Taro Iguchi1, Satoshi Tamada2, Minoru Kato2, Sayaka Yasuda2, Yuichi Machida3, Tetsuji Ohmachi4, Keiichi Ishii5, Hiroyuki Iwata6, Shinji Yamamoto7, Tomohiro Kanamaru8, Kazuya Morimoto9, Taro Hase10, Koichiro Tashiro11, Koji Harimoto12, Takashi Deguchi13, Takahisa Adachi14, Katsuki Iwamoto15, Yoshinori Takegaki16, Tatsuya Nakatani2. 1. Department of Urology, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-ku, Osaka, 545-8585, Japan. taro@msic.med.osaka-cu.ac.jp. 2. Department of Urology, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-ku, Osaka, 545-8585, Japan. 3. Department of Urology, Yao Municipal Hospital, Yao, Japan. 4. Department of Urology, Bell-land General Hospital, Sakai, Japan. 5. Department of Urology, Osaka City General Hospital, Osaka, Japan. 6. Department of Urology, Itami City Hospital, Itami, Japan. 7. Department of Urology, Ikuwakai Memorial Hospital, Osaka, Japan. 8. Department of Urology, Yao Tokushukai General Hospital, Yao, Japan. 9. Department of Urology, Osaka General Hospital of West Japan Railway Company, Osaka, Japan. 10. Department of Urology, Suita Municipal Hospital, Suita, Japan. 11. Department of Urology, Meijibashi Hospital, Matsubara, Japan. 12. Department of Urology, Fuchu Hospital, Izumi, Japan. 13. Department of Urology, PL Hospital, Tondabayashi, Japan. 14. Department of Urology, Osaka City Juso Hospital, Osaka, Japan. 15. Department of Urology, Ishikiriseiki Hospital, Higashiosaka, Japan. 16. Department of Urology, Minamiosaka Hospital, Osaka, Japan.
Abstract
BACKGROUND: Before the androgen target therapy era, flutamide was widely used for castration-resistant prostate cancer in Japan. Enzalutamide is currently the recommended treatment; however, the efficacy and safety of enzalutamide and flutamide after combined androgen blockade therapy with bicalutamide, has not been compared. METHODS:Patients with castration-resistant prostate cancer who receivedcombined androgen blockade therapy with bicalutamide were randomly assigned to receive either enzalutamide or flutamide. The primary endpoint for efficacy was the 3-month prostate-specific antigen response rate. This trial is registered with ClinicalTrials.gov (NCT02346578) and the University hospital Medical Information Network (UMIN000016301). RESULTS: Overall, 103 patients were enrolled. The 3- (80.8% vs. 35.3%; p < 0.001) and 6-month (73.1% vs. 31.4%; p < 0.001) prostate-specific antigen response rates were higher in the enzalutamide than in the flutamide group. The 3-month disease progression rates (radiographic or prostate-specific antigen progression) were 6.4% and 38.8% in the enzalutamide and flutamide groups, respectively [hazard ratio (HR): 0.16; 95% confidence interval (CI): 0.05-0.47; p < 0.001]; the 6-month rates were 11.4% and 51.1%, respectively (HR 0.22; 95% CI 0.09-0.50; p < 0.001). Enzalutamide provided superior prostate-specific antigen progression-free survival compared with flutamide (HR 0.29; 95% CI 0.15-0.54; p < 0.001). Median time to prostate-specific antigen progression-free survival was not reached and was 6.6 months in the enzalutamide and flutamide groups, respectively. CONCLUSIONS: As an alternative anti-androgen therapy in patients with castration-resistant prostate cancer who failbicalutamide-combined androgen blockade therapy, enzalutamide provides superior clinical outcomes compared with flutamide. Enzalutamide should be preferred over flutamide in these patients.
RCT Entities:
BACKGROUND: Before the androgen target therapy era, flutamide was widely used for castration-resistant prostate cancer in Japan. Enzalutamide is currently the recommended treatment; however, the efficacy and safety of enzalutamide and flutamide after combined androgen blockade therapy with bicalutamide, has not been compared. METHODS:Patients with castration-resistant prostate cancer who received combined androgen blockade therapy with bicalutamide were randomly assigned to receive either enzalutamide or flutamide. The primary endpoint for efficacy was the 3-month prostate-specific antigen response rate. This trial is registered with ClinicalTrials.gov (NCT02346578) and the University hospital Medical Information Network (UMIN000016301). RESULTS: Overall, 103 patients were enrolled. The 3- (80.8% vs. 35.3%; p < 0.001) and 6-month (73.1% vs. 31.4%; p < 0.001) prostate-specific antigen response rates were higher in the enzalutamide than in the flutamide group. The 3-month disease progression rates (radiographic or prostate-specific antigen progression) were 6.4% and 38.8% in the enzalutamide and flutamide groups, respectively [hazard ratio (HR): 0.16; 95% confidence interval (CI): 0.05-0.47; p < 0.001]; the 6-month rates were 11.4% and 51.1%, respectively (HR 0.22; 95% CI 0.09-0.50; p < 0.001). Enzalutamide provided superior prostate-specific antigen progression-free survival compared with flutamide (HR 0.29; 95% CI 0.15-0.54; p < 0.001). Median time to prostate-specific antigen progression-free survival was not reached and was 6.6 months in the enzalutamide and flutamide groups, respectively. CONCLUSIONS: As an alternative anti-androgen therapy in patients with castration-resistant prostate cancer who fail bicalutamide-combined androgen blockade therapy, enzalutamide provides superior clinical outcomes compared with flutamide. Enzalutamide should be preferred over flutamide in these patients.
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