The PREVAIL Study: Primary Outcomes by Site and Extent of Baseline Disease for Enzalutamide-treated Men with Chemotherapy-naive Metastatic Castration-resistant Prostate Cancer

被引:68
|
作者
Evans, Christopher P. [1 ]
Higano, Celestia S. [2 ]
Keane, Thomas [3 ]
Andriole, Gerald [4 ]
Saad, Fred [5 ]
Iversen, Peter [6 ]
Miller, Kurt [7 ]
Kim, Choung-Soo [8 ]
Kimura, Go [9 ]
Armstrong, Andrew J. [10 ]
Sternberg, Cora N. [11 ]
Loriot, Yohann [12 ]
de Bono, Johann [13 ]
Noonberg, Sarah B. [14 ]
Mansbach, Hank [15 ]
Bhattacharya, Suman [16 ]
Perabo, Frank [17 ]
Beer, Tomasz M. [18 ]
Tombal, Bertrand [19 ]
机构
[1] UC Davis Comprehens Canc Ctr, Dept Urol, Sacramento, CA USA
[2] Univ Washington, Div Med Oncol, Seattle Canc Care Alliance, Seattle, WA 98195 USA
[3] Med Univ South Carolina, Dept Urol, Charleston, SC USA
[4] Washington Univ, Sch Med, Div Urol Surg, St Louis, MO USA
[5] Univ Montreal, Ctr Hlth, Dept Surg, Montreal, PQ, Canada
[6] Univ Copenhagen, Rigshosp, Copenhagen Prostate Canc Ctr, DK-1168 Copenhagen, Denmark
[7] Charite, Dept Urol, Berlin, Germany
[8] Asan Med Ctr, Dept Urol, Seoul, South Korea
[9] Nippon Med Coll Hosp, Dept Urol, Tokyo, Japan
[10] Duke Canc Inst, Div Med Oncol & Urol, Durham, NC USA
[11] San Camillo & Forlanini Hosp, Dept Med Oncol, Rome, Italy
[12] Inst Gustave Roussy, Dept Canc Med, Villejuif, France
[13] Royal Marsden Hosp, Inst Canc Res, Drug Dev Unit, London, England
[14] Medivation Inc, Dept Early Clin Dev, San Francisco, CA USA
[15] Medivation Inc, Dept Med Affairs, San Francisco, CA USA
[16] Medivation Inc, Dept Biostat, San Francisco, CA USA
[17] Astellas Pharma Inc, Northbrook, IL USA
[18] OHSU Knight Canc Inst, Dept Hematol & Med Oncol, Portland, OR USA
[19] Clin Univ St Luc, Dept Urol, Brussels, Belgium
关键词
Androgen receptor; Castration-resistant prostatic cancer; Enzalutamide; MITOXANTRONE PLUS PREDNISONE; SURVIVAL;
D O I
10.1016/j.eururo.2016.03.017
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Enzalutamide, an oral androgen receptor inhibitor, significantly improved overall survival (OS) and radiographic progression-free survival (rPFS) versus placebo in the PREVAIL trial of men with chemotherapy-naive metastatic castration-resistant prostate cancer. Objective: To assess the effects of enzalutamide versus placebo in patients from PREVAIL based on site and extent of baseline disease. Design, setting, and participants: One thousand seven hundred and seventeen asymptomatic or minimally symptomatic patients were randomized to enzalutamide (n = 872) or placebo (n = 845). Subgroup analyses included nonvisceral (only bone and/or nodal; n = 1513), visceral (lung and/or liver; n = 204), low-volume bone disease (< 4 bone metastases; n = 867), high-volume bone disease (>= 4 bone metastases; n = 850), lymph node only disease (n = 195). Intervention: Oral enzalutamide (160 mg) or placebo once daily while continuing androgen deprivation therapy. Outcome measurements and statistical analysis: Coprimary endpoints (rPFS, OS) were prospectively evaluated in nonvisceral and visceral subgroups. All other efficacy analyses were post hoc. Results and limitations: Enzalutamide improved rPFS versus placebo in patients with nonvisceral disease (hazard ratio [HR], 0.18; 95% confidence interval [CI], 0.14-0.22), visceral disease (HR, 0.28; 95% CI, 0.16-0.49), low-or high-volume bone disease (HR, 0.16; 95% CI, 0.11-0.22; HR, 0.22; 95% CI, 0.16-0.29, respectively), and lymph node only disease (HR, 0.09; 95% CI, 0.04-0.19). For OS, HRs favored enzalutamide (< 1) across all disease subgroups, although 95% CI was > 1 in patients with visceral disease (HR, 0.82; 95% CI, 0.55-1.23). Enzalutamide was well tolerated in patients with or without visceral disease. Conclusions: Enzalutamide provided clinically significant benefits in men with chemotherapy-naive metastatic castration-resistant prostate cancer, with or without visceral disease, low-or high-volume bone disease, or lymph node only disease. Patient summary: Patients with metastatic castration-resistant prostate cancer-including those with or without visceral disease or widespread bone disease-benefitted from enzalutamide, an active well-tolerated therapy. (C) 2016 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:675 / 683
页数:9
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