Patent Application
20230330098
The present invention relates to the use of fenoldopam, its salts and/or derivatives for the treatment of hemolytic uremic syndrome (HUS), preferably in the form due to infection from Shiga-like toxin-producing Escherichia Coli and in the atypical form.
Hemolytic uremic syndrome (HUS) is a severe clinical condition characterized by platelet consumption, hemolysis and multi-organ hypoxic/ischemic damage (particularly kidney and brain). Its parainfectious variant (the most common form) results from a gastrointestinal infection (hemorrhagic enteritis) from Shiga-like toxin-producing Escherichia Coli (STEC) (1). Its incidence varies notably due to geographic and climatic elements and in Western countries it is the main cause of acute kidney failure in the paediatric age with an average incidence (referring to Northern Italy) of 5.5 cases per million in the paediatric population (2). Although the disease is more common in children, even adults can be susceptible to it as highlighted by a recent epidemic in Germany with more than 800 affected of which 88% were adults (3).
To date the disease is encumbered by a mortality rate of 3-5% and by a risk of major sequelae (neurological or renal) for life in a percentage that varies between 10 and 25% (4). Regardless of the final outcomes, the disease implies significant care-related burdens as in the acute phase more than 50% of patients require dialysis for a variable period of days or weeks, as well as often requiring resuscitative care (due to the neurological effects) and long or very long periods of hospitalization (5-9).
To date there are no specific treatments for hemolytic uremic syndrome from STEC and patient management relies on support measures only: red blood cell transfusions, antihypertensive therapy, dialysis, anticonvulsant drugs, respiratory and resuscitative care (10-13).
A strategy has recently been developed for managing fluids in patients affected by HUS that envisages the maximum expansion of the circulating volume to contrast the hypoxic/ischemic damage resulting from systemic thrombosis of the microcirculation. Such strategy has enabled fatality to be prevented and both acute complications of the disease, and long-term ones (neurological or renal) to be reduced, although they still remain high (14-19).
Considering the physiopathological basis of tissue damage in thrombotic microangiopathy, therefore also in HUS, it is plausible to consider that the vasodilation of the microcirculation can result in a further reduction in hypoxic/ischemic damage.
Fenoldopam, a dopamine receptor D1 partial agonist, is known for its vasodilatory properties (20).
To date, it has usually been used in its salt form, Fenoldopam mesylate (see
Fenoldopam mesylate is found on the market as an injectable preparation, containing the active ingredient Fenoldopam mesylate but also water, citric acid, propylene glycol, sodium citrate dihydrate, sodium metabisulfite.
Fenoldopam mesylate is a fast-acting vasodilator and bonds with weak affinity to α2 adrenergic receptors. It does not have any affinity for D2, alpha1 and 5HT1 and 5HT2 or muscarinic receptors and the vascular response is not uniform in the different vascular systems.
The author of the present invention has now found that Fenoldopam can be advantageously used in the treatment of severe forms of hemolytic uremic syndrome from STEC in paediatric patients treated from the diagnosis of the disease until normal platelet levels are reached with the immediate observation of a significant improvement that has brought about fast recovery for patients without any of the common complications mentioned above.
In particular, it has been observed that in light of its specific vasodilatory action in the context of thrombotic microangiopathy, Fenoldopam can be considered the drug of choice in the treatment of hemolytic uremic syndrome.
The present document highlights the results obtained in the 12 patients affected by hemolytic uremic syndrome and subjected to treatment with Fenoldopam within the context of the therapeutic support procedures.
Therefore, the subject matter of the present invention is Fenoldopam or its salts for use in the medical field in the treatment of hemolytic uremic syndrome (HUS), preferably in the secondary form due to Shiga-like toxin-producing Escherichia Coli (STEC-HUS) or in the atypical form (HUSa). Due to the analogy between the pathogenetic mechanisms of the kidney failure in the two pathologies, also the patient who will be later diagnosed for atypical HUS (HUSa), can be advantageously treated firstly with Fenoldopam according to the present invention. According to a preferred embodiment, the population of patients affected by hemolytic uremic syndrome (HUS) is the paediatric population.
According to a preferred embodiment of the invention the fenoldopam salt used is fenoldopam mesylate.
The administration of fenoldopam for use in the treatment of hemolytic uremic syndrome (HUS) takes place through continuous intravenous infusion.
Preferably, the treatment takes place through infusion administration of a dose of fenoldopam (preferably fenoldopam mesylate) comprised in the range 0.05-0.3 mcg/kg/min, preferably 0.1 mcg/kg/min.
Even more preferably the patients affected by HUS to be treated with fenoldopam (preferably fenoldopam mesylate) are patients with HUS and platelet levels <150,000/mm3.
The subject matter of the present invention is also an injectable sterile aqueous solution comprising fenoldopam or its salts (preferably fenoldopam mesylate) together with one or more pharmaceutically acceptable excipients for use in the medical field in the treatment of hemolytic uremic syndrome, preferably from Shiga-like toxin-producing Escherichia Coli (STEC-HUS) or in the atypical form (HUSa).
According to a preferred embodiment of the present invention the injectable sterile aqueous solution for use in the treatment of hemolytic uremic syndrome is administered through the infusion of a dose of fenoldopam or its salts (preferably fenoldopam mesylate) comprised in the range 0.05-0.3 mcg/kg/min, preferably 0.1 mcg/kg/min.
