Differential Response to Olaparib Treatment Among Men with Metastatic Castration-resistant Prostate Cancer Harboring BRCA1 or BRCA2 Versus ATM Mutations

被引:135
作者
Marshall, Catherine H. [1 ]
Sokolova, Alexandra O. [2 ,3 ]
McNatty, Andrea L. [4 ]
Cheng, Heather H. [2 ,3 ]
Eisenberger, Mario A. [1 ]
Bryce, Alan H. [4 ]
Schweizer, Michael T. [2 ,3 ]
Antonarakis, Emmanuel S. [1 ]
机构
[1] Johns Hopkins Sch Med, Sidney Kimmel Comprehens Canc Ctr, 201 North Broadway, Baltimore, MD 21287 USA
[2] Univ Washington, Div Med Oncol, Seattle, WA 98195 USA
[3] Fred Hutch Canc Res Ctr Seattle, Div Clin Res, Washington, DC USA
[4] Mayo Clin, Dept Oncol, Scottsdale, AZ USA
基金
美国国家卫生研究院;
关键词
ATM; BRCA2; Olaparib; PARP inhibitor; Prostate cancer;
D O I
10.1016/j.eururo.2019.02.002
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: Poly ADP-ribose polymerase (PARP) inhibitors, such as olaparib, are being explored as a treatment option for metastatic castration-resistant prostate cancer (mCRPC) in men harboring mutations in homologous recombination DNA-repair genes. Whether responses to PARP inhibitors differ according to the affected gene is currently unknown. Objective: To determine whether responses to PARP inhibitors differ between men with BRCA1/2 and those with ATM mutations. Design, setting, and participants: This was a multicenter retrospective review of 23 consecutive men with mCRPC and pathogenic germline and/or somatic BRCA1/2 or ATM mutations treated with olaparib at three academic sites in the USA. Outcome measurements and statistical analysis: The proportion of patients achieving a >= 50% decline in prostate-specific antigen (PSA(50) response) was compared using Fisher's exact test. Clinical and radiographic progression-free survival (PFS) and overall survival were estimated using Kaplan-Meier analyses and compared using the log-rank test. Results and limitations: The study included two men with BRCA1 mutations, 15 with BRCA2 mutations, and six with ATM mutations. PSA(50) responses to olaparib were achieved in 76% (13/17) of men with BRCA1/2 versus 0% (0/6) of men with ATM mutations (Fisher's exact test; p = 0.002). Patients with BRCA1/2 mutations had median PFS of 12.3 mo versus 2.4 mo for those with ATM mutations (hazard ratio 0.17, 95% confidence interval 0.05-0.57; p = 0.004). Limitations include the retrospective design and relatively small sample size. Conclusions: Men with mCRPC harboring ATM mutations experienced inferior outcomes to PARP inhibitor therapy compared to those harboring BRCA1/2 mutations. Alternative therapies should be explored for patients with ATM mutations. Patient summary: Mutations in BRCA1/2 and ATM genes are common in metastatic prostate cancer. In this study we compared outcomes for men with BRCA1/2 mutations to those for men with ATM mutations being treated with olaparib. We found that men with ATM mutations do not respond as well as men with BRCA1/2 mutations. (C) 2019 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:452 / 458
页数:7
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