Abstract

PurposeAndrogen deprivation therapy (ADT) is the mainstay for the management of metastatic prostate cancer. Available pharmaceutical ADTs include gonadotropin-releasing hormone (GnRH) agonists and antagonists. Here, real-world data are presented from the UK general practitioner Optimum Patient Care Research Database. The study investigated the hypothesis that GnRH antagonists have lower cardiac event rates than GnRH agonists.MethodsThe incidence of cardiac events following initiation of GnRH antagonist or agonist therapy was investigated in a population-based cohort study conducted in UK primary care between 2010 and 2017.ResultsAnalysis of real-world data from the UK primary care setting showed that relative risk of experiencing cardiac events was significantly lower with degarelix, a GnRH antagonist, compared with GnRH agonists (risk ratio: 0.39 [95% confidence interval 0.191, 0.799]; p = 0.01). Patients that received degarelix as first-line treatment switched treatment more frequently (33.7%), often to a GnRH agonist, than those who initiated treatment with a GnRH agonist (6.7–18.6%).ConclusionScreening for known or underlying vascular disease and identifying those at high risk of a cardiac event is important for risk mitigation in patients with prostate cancer receiving hormone therapy. The GnRH antagonist degarelix conferred a significantly lower risk of cardiac events than GnRH agonists. Prior to treatment, patients should be stratified based on level of cardiovascular (CV) risk, and appropriate lifestyle, and pharmacological interventions to mitigate CV risk should be recommended. CV risk factors and patient response to the intervention should be monitored at regular intervals.

Highlights

  • Prostate cancer accounts for ~ 20% of new cancer diagnoses in the USA and the EU, and is the most commonly diagnosed cancer in England [1,2,3]

  • The aims of the study were to investigate the incidence of cardiac events following initiation of gonadotropin-releasing hormone (GnRH) antagonist or GnRH agonist as therapy in patients with prostate cancer

  • The relative risk of experiencing any cardiac event was lower with degarelix than all GnRH agonists

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Summary

Introduction

Prostate cancer accounts for ~ 20% of new cancer diagnoses in the USA and the EU, and is the most commonly diagnosed cancer in England [1,2,3]. In the UK, there were around 47,700 new annual cases of prostate cancer from 2014 to 2016, 49,029 new annual cases in 2018, and incidence rates are estimated to rise by 12% between 2014 and 2035, to 233 cases per 100,000 men by 2035 [3]. In 2017, prostate cancer accounted for 14% of all cancer deaths in men in the UK [4]. Androgen deprivation therapy (ADT) is the mainstay for the management of metastatic prostate cancer, and surgical castration has been superseded by non-surgical therapies, which are the standard of care [5,6,7]. Available pharmaceutical ADTs include gonadotropin-releasing hormone (GnRH) agonists, such as leuprolide, goserelin, triptorelin and buserelin acetate, and more recently, GnRH antagonists, such as degarelix and abarelix (approved in Germany and The Netherlands) [5, 8]

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