David F. Penson, Vanderbilt University Medical Center and Tennessee Valley Veterans Administration Medical Center Geriatric Research, Education, and Clinical Center; Raoul Concepcion, Urology Associates PC, Nashville, TN; Andrew J. Armstrong, Duke Cancer Institute, Duke University, Durham, NC; Neeraj Agarwal, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT; Carl Olsson, Icahn School of Medicine at Mount Sinai, New York, NY; Lawrence Karsh, The Urology Center of Colorado, Denver, CO; Curtis Dunshee, Urological Associates of Southern Arizona, Tucson, AZ; Fong Wang and Kenneth Wu, Medivation, San Francisco, CA; Andrew Krivoshik, Astellas Pharma Global Development, Northbrook, IL; De Phung, Astellas Pharma Global Development, Leiden, The Netherlands; and Celestia S. Higano, Fred Hutchinson Cancer Research Center, University of Washington, Seattle, WA.
J Clin Oncol. 2016 Jun 20;34(18):2098-106. doi: 10.1200/JCO.2015.64.9285. Epub 2016 Jan 25.
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.
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).
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.
Enzalutamide significantly reduced risk of prostate cancer progression or death compared with bicalutamide in patients with nonmetastatic or metastatic CRPC.
恩扎卢胺是一种强效的口服雄激素受体抑制剂,可改善化疗前和化疗后转移性去势抵抗性前列腺癌(CRPC)患者的生存。比卡鲁胺是非甾体类抗雄激素药物,广泛用于治疗非转移性或转移性 CRPC 患者。本随机、双盲、II 期研究比较了这些药物在 CRPC 患者中的疗效和安全性。
共有 396 例非转移性(n=139)或转移性(n=257)CRPC 患者被随机分配至恩扎卢胺 160mg/天(n=198)或比卡鲁胺 50mg/天(n=198)组。两组均继续接受雄激素剥夺治疗。主要终点为无进展生存期(PFS)。
与比卡鲁胺相比,恩扎卢胺降低了 76%的进展或死亡风险(风险比[HR],0.24;95%CI,0.18 至 0.32;P<.001)。恩扎卢胺组中位 PFS 为 19.4 个月,比卡鲁胺组为 5.7 个月。恩扎卢胺显著改善了所有关键次要终点:前列腺特异性抗原进展时间(HR,0.19;95%CI,0.14 至 0.26;P<.001);前列腺特异性抗原应答≥50%的患者比例(81%比 31%;P<.001);以及转移性患者的影像学 PFS(HR,0.32;95%CI,0.21 至 0.50;P<.001)。恩扎卢胺在非转移性和转移性亚组中均观察到获益。观察到的不良事件谱与 III 期恩扎卢胺试验一致。
与比卡鲁胺相比,恩扎卢胺可显著降低非转移性或转移性 CRPC 患者前列腺癌进展或死亡的风险。