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
相关论文
共 50 条
  • [31] Impact of Abiraterone Acetate and Enzalutamide on Symptom Burden of Patients with Chemotherapy-naive Metastatic Castration-resistant Prostate Cancer
    Salem, S.
    Komisarenko, M.
    Timilshina, N.
    Martin, L.
    Grewal, R.
    Alibhai, S.
    Finelli, A.
    CLINICAL ONCOLOGY, 2017, 29 (09) : 601 - 608
  • [32] Pharmacoeconomic aspects of using enzalutamide and abiraterone for treatment of chemotherapy-naive patients with metastatic castration-resistant prostate cancer
    Avxentyev, N. A.
    Frolov, M. Yu
    Makarova, Yu, V
    ONKOUROLOGIYA, 2019, 15 (02): : 86 - 99
  • [33] Cost-effectiveness analysis of enzalutamide for patients with chemotherapy-naive metastatic castration-resistant prostate cancer in Japan
    Okumura, Hiroyuki
    Inoue, Sachie
    Naidoo, Shevani
    Holmstrom, Stefan
    Akaza, Hideyuki
    JAPANESE JOURNAL OF CLINICAL ONCOLOGY, 2021, 51 (08) : 1319 - 1329
  • [34] Clinical Outcomes of Chemotherapy Naive Men with Metastatic Castration Resistant Prostate Cancer and Low Baseline Prostate Specific Antigen Treated with Enzalutamide vs Placebo
    Taplin, Mary-Ellen
    Armstrong, Andrew J.
    Lin, Ping
    Krivoshik, Andrew
    De Phung
    Parli, Teresa
    Tombal, Bertrand
    Beer, Tomasz M.
    JOURNAL OF UROLOGY, 2017, 198 (06): : 1325 - 1333
  • [35] Enzalutamide in Japanese patients with chemotherapy-naive, metastatic castration-resistant prostate cancer: A post-hoc analysis of the placebo-controlled PREVAIL trial
    Kimura, Go
    Yonese, Junji
    Fukagai, Takashi
    Kamba, Tomomi
    Nishimura, Kazuo
    Nozawa, Masahiro
    Mansbach, Hank
    Theeuwes, Ad
    Beer, Tomasz M.
    Tombal, Bertrand
    Ueda, Takeshi
    INTERNATIONAL JOURNAL OF UROLOGY, 2016, 23 (05) : 395 - 403
  • [36] Overall survival by race in chemotherapy-naive metastatic castration-resistant prostate cancer (mCRPC) patients treated with abiraterone acetate or enzalutamide.
    McNamara, Megan Ann
    George, Daniel J.
    Ramaswamy, Krishnan
    Lechpammer, Stanislav
    Mardekian, Jack
    Schultz, Neil M.
    Wang, Li
    Baser, Onur
    Huang, Ahong
    Freedland, Stephen J.
    JOURNAL OF CLINICAL ONCOLOGY, 2019, 37 (07)
  • [37] Enzalutamide in chemotherapy-naive metastatic castration-resistant prostate cancer in an Asian multiregional study: post hoc analysis of efficacy by baseline prostate-specific antigen levels
    Ahn, Hanjong
    Wang, Jianye
    Zhou, Fangjian
    Xia, Shu-Jie
    He, Dalin
    Yang, Yong
    Liu, Tong-Zu
    Kim, Janet
    Lee, Ai Ye Janise
    Pu, Yeong-Shiau
    INTERNATIONAL JOURNAL OF UROLOGY, 2020, 27 : 106 - 106
  • [38] Early PSA progression in abiraterone/enzalutamide-treated patients with metastatic castration-resistant prostate cancer.
    Lopez-Campos, Fernando
    Gomez-Iturriaga, Alfonso
    Llacer Perez, Casilda
    Henriquez, Ivan
    Peleteiro, Paula
    Lozano, Rebeca
    Castano, Ana
    Romero-Laorden, Nuria
    Molina-Cerrillo, Javier
    Alvarez-Rodriguez, Sara
    Piquer, Teresa
    Navarro-Castellon, Joaquin
    Jose Conde-Moreno, Antonio
    Ramirez-Backhaus, Miguel
    Barrionuevo, Patricia
    Garcia, Raquel
    de los Llanos Perez-Haro, Maria
    Castro, Elena
    Olmos, David
    Lorente, David
    JOURNAL OF CLINICAL ONCOLOGY, 2019, 37 (15)
  • [39] Abiraterone acetate followed by enzalutamide in chemotherapy-naive metastatic castration-resistant prostate cancer (mCRPC) treated in the US Oncology Community Setting.
    Vogelzang, Nicholas J.
    Asmar, Lina
    Tang, Jun
    Yap, Mark
    Todd, Mary Beth
    Ng, Yvette
    Mehra, Maneesha
    Patt, Debra A.
    JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (15)
  • [40] Hospitalization costs among chemotherapy-naive metastatic castration-resistant prostate cancer (mCRPC) patients newly treated with enzalutamide (ENZA) or abiraterone (ABI)
    Ramaswamy, Krishnan
    Gilligan, Adrienne M.
    Lenhart, Gregory
    Flanders, Scott
    Schultz, Neil M.
    Mardekian, Jack
    Kent, Shia T.
    JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (15)