Does Gleason score at initial diagnosis predict efficacy of abiraterone acetate therapy in patients with metastatic castration-resistant prostate cancer? An analysis of abiraterone acetate phase III trials

被引:38
作者
Fizazi, K. [1 ]
Flaig, T. W. [2 ]
Stoeckle, M. [3 ]
Scher, H. I. [4 ,5 ]
de Bono, J. S. [6 ,7 ]
Rathkopf, D. E. [4 ,5 ]
Ryan, C. J. [8 ]
Kheoh, T. [9 ]
Li, J. [10 ]
Todd, M. B. [11 ]
Griffin, T. W. [12 ]
Molina, A. [13 ]
Ohlmann, C. H. [3 ]
机构
[1] Univ Paris Sud, Inst Gustave Roussy, Villejuif, France
[2] Univ Colorado, Sch Med, Ctr Canc, Aurora, CO USA
[3] Univ Saarland, Homburg, Germany
[4] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10021 USA
[5] Weill Cornell Med Coll, New York, NY USA
[6] Inst Canc Res, Sutton, Surrey, England
[7] Royal Marsden Hosp, Sutton, Surrey, England
[8] Univ Calif San Francisco, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94143 USA
[9] Janssen Res & Dev, San Diego, CA USA
[10] Janssen Res & Dev, Raritan, NJ USA
[11] Janssen Global Serv, Raritan, NJ USA
[12] Janssen Res & Dev, Los Angeles, CA USA
[13] Janssen Res & Dev, Menlo Pk, CA USA
关键词
abiraterone acetate; chemotherapy-naive; Gleason score; post-chemotherapy; prostate cancer; PLACEBO-CONTROLLED PHASE-3; 2005; INTERNATIONAL-SOCIETY; DOUBLE-BLIND; SURVIVAL ANALYSIS; PROGNOSTIC MODEL; GRADING SYSTEM; CHEMOTHERAPY; MEN; SAFETY; OLDER;
D O I
10.1093/annonc/mdv545
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In this retrospective study of two large phase III studies of patients with metastatic castration-resistant prostate cancer, abiraterone acetate conferred benefit to patients regardless of Gleason score (< 8 versus a parts per thousand yen8) at initial diagnosis.The usefulness of Gleason score (< 8 or a parts per thousand yen8) at initial diagnosis as a predictive marker of response to abiraterone acetate (AA) plus prednisone in patients with metastatic castration-resistant prostate cancer (mCRPC) was explored retrospectively. Initial diagnosis Gleason score was obtained in 1048 of 1195 (COU-AA-301, post-docetaxel) and 996 of 1088 (COU-AA-302, chemotherapy-na < ve) patients treated with AA 1 g plus prednisone 5 mg twice daily by mouth or placebo plus prednisone. Efficacy end points included radiographic progression-free survival (rPFS) and overall survival (OS). Distributions and medians were estimated by Kaplan-Meier method and hazard ratio (HR) and 95% confidence interval (CI) by Cox model. Baseline characteristics were similar across studies and treatment groups. Regardless of Gleason score, AA treatment significantly improved rPFS in post-docetaxel [Gleason score < 8: median, 6.4 versus 5.5 months (HR = 0.70; 95% CI 0.56-0.86), P = 0.0009 and Gleason score a parts per thousand yen8: median, 5.6 versus 2.9 months (HR = 0.58; 95% CI 0.48-0.72), P < 0.0001] and chemotherapy-na < ve patients [Gleason score < 8: median, 16.5 versus 8.2 months (HR = 0.50; 95% CI 0.40-0.62), P < 0.0001 and Gleason score a parts per thousand yen8: median, 13.8 versus 8.2 months (HR = 0.61; 95% CI 0.49-0.76), P < 0.0001]. Clinical benefit of AA treatment was also observed for OS, prostate-specific antigen (PSA) response, objective response and time to PSA progression across studies and Gleason score subgroups. OS and rPFS trends demonstrate AA treatment benefit in patients with pre- or post-chemotherapy mCRPC regardless of Gleason score at initial diagnosis. The initial diagnostic Gleason score in patients with mCRPC should not be considered in the decision to treat with AA, as tumour metastases may no longer reflect the histology at the time of diagnosis. COU-AA-301 (NCT00638690); COU-AA-302 (NCT00887198).
引用
收藏
页码:699 / 705
页数:7
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