Abiraterone and Increased Survival in Metastatic Prostate Cancer

被引:3605
作者
De Bono, Johann S. [1 ,2 ]
Logothetis, Christopher J. [6 ]
Molina, Arturo [7 ]
Fizazi, Karim [8 ]
North, Scott [10 ]
Chu, Luis
Chi, Kim N. [11 ]
Jones, Robert J. [3 ]
Goodman, Oscar B., Jr. [14 ]
Saad, Fred [15 ]
Staffurth, John N. [4 ]
Mainwaring, Paul [16 ]
Harland, Stephen [17 ]
Flaig, Thomas W. [18 ]
Hutson, Thomas E. [19 ]
Cheng, Tina [12 ]
Patterson, Helen [5 ]
Hainsworth, John D. [20 ]
Ryan, Charles J. [21 ]
Sternberg, Cora N. [22 ,25 ]
Ellard, Susan L. [13 ]
Flechon, Aude [9 ]
Saleh, Mansoor
Scholz, Mark
Efstathiou, Eleni [6 ]
Zivi, Andrea [1 ,2 ]
Bianchini, Diletta [1 ,2 ]
Loriot, Yohann [8 ]
Chieffo, Nicole [7 ]
Thian Kheoh [7 ]
Haqq, Christopher M. [7 ]
Scher, Howard I. [23 ,24 ]
机构
[1] Inst Canc Res, Sutton SM2 5PT, Surrey, England
[2] Royal Marsden Hosp, Sutton SM2 5PT, Surrey, England
[3] Inst Canc Sci, Glasgow, Lanark, Scotland
[4] Cardiff Univ, Velindre Hosp, Cardiff, S Glam, Wales
[5] Univ Cardiff, Velindre Hosp, Cambridge, England
[6] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[7] Ortho Biotech Oncol Res & Dev Unit Cougar Biotech, Los Angeles, CA USA
[8] Inst Gustave Roussy, Villejuif, France
[9] Ctr Leon Berard, F-69373 Lyon, France
[10] Cross Canc Inst, Edmonton, AB T6G 1Z2, Canada
[11] Vancouver Canc Ctr, BC Canc Agcy, Vancouver, BC, Canada
[12] Univ Calgary, Calgary, AB, Canada
[13] Ctr So Interior, BC Canc Agcy, Kelowna, BC, Canada
[14] Nevada Canc Inst, Las Vegas, NV USA
[15] Univ Montreal, Montreal, PQ, Canada
[16] Haematol & Oncol Clin Australasia, Milton, Australia
[17] UCL Canc Inst, London, England
[18] Univ Colorado, Ctr Canc, Aurora, CO USA
[19] Texas Oncol Baylor Charles A Sammons Canc Ctr, Dallas, TX USA
[20] Sarah Cannon Res Inst, Nashville, TN USA
[21] Univ Calif San Francisco, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94143 USA
[22] San Camillo Hosp, Rome, Italy
[23] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[24] Weill Cornell Med Coll, New York, NY USA
[25] Forlanini Hosp, Rome, Italy
基金
英国医学研究理事会;
关键词
ANDROGEN-DEPRIVATION THERAPY; HUMAN CYTOCHROME P450(17-ALPHA); I CLINICAL-TRIAL; HORMONAL-THERAPY; PLUS PREDNISONE; CASTRATION; ACETATE; CYP17; TESTOSTERONE; DOCETAXEL;
D O I
10.1056/NEJMoa1014618
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
BACKGROUND Biosynthesis of extragonadal androgen may contribute to the progression of castration-resistant prostate cancer. We evaluated whether abiraterone acetate, an inhibitor of androgen biosynthesis, prolongs overall survival among patients with metastatic castration-resistant prostate cancer who have received chemotherapy. METHODS We randomly assigned, in a 2: 1 ratio, 1195 patients who had previously received docetaxel to receive 5 mg of prednisone twice daily with either 1000 mg of abiraterone acetate (797 patients) or placebo (398 patients). The primary end point was overall survival. The secondary end points included time to prostate-specific antigen (PSA) progression (elevation in the PSA level according to prespecified criteria), progression-free survival according to radiologic findings based on prespecified criteria, and the PSA response rate. RESULTS After a median follow-up of 12.8 months, overall survival was longer in the abiraterone acetate-prednisone group than in the placebo-prednisone group (14.8 months vs. 10.9 months; hazard ratio, 0.65; 95% confidence interval, 0.54 to 0.77; P<0.001). Data were unblinded at the interim analysis, since these results exceeded the pre-planned criteria for study termination. All secondary end points, including time to PSA progression (10.2 vs. 6.6 months; P<0.001), progression-free survival (5.6 months vs. 3.6 months; P<0.001), and PSA response rate (29% vs. 6%, P<0.001), favored the treatment group. Mineralocorticoid-related adverse events, including fluid retention, hypertension, and hypokalemia, were more frequently reported in the abiraterone acetate-prednisone group than in the placebo-prednisone group. CONCLUSIONS The inhibition of androgen biosynthesis by abiraterone acetate prolonged overall survival among patients with metastatic castration-resistant prostate cancer who previously received chemotherapy. (Funded by Cougar Biotechnology; COU-AA-301 ClinicalTrials.gov number, NCT00638690.)
引用
收藏
页码:1995 / 2005
页数:11
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