Overall survival from the phase 2 trial of abiraterone, olaparib, or abiraterone + olaparib in first-line metastatic castration-resistant prostate cancer (mCRPC) with DNA repair defects (BRCAAway).
Abstract
16 Background: The BRCAAway trial evaluated the efficacy of abiraterone (Abi) versus olaparib (Ola) versus their combination as first-line therapy in patients (pts) with mCRPC harboring germline or somatic homologous recombination repair mutations (HRRm). It showed that first-line treatment with the Abi/Ola combination significantly improved progression-free survival (PFS) compared with either agent alone or sequentially in pts with BRCA1/2 or ATM alterations. Here, we report the overall survival (OS) outcomes per arm. Methods: BRCAAway was a multi-center, open-label, randomized, phase 2 trial. Eligible pts had progressive mCRPC with HRRm and no prior exposure to PARPi or Abi. Pts with HRRm in BRCA1/2 and/or ATM alterations were randomized 1:1:1 to Arm 1: abiraterone 1000 mg QD + prednisone 5 mg BID (Abi/pred), Arm 2: olaparib 300 mg BID (Ola), or Arm 3: abiraterone/prednisone + olaparib (Abi/pred + Ola). Pts with noncanonical HRRm received olaparib alone (nonrandomized Arm 4: exploratory). Crossover was permitted in Arms 1 and 2. OS was assessed as a key secondary endpoint. OS was measured from randomization until death, and pts were censored at their last clinical encounter. Median OS and landmark OS rates at 24, 36, and 60 months for each arm were estimated using the Kaplan-Meier method. Hazard ratios (HRs) between the randomized arms were obtained using Cox proportional hazards regression, separately comparing Arm 3 vs 1 and Arm 3 vs 2. Results: As of September 30, 2025 (data cutoff), there were 34/61 deaths in the randomized pts (11/19 Arm 1 pts, 13/21 Arm 2 pts, and 10/21 Arm 3 pts) and 12/17 deaths in exploratory Arm 4 pts. Median follow-up time was 46.2 months (m). Arm 3 had the longest median OS of 68 m (95% CI: 38–not reached [NR]), compared to Arm 1 median of 28 m (95% CI: 13–NR) and HR = 0.39 (95% CI: 0.16–0.93), and compared to Arm 2 median of 37 m (95% CI: 26–NR) and HR = 0.51 (95% CI: 0.22–1.18) (Table 1). Arm 3 also had the highest 24-, 36-, and 60-month landmark OS rates compared to Arms 1 and 2. Median OS for the exploratory Arm 4 was 39 m (95% CI: 21–49). Conclusions: In pts with mCRPC harboring BRCA1/2 or ATM alterations, abiraterone/prednisone + olaparib was well tolerated and resulted in significantly improved OS (median of >5 years) compared to either agent used alone or sequentially. Clinical trial information: NCT03012321 . Treatment Median OS (95% CI) in Months 24-Month OS Rate (95% CI) 36-Month OS Rate (95% CI) 60-Month OS Rate (95% CI) HR (95% CI) for Arm 3 vs Arm 1 and Arm 2 Arm 1: Abi/pred (n=19) 28 (13, NR) 55% (29%, 75%) 41% (18%, 63%) 31% (9.5%, 55%) 0.39 (0.16, 0.93) Arm 2: Ola (n=21) 37 (26, NR) 85% (60%, 95%) 53% (29%, 72%) 42% (21%, 63%) 0.51 (0.22, 1.18) Arm 3: Abi/pred + Ola (n=21) 68 (38, NR) 90% (67%, 98%) 86% (62%, 95%) 55% (30%, 74%) 1 [reference] Arm 4: Exploratory (n=17) 39 (21, 49) 66% (36%, 84%) 51% (24%, 73%) 15% (2.4%, 37%) -
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (18)
Maha H. A. Hussain
Robert H. Lurie Comprehensive Cancer Center, Chicago, IL
Masha Kocherginsky
Northwestern University Feinberg School of Medicine and the Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, Illinois, United States
Channing Judith Paller
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins University School of Medicine, Baltimore, MD
Neeraj Agarwal
Division of Medical Oncology Department of Internal Medicine Huntsman Cancer Institute University of Utah Salt Lake City Utah USA
Latifa A. Bazzi
Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL
Nabil Adra
Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN
Zachery R. Reichert
Division of Hematology/Oncology, University of Michigan, Ann Arbor, MI
Jingsong Zhang
Joel Picus
Washington University in St. Louis, St. Louis, MO
Russell Zelig Szmulewitz
Section of Hematology/Oncology, Department of Medicine, University of Chicago, Chicago, IL
Scott T. Tagawa
Weill Cornell Medical Center, NewYork Presbyterian Hospital, New York, NY
Timothy M. Kuzel
Northwestern University, Chicago, IL
Young E. Whang
The University of North Carolina at Chapel Hill, Chapel Hill, NC
Ryan D. Stephenson
Rutgers Cancer Institute of New Jersey, New Brunswick, NJ
Robert Dreicer
University of Virginia School of Medicine, Charlottesville, VA
Daniel Shevrin
NorthShore University Health System, Evanston, IL
Matthew Rettig
Department of Medical Oncology, University of Southern California, Los Angeles, Los Angeles, CA
Emmanuel S. Antonarakis
Masonic Cancer Center, University of Minnesota