The present invention will now be described, for non-limiting illustrative purposes, according to some preferred embodiments thereof, with particular reference to the attached figures, wherein:
In the following experimental section, the invention will be detailed according to a preferred embodiment. Such examples must not be considered as limiting for the purpose of the invention, but merely illustrative.
Patients and Methods
The (14) patients affected by HUS from STEC cared for at the HUS Centre of the IRCCS “Ca′ Granda Ospedale Maggiore Policlinico” Foundation in Milan were treated according to the invention with Fenoldopam mesylate starting from February 2017.
The Fenoldopam mesylate was administered in continuous infusion at a dosage comprised between 0.1-0.3 mcg/kg/min through peripheral vessel starting from the diagnosis of the disease.
For the purpose of the present analysis, hemolytic uremic syndrome from STEC was diagnosed by the concomitant presence of:
Cases of HUS associated with documented complement dysregulation and therefore treated as atypical HUS were excluded from the present analysis.
The patients included in the present study were also subjected to early circulating volume expansion according to the diagram previously described and published (14) to contrast hypoxic/ischemic damage.
In all the patients, treatment with Fenoldopam mesylate, and thus the infusion of isotonic fluids with the plasma, was always initiated within 3 hours of diagnosis of HUS from STEC (often before reaching our centre) and continued until improvement of the acute phase of the disease (platelet count >150,000/mm3).
The parents of all the patients were always informed as to the off-label nature of treatment with Fenoldopam and their informed consent for the treatment itself was acquired.
For the purpose of assessing the results obtained from the patient management procedure change, the following information was collected: personal data (age and gender), anthropometric data (weight), fundamental hematochemical data (hemoglobinemia, creatininemia, LDH and platelet count), clinical data (need for dialysis, neurological and/or other complications, need for ventilatory support, duration of hospitalization), hemodynamic data (renal resistive index both during treatment and after suspending treatment with Fenoldopam and again after recovery).
The data acquired was compared, retrospectively, with the natural course of the disease determined on 2 groups of patients already subject to previous analysis:
Statistical Analysis
The data is expressed as mean and confidence limits to the 95th percentile (CI), median and interquartile range according to the variables and their Gaussian distribution.
ANOVA and Chi-square were used to compare continuous and categorical variables, respectively, in the three groups.
The analyses were performed using the software Stata 13 (StataCorp. 2013, Stata: Release 13. Statistical Software. Collage Station, TX: Stata Corp.LP).
Results
During 2017, a total of 14 cases of hemolytic uremic syndrome were treated with Fenoldopam mesylate according to the protocol detailed above.
Two of such patients were then affected by atypical HUS and therefore were excluded from the present analysis.
The trial treatment with Fenoldopam in association with volume expansion of patients with hemolytic uremic syndrome from STEC was shown to be extremely useful in the preservation of kidney function in 10 of the 12 subjects treated, even if all of them were in the most acute phase of the disease.
Only 2 subjects (17%) needed dialytic support during the acute phase of the disease (vs. 55 and 35% in patients respectively with volume restriction and those treated with volume expansion only). Moreover, the subjects that needed dialysis required it for a very contained number of days with respect to the past (1 and 4 days). In a comparative analysis with respect to the 2 control groups, the mean days in dialysis which for the historic fluid restriction group was 4.9 (95th CI: 1.5-8.2) and in volume expansion only 2.4 (95th CI: 1.4-3.3), in the group treated with Fenoldopam it was 0.3 (CI: 0-1.1).
As highlighted in
Moreover, all this took place during clearly active disease conditions as shown by the platelet levels during the first days of disease that were constantly and severely dropping, indicating still very severe disease (see
The analysis of the real resistive index (
None of the children treated with Fenoldopam demonstrated any neurological effects during the acute phase, or permanent kidney or other damage. On this point, it is underlined that in the 2 compared groups, the nervous system involvement rate was 23.7% and 7.9% in relation to the restricted volume subjects and those exposed to expansion, while the permanent damage rate was 39.5% and 13.2% with 2 cases that led to patient death in the first group.
Finally, none of the children treated presented any side effects attributable to treatment with Fenoldopam mesylate.
In view of the initial difficulty of differential diagnosis between atypical HUS (HUSa) and HUS from STEC and the analogy of the pathogenetic mechanisms of the renal failure in the two pathologies, in later studies carried out in the years 2017-2018 also patients with atypical HUS were treated. Also in this case encouraging results were obtained, albeit the small group of treated patients.
More precisely, in three cases of HUSa (2 men and 1 woman) initially treated with Fenoldopam the natural course of the disease has been less aggressive of what generally observed, with the overall result that the patient reached the subsequent specific treatment with monoclonal antibody anti-CS, having accumulated less tissue damage, thus allowing a complete relief without permanent injuries. Therefore, also those patients who can later diagnosed for HUSa, can be advantageously be pretreated with Fenoldopam before starting with the specific therapy with anti-CS.
| Number | Date | Country | Kind |
|---|---|---|---|
| 102017000123899 | Oct 2017 | IT | national |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 16760407 | Apr 2020 | US |
| Child | 18139349 | US |
