Five-year Survival Prediction and Safety Outcomes with Enzalutamide in Men with Chemotherapy-naive Metastatic Castration-resistant Prostate Cancer from the PREVAIL Trial

被引:107
作者
Armstrong, Andrew J. [1 ]
Lin, Ping [2 ]
Tombal, Bertrand [3 ]
Saad, Fred [4 ]
Higano, Celestia S. [5 ,6 ]
Joshua, Anthony M. [7 ,12 ]
Parli, Teresa [8 ]
Rosbrook, Brad [9 ]
van Os, Steve [10 ]
Beer, Tomasz M. [11 ]
机构
[1] Duke Univ, Div Med Oncol & Urol, Duke Canc Inst, DUMC Box 103861, Durham, NC 27710 USA
[2] Biostat Pfizer Inc, San Francisco, CA USA
[3] Clin Univ St Luc, Urol, Brussels, Belgium
[4] Ctr Hosp Univ Montreal, Div Urol & Urol Oncol, Montreal, PQ, Canada
[5] Univ Washington, Med Oncol, Seattle, WA 98195 USA
[6] Fred Hutchinson Canc Res Ctr, 1124 Columbia St, Seattle, WA 98104 USA
[7] St Vincents Hosp, Kinghorn Canc Ctr, Dept Med Oncol, Sydney, NSW, Australia
[8] Pfizer Inc, Clin Dev, San Francisco, CA USA
[9] Pfizer Inc, Biostat, San Diego, CA USA
[10] Astellas Pharma Europe BV, Biostat, Leiden, Netherlands
[11] Oregon Hlth & Sci Univ, Hematol Med Oncol, OHSU Knight Canc Inst, Portland, OR 97201 USA
[12] Princess Margaret Canc Ctr, Dept Med Oncol, Toronto, ON, Canada
关键词
Enzalutamide; Metastatic castration-resistant prostate cancer; Multivariable model; Overall survival; Prostate-specific antigen; Safety; ANTIGEN; ABIRATERONE; SURROGACY; THERAPY;
D O I
10.1016/j.eururo.2020.04.061
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: In the PREVAIL study, enzalutamide significantly improved clinical outcomes versus placebo in patients with chemotherapy-naive metastatic castration-resistant prostate cancer (mCRPC). Objective: To evaluate long-term benefits and risks of enzalutamide in the final prespecified PREVAIL analysis. Design, setting, and participants: We conducted a final 5-yr survival analysis of PREVAIL in men with chemotherapy-naive mCRPC from the enzalutamide (n = 689) and placebo (n = 693) arms. Outcome measurements and statistical analysis: Predictors of the primary outcome of overall survival were estimated using the Kaplan-Meier method. Long-term adverse events over time were analyzed. Results and limitations: At the 5-yr data cutoff, 1382 of 1717 (80%) men had died. Enzalutamide reduced the hazard of death by 17% (hazard ratio 0.83; 95% confidence interval [CI] 0.75-0.93; p < 0.001), despite 65%, 54%, and 43% of placebo-treated patients receiving subsequent docetaxel, abiraterone, and enzalutamide, respectively. Median overall survival was 36 mo (95% CI 34-38) in the enzalutamide arm versus 31 mo (95% CI 29-34) in the placebo arm, with a median follow-up of 69 mo. Prognostic modeling showed 5-yr survival rates of 42%, 24%, and 5% for low-, intermediate-, and high-risk groups, respectively. Greater degrees of confirmed prostate-specific antigen declines (<= 3 mo) were associated with greater 5-yr survival. A higher incidence of fatal treatment-emergent adverse events was observed with enzalutamide (6.9% vs 3.8%), with an increase in fatal cardiovascular events (1.6% vs 0.4%). Conclusions: With >5 yr of follow-up, enzalutamide continued to demonstrate improved survival in patients with mCRPC despite crossover and multiple subsequent effective therapies, balanced against a slightly higher rate of fatal cardiovascular events. PREVAIL is registered on ClinicalTrials.gov as NCT01212991. Patient summary: We report a maintained long-term survival benefit with enzalutamide and risks with >5 yr of enzalutamide treatment and follow-up in men with metastatic prostate cancer, and identify groups of men with widely different outcomes based on clinical factors. (C) 2020 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:347 / 357
页数:11
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