, upper urinary tract cancer, ureter cancer, renal pelvis cancer, or urethral cancer), prostate cancer, fallopian tube cancer, primary peritoneal cancer, pleural mesothelioma, and myeloproliferative syndrome, especially malignant melanoma, non-small cell lung cancer, small cell lung cancer, gastric cancer, pancreatic cancer, breast cancer, ovarian cancer, prostate cancer, renal cell cancer, colon cancer, esophageal cancer, hepatocellular cancer, brain tumor, head and neck cancer, and biliary cancer. The hematologic tumors include, for example, multiple myeloma, malignant lymphoma (e.g., non-Hodgkin's lymphoma, such as follicular lymphoma or diffuse large-B-cell lymphoma, or Hodgkin's lymphoma), and leukemia (e.g., acute myeloid leukemia or chronic myeloid leukemia).
The effect of the agent of the disclosure, i.e., the effect to suppress recurrence and/or metastasis of cancer, may be enhanced by using the agent in combination with an additional therapy such as a known anticancer agent, cell-based therapy, and/or radiotherapy. Examples of the known anticancer agent include alkylating agents, antimetabolites, anticancerous antibiotics, plant alkaloids, antihormones, platinum compounds, cytokine preparations, molecular target agents, cancer immunotherapeutic agents, and cancer vaccines. Examples of the cell-based therapy include hematopoietic stem cell transplantation and chimeric antigen receptor (CAR) T-cell therapy. Examples of the radiotherapy include proton beam therapy, heavy ion radiotherapy, and boron neutron capture therapy (BNCT). The additional therapy may be applied at any time according to the standard therapeutic schedule of the therapy, without limited to a perioperative period. That is, the additional therapy may be applied before, during, or after the surgery.
The agent of the disclosure and at least one other anticancer agent may be administered via a single preparation containing the both agents or multiple separate preparations containing each agent individually. The separate preparations may be administered simultaneously or at different time points. When the separate preparations are administered at different time points, the preparation containing the agent of the disclosure may be administered first and then the preparation containing the other anticancer agent may be administered, or the preparation containing the other anticancer agent may be administered first and then the preparation containing the agent of the disclosure may be administered. The administration routes of each preparation may be same or different. Two or more other anticancer agents may be used in combination. The other anticancer agent may be a known anticancer agent, or an anticancer agent which will be found in future and works in a mechanism similar to that of a known anticancer agent.
Examples of the alkylating agent include nitrogen mustard N-oxide hydrochloride, cyclophosphamide, ifosfamide, melphalan, thiotepa, carboquone, busulfan, nimustine hydrochloride, dacarbazine, ranimustine, carmustine, chlorambucil, bendamustine, and mechlorethamine.
Examples of the antimetabolite include TS-1 (registered trademark), methotrexate, mercaptopurine, 6-mercaptopurine riboside, fluorouracil, tegafur, tegafur-uracil, carmofur, doxifluridine, cytarabine, enocitabine, tegafur-gimestat-otastat potassium, gemcitabine hydrochloride, cytarabine ocfosphate, procarbazine hydrochloride, and hydroxycarbamide.
Examples of the anticancerous antibiotic include actinomycin D, mitomycin C, daunorubicin hydrochloride, doxorubicin hydrochloride, aclarubicin hydrochloride, neocarzinostatin, pirarubicin hydrochloride, epirubicin (hydrochloride), idarubicin hydrochloride, chromomycin A3, bleomycin (hydrochloride), peplomycin sulfate, therarubicin, zinostatin stimalamer, and gemtuzumab ozogamicin.
Examples of the plant alkaloid include vinblastine sulfate, vincristine sulfate, vindesine sulfate, irinotecan hydrochloride, etoposide, flutamide, vinorelbine ditartrate, docetaxel hydrate, and paclitaxel.
Examples of the antihormone include estramustine phosphate sodium, mepitiostane, epitiostanol, goserelin acetate, fosfestrol (diethylstilbestrol phosphate), tamoxifen citrate, toremifene citrate, fadrozole hydrochloride hydrate, medroxyprogesterone acetate, bicalutamide, leuprorelin acetate, anastrozole, aminoglutethimide, androgen bicalutamide, and fulvestrant.
Examples of the platinum compound include carboplatin, cisplatin, nedaplatin, and oxaliplatin.
Examples of the cytokine preparation include IFN-alfa-2a, IFN-alfa-2b, PEG-IFN-alfa-2b, interferon beta natural, and interleukin-2.
Examples of the molecular target agent include rituximab, ibritumomab, ibritumomab tiuxetan, ocrelizumab, ofatuzumab, obinutuzumab, alemtuzumab, imatinib, sorafenib, sunitinib, bevacizumab, gefitinib, erlotinib, crizotinib, temsirolimus, everolimus, axitinib, pazopanib, regorafenib, cetuximab, ibrutinib, panitumumab, lapatinib, trastuzumab, and vandetanib.
