cARdiotoxicity Profile of aBIraTeRone in prostAte Cancer : a pharmacoviGilancE Study

Completed

• Conditions: Arrhythmias, Cardiac; Atrial Fibrillation and Flutter; Tachycardia, Supraventricular; Cardiac Failure

• Registration Number: NCT03243604
• Lead Sponsor: Groupe Hospitalier Pitie-Salpetriere

Brief Summary

Abiraterone associated with prednisone is used in prostate cancer. Abiraterone is a selective small-molecule inhibiting cytochrome P450 17A1 (CYP17A1), a key enzyme in androgen synthesis.

CYP17A inhibition is also responsible for mineral corticosteroid related adverse events as hypokaliemia, fluid retention, and hypertension. Primary hyperaldosteronism is associated with cardiovascular toxicities such as atrial fibrillation and cardiac failure. Other androgen-deprivation therapies are not associated with increased mineral corticosteroid level.

This study investigates reports of cardiovascular toxicities for treatment including L02 (sex hormones used in treatment of neoplastic diseases), and G03 (sex hormones) used in prostate cancer in the French pharmacovigilance database and in the EudraCT database.

Detailed Description

Due to its peculiar pharmacology, abiraterone is potentially associated with more cardiotoxicity as compared to other androgen-deprivation therapies. This study investigates the main characteristics of patients affected by cardiovascular side effects of which supraventricular arrhythmias (including atrial fibrillation, atrial flutter, supraventricular tachycardia), and cardiac failure imputed to drugs classified as L02, and G03 according to anatomical therapeutic chemical (ATC) classification. A causality assessment according to the World Health Organization-The Uppsala Monitoring Centre (WHO-UMC) is systematically applied.

Study Timeline

• Study Start: 2017-05-16
• Primary Completion: 2017-07-13
• Study Completion: 2017-07-13
• Study First Submitted: 2017-07-20
• Study First Submitted QC: 2017-08-04
• Study First Posted: 2017-08-09
• Status Verified: 2018-10
• Last Update Submitted: 2018-10-17
• Last Update Posted: 2018-10-18

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Male
• Target Recruitment: 1717

Inclusion Criteria

• Case reported in the French pharmacovigilance database from 01/01/1985 to 16/05/2017
• Case reported in the EudraCT database to May 2017
• Adverse event reported were including the MedDRA terms: SOC Cardiac Disorders; SOC Vascular Disorders; HLT Death, Sudden Death; HLGT Water, electrolyte and mineral investigations; HLGT Cardiac and vascular investigations (excl enzyme tests); and PT Syncope.
• Patients treated with hormonal therapies included in the ATC L02, and G03

Exclusion Criteria

• Chronology not compatible between the drug and the toxicity

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Analysis of disproportionality of reports for cardiotoxicity associated with abiraterone as compared to enzalutamide by performing a case- non-case study	2 months	Analysis of disproportionality of reports for cardiotoxicity associated with abiraterone as compared to enzalutamide by performing a case- non-case study

Secondary Outcome Measures

Name	Time	Method
Compare the reporting of suspected drug-induced supraventricular arrhythmias with abiraterone as compared to enzalutamide by performing a disproportionality analysis	2 months	Compare the reporting of suspected drug-induced supraventricular arrhythmias with abiraterone as compared to enzalutamide by performing a disproportionality analysis
Compare the reporting of drug-induced cardiac failure with abiraterone as compared to enzalutamide by performing a disproportionality analysis	2 months	Compare the reporting of drug-induced cardiac failure with abiraterone as compared to enzalutamide by performing a disproportionality analysis
Compare the reporting of drug-induced cardiac failure and/or supraventricular arrhythmias with abiraterone as compared to other androgen-deprivation therapies by performing a disproportionality analysis	2 months	Compare the reporting of drug-induced cardiac failure and/or supraventricular arrhythmias with abiraterone as compared to other androgen-deprivation therapies by performing a disproportionality analysis
Description of other mineralocorticoid related adverse events (hypokaliemia, fluid retention, and hypertension) when the cardio toxicity occurs	2 months	Description of other mineralocorticoid related adverse events (hypokaliemia, fluid retention, and hypertension) when the cardio toxicity occurs
Description of the population of patients having a cardio-vascular adverse event	2 months	Description of the population of patients having a cardio-vascular adverse event
Description of the drug-drug interactions associated with adverse events	2 months	Description of the drug-drug interactions associated with adverse events
Causality assessment of reported cardiovascular events according to the WHO-UMC system	2 months	Causality assessment of reported cardiovascular events according to the WHO-UMC system
Description of the duration of treatment when the toxicity happens (role of cumulative dose)	2 months	Description of the duration of treatment when the toxicity happens (role of cumulative dose)

Trial Locations

Locations (1)

Centre Régional de Pharmaco-vigilance - Paris, Pitié-Salpétrière; 🇫🇷 Paris, Ile De France, France