D Robert Siemens1, Laurence Klotz2, Axel Heidenreich3, Simon Chowdhury4, Arnauld Villers5, Benoit Baron6, Steve van Os6, Nahla Hasabou7, Fong Wang8, Ping Lin8, Neal D Shore9. 1. Centre for Applied Urological Research, Queen's University, Kingston, Ontario, Canada. Electronic address: siemensr@kgh.kari.net. 2. Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada. 3. Department of Urology, University of Cologne, Cologne, Germany. 4. Guy's, King's and St Thomas' Hospitals, London, United Kingdom. 5. Department of Urology, Lille University, Lille, France. 6. Astellas Pharma, Inc., Leiden, The Netherlands. 7. Astellas Pharma, Inc., Northbrook, Illinois, USA. 8. Medivation, Inc., which was acquired by Pfizer, Inc. in September 2016, San Francisco, California, USA. 9. Carolina Urologic Research Center, Myrtle Beach, South Carolina, USA.
Abstract
PURPOSE:Enzalutamide significantly prolonged median progression-free survival vs bicalutamide in chemotherapy naïve men with metastatic castration resistant prostate cancer in the TERRAIN (Enzalutamide versus Bicalutamide in Castrate Men with Metastatic Prostate Cancer) trial. In this post hoc analysis we investigated the influence of age on the efficacy and safety of enzalutamide vs bicalutamide in this population. MATERIALS AND METHODS: Patients were randomized 1:1 to enzalutamide 160 mg per day or bicalutamide 50 mg per day. Progression-free survival, time to prostate specific antigen progression and safety were analyzed post hoc in younger (age less than 75 years) and older (age 75 years or greater) subgroups. RESULTS:Enzalutamide significantly reduced the risk of disease progression or death vs bicalutamide in patients younger than 75 years (HR 0.38, 95% CI 0.27-0.52, p <0.0001) and 75 years old or older (HR 0.59, 95% CI 0.37-0.92, p = 0.018). Time to prostate specific antigen progression was also significantly prolonged with enzalutamide vs bicalutamide in each subgroup. The adverse event distribution between treatments was similar in each subgroup except for more (5% or greater difference between subgroups) atrial fibrillation, urinary tract infections, falls and decreased appetite as well as less extremity pain and hot flushing in enzalutamidetreated patients 75 years old or older, and less back pain and hot flushing inbicalutamidetreated patients 75 years old or older. Grade 3 or greater cardiac events were more frequent in enzalutamide treated and bicalutamidetreated patients who were 75 years old or older vs younger than 75 years. Fatigue was more frequent in enzalutamide treated patients with a similar distribution in each age subgroup. CONCLUSIONS:Enzalutamide improved clinical outcomes vs bicalutamide irrespective of age. Increased falls and cardiac events suggest caution when prescribing to older patients (age 75 years or greater) with significant comorbidity.
RCT Entities:
PURPOSE:Enzalutamide significantly prolonged median progression-free survival vs bicalutamide in chemotherapy naïve men with metastatic castration resistant prostate cancer in the TERRAIN (Enzalutamide versus Bicalutamide in Castrate Men with Metastatic Prostate Cancer) trial. In this post hoc analysis we investigated the influence of age on the efficacy and safety of enzalutamide vs bicalutamide in this population. MATERIALS AND METHODS:Patients were randomized 1:1 to enzalutamide 160 mg per day or bicalutamide 50 mg per day. Progression-free survival, time to prostate specific antigen progression and safety were analyzed post hoc in younger (age less than 75 years) and older (age 75 years or greater) subgroups. RESULTS:Enzalutamide significantly reduced the risk of disease progression or death vs bicalutamide in patients younger than 75 years (HR 0.38, 95% CI 0.27-0.52, p <0.0001) and 75 years old or older (HR 0.59, 95% CI 0.37-0.92, p = 0.018). Time to prostate specific antigen progression was also significantly prolonged with enzalutamide vs bicalutamide in each subgroup. The adverse event distribution between treatments was similar in each subgroup except for more (5% or greater difference between subgroups) atrial fibrillation, urinary tract infections, falls and decreased appetite as well as less extremity pain and hot flushing in enzalutamide treated patients 75 years old or older, and less back pain and hot flushing in bicalutamide treated patients 75 years old or older. Grade 3 or greater cardiac events were more frequent in enzalutamide treated and bicalutamide treated patients who were 75 years old or older vs younger than 75 years. Fatigue was more frequent in enzalutamide treated patients with a similar distribution in each age subgroup. CONCLUSIONS:Enzalutamide improved clinical outcomes vs bicalutamide irrespective of age. Increased falls and cardiac events suggest caution when prescribing to older patients (age 75 years or greater) with significant comorbidity.
Authors: Bodine P S I Belderbos; Ronald de Wit; Caly Chien; Anna Mitselos; Peter Hellemans; James Jiao; Margaret K Yu; Gerhardt Attard; Iurie Bulat; W Jeffrey Edenfield; Fred Saad Journal: Cancer Chemother Pharmacol Date: 2018-07-05 Impact factor: 3.333