Examples of the cancer immunotherapeutic agent include anti-PD-1 antibodies (e.g., human anti-human PD-1 monoclonal (neutralizing) antibodies, such as nivolumab and REGN-2810, and humanized anti-human PD-1 monoclonal (neutralizing) antibodies, such as pembrolizumab, PDR-001, BGB-A317, AMP-514 (also known as MEDI0680), ANB011 (also known as TSR-042), and STI-A1110), anti-PD-L1 antibodies (e.g., atezolizumab (also known as RG7446 or MPDL3280A), avelumab (also known as PF-06834635 or MSB0010718C), durvalumab (also known as MEDI4736), BMS-936559, STI-1010, STI-1011, and STI-1014), PD-1 antagonists (e.g., AUNP-12), anti-PD-L2 antibodies, PD-L1 fusion proteins, PD-L2 fusion proteins (e.g., AMP-224), anti-CTLA-4 antibodies (e.g., ipilimumab and tremelimumab), anti-LAG-3 antibodies (e.g., BMS-986016 and LAG525), anti-Tim3 antibodies (e.g., MBG453), anti-KIR antibodies (e.g., lirilumab), anti-BTLA antibodies, anti-TIGIT antibodies, anti-VISTA antibodies, anti-CD137 antibodies (e.g., urelumab), anti-OX40 antibodies (e.g., MEDI6469), anti-HVEM antibodies, anti-CD27 antibodies (e.g., varlilumab), anti-GITR antibodies (e.g., MK-4166 and TRX-518), anti-CD28 antibodies, anti-CCR4 antibodies (e.g., mogamulizumab), anti-CD4 antibodies (e.g., MTRX-1011A, TRX-1, ibalizumab, huB-F5, zanolimumab, 4162W94, clenoliximab, keliximab, AD-519, PRO-542, cedelizumab, TNX-355, dacetuzumab, tregalizumab, priliximab, MDX-CD4, CAMPATH-9, and IT1208), TLR agonists, and STING agonists (e.g., MIW815).
Examples of the cancer vaccine include tumor antigen peptide vaccines and dendritic cell vaccines.
For example, the disclosure provides the following embodiments;
The entire contents of the documents cited herein are incorporated herein by reference. The embodiments described above are non-limiting and may be modified without deviating from the scope of the invention as defined by the appended claims. The following examples do not restrict or limit the invention and are for illustrative purposes only.
Ethics committee approval was obtained before the study was started. Among the patients who underwent lung lobectomy, the outcomes were compared between those who were treated with landiolol hydrochloride and those who were not treated with it.
For each patient the following information was drawn from the medical chart from May 2012 to Mar. 31, 2017 and recorded in clinical report form (CRF).
The 2-year recurrence-free survival rate was compared between the patients who had been treated with landiolol hydrochloride and the patients who had not been treated with it to evaluate the effect of landiolol hydrochloride.
Kaplan-Meier method as described below was employed to calculate the 2-year recurrence-free survival rate.
The recurrence was defined as follows;
The recurrence-free survival and the overall survival were compared between the patients who had been treated with landiolol hydrochloride and the patients who had not been treated with it to evaluate the effects of landiolol hydrochloride.
The recurrence-free survival and the overall survival were calculated according to the following equations;
The term “date of diagnosis of recurrence or date of death for any cause, whichever came earlier” is defined as below.
The patients who fulfilled all the following inclusion and exclusion criteria were included in the study.
Backgrounds of the patients obtained as described in item 1) of 2. Methods above are summarized in Table 1. Landiolol hydrochloride was administered to the patients in the test group by intravenous continuous administration at the dosage of 2.5 μg/kg/min over the period from the induction to completion of anesthesia. Saline was continuously administered to the patients in the control group (placebo group).
The primary endpoint, the 2-year recurrence-free survival rate, was compared between the test group and the control group as described in items 2)-1 and 2)-1-1 of 2. Methods above. The results are shown in Table 2. The 2-year recurrence-free survival rates were 89.3% and 75.9% in the test group and the control group, respectively.
a) *: p < 0.05, N.S.: p >= 0.05
There was a tendency that the administration of landiolol hydrochloride prolongs both of the recurrence-free survival and the overall survival.
These results indicate that administration of landiolol hydrochloride during a perioperative period of lung cancer surgery can suppress recurrence and/or metastasis of the cancer.
Patients with non-small cell lung cancer who will undergo surgery for complete resection of the cancer are involved in the study. For evaluating effectiveness and safety of landiolol hydrochloride in the patients, a multicenter, unblinded, randomized, controlled, investigator-initiated clinical trial is carried out as described below. The control group includes the patients who undergo the surgery but are not treated with landiolol hydrochloride.
Primary endpoints: recurrence-free survival (RFS) over first two postoperative years and overall survival (OS)
Secondary endpoints: <Effectiveness> For example, whether the patients are subjected to treatment of recurrence or not, and if subjected, the period until the treatment; the time until OS or the treatment of recurrence, <Safety> adverse events, incidence of postoperative complication, blood pressure, 12-lead electrocardiogram, and general laboratory test
Dosage: 2.5 μg/kg/min at the beginning and adjusted in the range of 0.5 to 5 μg/kg/min
Administration period: continuous intravenous administration is started immediately before the anesthetic induction and kept for 72 hours
The study confirms the effect of landiolol hydrochloride administered during a perioperative period of lung cancer surgery to suppress recurrence and/or metastasis of the cancer.
Recurrence and/or metastasis of cancer can be suppressed by administering a beta-blocker, preferably landiolol hydrochloride, to a cancer patient during a perioperative period of cancer surgery. This desired effect can be achieved with less burden on the patient because the beta-blocker is administered for the short perioperative period and no chronic administration is necessary.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2017-128968 | Jun 2017 | JP | national |
This application is Continuation of U.S. application Ser. No. 16/339,201, filed Apr. 3, 2019, which is National Stage of International Application No. PCT/JP2018/024782, filed Jun. 29, 2018, claiming priority to Japanese Patent Application No. 2017-128968, filed Jun. 30, 2017, the contents of all of which are incorporated herein by reference in their entirety.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 16339201 | Apr 2019 | US |
| Child | 18091666 | US |
