Olaparib in Patients With Metastatic Prostate Cancer With BRCA1/2 Mutation: Results From the TAPUR Study

被引:12
作者
Yang, Eddy S. [1 ]
Halabi, Susan [2 ]
Rothe, Michael [3 ]
Garrett-Mayer, Elizabeth [3 ]
Mangat, Pam K. [3 ,10 ]
Pisick, Evan [4 ]
Dib, Elie [5 ]
Burgess, Earle F. [6 ]
Zakem, Michael [7 ]
Rohatgi, Nitin [8 ]
Bilen, Mehmet A. [9 ]
O'Lone, Raegan [3 ]
Grantham, Gina N. [3 ]
Schilsky, Richard L. [3 ]
机构
[1] Univ Alabama Birmingham, ONeal Comprehens Canc Ctr, Sch Med, Dept Radiol, Birmingham, AL USA
[2] Duke Univ, Med Ctr, Durham, NC USA
[3] Amer Soc Clin Oncol, Alexandria, VA USA
[4] City Hope Natl Med Ctr, Canc Treatment Ctr Amer Chicago, Zion, IL USA
[5] Michigan Canc Res Consortium, Ypsilanti, MI USA
[6] Atrium Hlth, Levine Canc Inst, Charlotte, NC USA
[7] Metro Hlth Canc Ctr, Wyoming, MI USA
[8] Sutter Med Ctr, Sacramento, CA USA
[9] Emory Univ, Winship Canc Inst, Atlanta, GA USA
[10] Amer Soc Clin Oncol, 2318 Mill Rd,Ste 800, Alexandria, VA 22314 USA
关键词
DNA-REPAIR;
D O I
10.1200/PO.22.00505
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE The TAPUR Study is a phase II basket trial that aims to evaluate activity of approved targeted agents in patients with advanced cancers with potentially actionable genomic variants. Data from a cohort of patients with metastatic castrate-resistant prostate cancer (mCRPC) and BRCA1/2 mutations treated with olaparib are reported.METHODS Eligible patients with measurable mCRPC were matched to treatment according to protocol-specified genomic matching rules. Patients had no remaining standard treatment options, Eastern Cooperative Oncology Group performance status 0-2, and adequate organ function. Simon's two-stage design was used with a primary end point of disease control, defined as objective response or stable disease of at least 16-week duration. Secondary end points include radiographic progression-free survival, overall survival, duration of response, duration of stable disease, and safety.RESULTS Thirty patients with mCRPC with BRCA1/2 mutations were treated with olaparib. The disease control rate was 69% (95% CI, 51 to 81), and the objective response rate was 58% (95% CI, 37 to 77). The median radiographic progression-free survival and the median overall survival were 38.4 (95% CI, 16.3 to 52.1) weeks and 76.4 (95% CI, 49.3 to 106.0) weeks, respectively. Six of 30 (20%) patients experienced grade 3-4 adverse or serious adverse events including anemia, aspiration, decreased WBC count, and fatigue.CONCLUSION Olaparib has antitumor activity in patients with mCRPC with BRCA1/2 mutations and warrants further study to determine how to best integrate it into the standard treatment of patients with BRCA1/2-mutated prostate cancer.
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页数:10
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