Abiraterone, Olaparib, or Abiraterone plus Olaparib in First-Line Metastatic Castration-Resistant Prostate Cancer with DNA Repair Defects (BRCAAway)

被引:6
|
作者
Hussain, Maha [1 ]
Kocherginsky, Masha [2 ]
Agarwal, Neeraj [3 ]
Adra, Nabil [4 ]
Zhang, Jingsong [5 ]
Paller, Channing J. [6 ]
Picus, Joel [7 ]
Reichert, Zachery R. [8 ]
Szmulewitz, Russell Z. [9 ]
Tagawa, Scott T. [10 ]
Kuzel, Timothy M. [1 ]
Bazzi, Latifa A. [2 ]
Daignault-Newton, Stephanie [11 ]
Whang, Young E. [12 ]
Dreicer, Robert [13 ]
Stephenson, Ryan D. [14 ]
Rettig, Matthew B. [15 ]
Shevrin, Daniel [16 ]
Gerke, Travis [17 ]
Chinnaiyan, Arul M. [18 ]
Antonarakis, Emmanuel S. [19 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Div Hematol Oncol, Dept Med, Chicago, IL USA
[2] Northwestern Univ, Feinberg Sch Med, Dept Prevent Med, Div Biostat, Chicago, IL USA
[3] Huntsman Canc Inst, Med, Salt Lake City, UT USA
[4] Indiana Univ Sch Med, Hematol Oncol, Indianapolis, IN USA
[5] H Lee Moffitt Canc Ctr & Res Inst, Dept Genitourinary Oncol, Tampa, FL USA
[6] Johns Hopkins Univ, Oncol, Baltimore, MD USA
[7] Washington Univ, St Louis Sch Med, Med, St. Louis, MO USA
[8] Univ Michigan, Div Hematol Oncol, Ann Arbor, MI USA
[9] Univ Chicago, Dept Med, Chicago, IL USA
[10] Weill Cornell Med, Dept Med, New York, NY USA
[11] Univ Michigan, Urol, Ann Arbor, MI USA
[12] Univ North Carolina Chapel Hill, Med Oncol, Chapel Hill, NC USA
[13] Univ Virginia, Med, Charlottesville, VA USA
[14] Rutgers Canc Inst New Jersey, New Brunswick, NJ USA
[15] Univ Calif Los Angeles, Sch Med, Dept Urol, Los Angeles, CA USA
[16] Northshore Univ Hlth Syst, Dept Cardiovasc Med, Evanston, IL USA
[17] Prostate Canc Clin Trials Consortium, New York, NY USA
[18] Univ Michigan, Pathol, Ann Arbor, MI USA
[19] Univ Minnesota, Masonic Canc Ctr, Minneapolis, MN USA
关键词
INCREASED SURVIVAL; POLYMERASE; ENZALUTAMIDE; PREDNISONE; ACETATE; TUMORS; ROLES; MEN;
D O I
10.1158/1078-0432.CCR-24-1402
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Deleterious germline/somatic homologous recombination repair mutations (HRRm) are present in similar to 25% of patients with metastatic castration-resistant prostate cancer (mCRPC). Preclinically, poly(ADP-ribose) polymerase (PARP) inhibition demonstrated synergism with androgen receptor pathway (ARP)-targeted therapy. This trial evaluated the efficacy of ARP inhibitor versus PARP inhibitor versus their combination as first-line therapy in patients with mCRPC with HRRms.Patients and Methods: BRCAAway is a biomarker preselected, randomized, phase 2 trial. Patients with BRCA1/2 and/or ATM alterations were randomized 1:1:1 to Arm1: abiraterone (1,000 mg)/prednisone (5 mg BID) (Abi/pred), Arm2: olaparib (300 mg BID) (Ola), or Arm3: abiraterone/prednisone + olaparib (Abi/pred + Ola). Single-agent arms could cross over at progression. Exploratory Arm4 patients with other HRRms received olaparib alone. The primary endpoint was progression-free survival (PFS), and secondary endpoints were objective response, PSA response, and safety.Results: Sixty-one of 165 eligible patients had BRCA1/2 or ATM mutations: median age: 67 (IQR, 62-73) years. Mutations: BRCA1 n = 3, BRCA2 n = 46, ATM n = 11, and multiple n = 1; 33 germline and 28 somatic mutations. Median PFS [95% confidence interval (CI)]: Abi/pred, 8.6 months (m; 2.9, 17), Ola, 14 m (8.4, 20), and Abi/pred + Ola, 39 m [22, not reached (NR)]. There were no G4/5 adverse events; 8/19 patients on Abi/pred treatment crossed over to Ola, and 8/21 vice versa. Median PFS (95% CI) from crossover: Ola-after-Abi/pred, 8.3 m (5.5, 15) and Abi/pred-after-Ola, 7.2 m (2.8, NR). Median PFS (95% CI) from randomization: Ola-after-Abi/pred, 16 m (7.8, 25) and Abi/pred-after-Ola, 16 m (11, NR). Seventeen of 165 patients with other HRRms received olaparib: median PFS (95% CI): 5.5 m (2, 11).Conclusions: In patients with mCRPC with BRCA1/2 or ATM HRRm, Abi/pred + Ola was well tolerated and demonstrated longer PFS versus either agent alone or sequentially.
引用
收藏
页码:4318 / 4328
页数:11
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