Oncology
Prostate Cancer
Assessing Rapid Treatment Response in First-Line Metastatic Castration-Resistant Prostate Cancer (mCRPC)
Overview
Clinical Study Title:
Early Assessment of PSA Response in Patients With mCRPC Treated With Enzalutamide and Abiraterone
Clinical Study Abstract:
While resistance to abiraterone and enzalutamide in patients with metastatic castrate-resistant prostate cancer (mCRPC) has been well documented, little data exist on rates of rapid treatment response. Feibus et al conducted a single-institution retrospective review of PSA response in 123 mCRPC patients treated with abiraterone or enzalutamide.
A PSA response was achieved in 52/123 (42%) of patients taking abiraterone, with median time to PSA nadir of 37 days. Fifty-eight percent of patients responded to the drug within 4 weeks. PSA response to enzalutamide was achieved in 21/123 (17%) of patients, with a median time to PSA nadir of 140 days. Eighty-six percent of patients responded to the drug within 4 weeks.
The authors conclude that time to drug response and achievement of PSA decline can help predict long-term PSA response in patients with mCRPC.
Reference:
Feibus AH, Guccione JR, Vasudevamurthy A, et al. Early assessment of PSA response in patients with mCRPC treated with enzalutamide and abiraterone. J Clin Oncol. 2017;35 (suppl 6S; abstract e574).
Expert Commentary
Oliver Sartor, MD
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In Abstract e574, published at the 2017 American Society of Clinical Oncology Genitourinary Symposia by Feibus et al, a series of patients were analyzed for the rate of PSA decline after beginning abiraterone or enzalutamide. The patients were analyzed every 4 weeks rather than every 3 months as in the original phase 3 trials with these agents. For abiraterone, 68% of the patients who eventually responded with a 50% PSA decline had that 50% decline within 4 weeks. With enzalutamide, of the patients who responded to the drug, 86% responded within 4 weeks. The easiest way to interpret these data are that a response to enzalutamide, as measured by a 50% PSA decline, can be determined in the vast majority of patients after only 4 weeks on therapy. The data on abiraterone, however, are not nearly as reliable at 4 weeks. Additional data on early PSA declines (>50% decline) have been reported in abiraterone-treated patients by Facchini and colleagues (Front Pharmacol. 2016;7:123). They reported an early PSA response in 56% of patients evaluated at Day 15, and furthermore found that both progression-free survival and overall survival were improved for those with an early response. |