Enzalutamide Versus Bicalutamide in Castration-Resistant Prostate Cancer: The STRIVE Trial

被引:249
作者
Penson, David F. [1 ,2 ]
Armstrong, Andrew J. [4 ]
Concepcion, Raoul [3 ]
Agarwal, Neeraj [5 ]
Olsson, Carl [6 ]
Karsh, Lawrence [7 ]
Dunshee, Curtis [8 ]
Wang, Fong [9 ]
Wu, Kenneth [9 ]
Krivoshik, Andrew [10 ]
Phung, De [11 ]
Higano, Celestia S. [12 ]
机构
[1] Vanderbilt Univ, Med Ctr, Nashville, TN 37232 USA
[2] Tennessee Valley Vet Adm Med Ctr Geriatr Res, Educ & Clin Ctr, Nashville, TN USA
[3] Urol Associates PC, Nashville, TN USA
[4] Duke Univ, Duke Canc Inst, Durham, NC USA
[5] Univ Utah, Huntsman Canc Inst, Salt Lake City, UT USA
[6] Icahn Sch Med Mt Sinai, New York, NY 10029 USA
[7] Urol Ctr Colorado, Denver, CO USA
[8] Associates Southern Arizona, Urol, Tucson, AZ USA
[9] Medivation, San Francisco, CA USA
[10] Astellas Pharma Global Dev, Northbrook, IL USA
[11] Astellas Pharma Global Dev, Leiden, Netherlands
[12] Univ Washington, Fred Hutchinson Canc Res Ctr, Seattle, WA 98195 USA
关键词
WITHDRAWAL SYNDROME; INCREASED SURVIVAL; HORMONAL-THERAPY; CLINICAL-TRIALS; CHEMOTHERAPY; FLUTAMIDE; ANTIANDROGEN; COMBINATION; PROGRESSION; ABIRATERONE;
D O I
10.1200/JCO.2015.64.9285
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Enzalutamide, a potent oral androgen receptor inhibitor, improves survival in men with metastatic castration-resistant prostate cancer (CRPC) before and after chemotherapy. Bicalutamide, a nonsteroidal antiandrogen, is widely used to treat men with nonmetastatic or metastatic CRPC. The efficacy and safety of these drugs were compared in this randomized, double-blind, phase II study of men with CRPC. Patients and Methods A total of 396 men with nonmetastatic (n = 139) or metastatic (n = 257) CRPC were randomly assigned to enzalutamide 160 mg per day (n = 198) or bicalutamide 50 mg per day (n = 198). Androgen deprivation therapy was continued in both arms. The primary end point was progression-free survival (PFS). Results Enzalutamide reduced the risk of progression or death by 76% compared with bicalutamide (hazard ratio [HR], 0.24; 95% CI, 0.18 to 0.32; P < .001). Median PFS was 19.4 months with enzalutamide versus 5.7 months with bicalutamide. Enzalutamide resulted in significant improvements in all key secondary end points: time to prostate-specific antigen progression (HR, 0.19; 95% CI, 0.14 to 0.26; P < .001); proportion of patients with a >= 50% prostate-specific antigen response (81% v 31%; P < .001); and radiographic PFS in metastatic patients (HR, 0.32; 95% CI, 0.21 to 0.50; P < .001). Beneficial effects with enzalutamide were observed in both nonmetastatic and metastatic subgroups. The observed adverse event profile was consistent with that from phase III enzalutamide trials. Conclusion Enzalutamide significantly reduced risk of prostate cancer progression or death compared with bicalutamide in patients with nonmetastatic or metastatic CRPC. (C) 2016 by American Society of Clinical Oncology
引用
收藏
页码:2098 / +
页数:15
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