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Enzalutamide treatment in patients with metastatic castration-resistant prostate cancer progressing after chemotherapy and abiraterone acetate.

Authors :
Thomsen, Frederik Birkebaek
Røder, Martin Andreas
Rathenborg, Per
Brasso, Klaus
Borre, Michael
Iversen, Peter
Source :
Scandinavian Journal of Urology (Taylor & Francis Ltd); Jun2014, Vol. 48 Issue 3, p268-275, 8p
Publication Year :
2014

Abstract

Objective. The aim of this study was to record prostate-specific antigen (PSA) response and overall survival (OS) for a group of metastatic castration-resistant prostate cancer (mCRPC) patients treated with enzalutamide following progression after abiraterone treatment in the post-chemotherapy setting. Material and methods. Twenty-four mCRPC patients with progression after abiraterone treatment following primary docetaxel therapy received enzalutamide 160 mg/day. The percentage PSA response was recorded following first line docetaxel, abiraterone and enzalutamide treatment. Fischer's exact test, Mann-Whitney U test and linear regression model were used to test for differences in PSA response. Results. All patients had a follow-up of at least 3 months. The median PSA response following 1 month of enzalutamide was -12% (range -56% to 76%), while the median best PSA response was -22% (-76% to 76%). Forty-six percent had a greater than 30% decrease in PSA. The PSA response to enzalutamide did not correlate with the number of prior cancer treatments ( p = 0.57), time from diagnosis to mCRPC ( p = 0.11) or prior response to docetaxel ( p = 0.67). However, patients treated with second line cabazitaxel had an inferior PSA response to enzalutamide ( p = 0.03), and there was a trend for the PSA response to abiraterone to correlate with the PSA response to the succeeding enzalutamide ( B = 0.22, p = 0.05). The median OS was 4.8 months. Conclusions. Previous abiraterone therapy is associated with a less marked fall in PSA following enzalutamide therapy in post-chemotherapy mCRPC patients compared with reported results in randomized trials. Larger prospective studies of sequencing are warranted. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
21681805
Volume :
48
Issue :
3
Database :
Complementary Index
Journal :
Scandinavian Journal of Urology (Taylor & Francis Ltd)
Publication Type :
Academic Journal
Accession number :
96016513
Full Text :
https://doi.org/10.3109/21681805.2013.860189