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Enzalutamide in Japanese patients with chemotherapy-naïve, metastatic castration-resistant prostate cancer: A post-hoc analysis of the placebo-controlled PREVAIL trial.

Authors :
Kimura G
Yonese J
Fukagai T
Kamba T
Nishimura K
Nozawa M
Mansbach H
Theeuwes A
Beer TM
Tombal B
Ueda T
Source :
International journal of urology : official journal of the Japanese Urological Association [Int J Urol] 2016 May; Vol. 23 (5), pp. 395-403. Date of Electronic Publication: 2016 Mar 27.
Publication Year :
2016

Abstract

Objectives: To evaluate the treatment effects, safety and pharmacokinetics of enzalutamide in Japanese patients.<br />Methods: This was a post-hoc analysis of the phase 3, double-blind, placebo-controlled PREVAIL trial. Asymptomatic or mildly symptomatic chemotherapy-naïve patients with metastatic castration-resistant prostate cancer progressing on androgen deprivation therapy were randomized one-to-one to 160 mg/day oral enzalutamide or placebo until discontinuation on radiographic progression or skeletal-related event and initiation of subsequent antineoplastic therapy. Coprimary end-points were centrally assessed radiographic progression-free survival and overall survival. Secondary end-points were investigator-assessed radiographic progression-free survival, time to initiation of chemotherapy, time to prostate-specific antigen progression, prostate-specific antigen response (≥50% decline) and time to skeletal-related event.<br />Results: Of 1717 patients, 61 were enrolled in Japan (enzalutamide, n = 28; placebo, n = 33); hazard ratios (95% confidence interval) of 0.30 for centrally assessed radiographic progression-free survival (0.03-2.95), 0.59 for overall survival (0.20-1.8), 0.46 for time to chemotherapy (0.22-0.96) and 0.36 for time to prostate-specific antigen progression (0.17-0.75) showed the treatment benefit of enzalutamide over the placebo. Prostate-specific antigen responses were observed in 60.7% of enzalutamide-treated men versus 21.2% of placebo-treated men. Plasma concentrations of enzalutamide were higher in Japanese patients: the geometric mean ratio of Japanese/non-Japanese patients was 1.126 (90% confidence interval 1.018-1.245) at 13 weeks. Treatment-related adverse events grade ≥3 occurred in 3.6% of enzalutamide- and 6.1% of placebo-treated Japanese patients.<br />Conclusion: Treatment effects and safety in Japanese patients were generally consistent with the overall results from PREVAIL.<br /> (© 2016 The Authors. International Journal of Urology published by John Wiley & Sons Australia, Ltd on behalf of the Japanese Urological Association.)

Details

Language :
English
ISSN :
1442-2042
Volume :
23
Issue :
5
Database :
MEDLINE
Journal :
International journal of urology : official journal of the Japanese Urological Association
Publication Type :
Academic Journal
Accession number :
27018069
Full Text :
https://doi.org/10.1111/iju.13072