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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  • [21] Beyond DNA repair, the immunological role of PARP-1 and its siblings
    Rosado, Maria Manuela
    Bennici, Elisabetta
    Novelli, Flavia
    Pioli, Claudio
    [J]. IMMUNOLOGY, 2013, 139 (04) : 428 - 437
  • [22] PROpel: Phase III trial of olaparib (ola) and abiraterone (abi) versus placebo (pbo) and abi as first-line (1L) therapy for patients (pts) with metastatic castration-resistant prostate cancer (mCRPC).
    Saad, Fred
    Armstrong, Andrew J.
    Thiery-Vuillemin, Antoine
    Oya, Mototsugu
    Loredo, Eugenia
    Procopio, Giuseppe
    de Menezes, Juliana Janoski
    Girotto, Gustavo Colagiovanni
    Arslan, Cagatay
    Mehra, Niven
    Parnis, Francis
    Brown, Emma
    Schluermann, Friederike
    Joung, Jae Young
    Sugimoto, Mikio
    Poehlein, Christian Heinrich
    Harrington, Elizabeth
    Desai, Chintu
    Kang, Jinyu
    Clarke, Noel
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2022, 40 (06)
  • [23] PARPi Triggers the STING-Dependent Immune Response and Enhances the Therapeutic Efficacy of Immune Checkpoint Blockade Independent of BRCAness
    Shen, Jianfeng
    Zhao, Wei
    Ju, Zhenlin
    Wang, Lulu
    Peng, Yang
    Labrie, Marilyne
    Yap, Timothy A.
    Mills, Gordon B.
    Peng, Guang
    [J]. CANCER RESEARCH, 2019, 79 (02) : 311 - 319
  • [24] STING-Dependent Cytosolic DNA Sensing Mediates Innate Immune Recognition of Immunogenic Tumors
    Woo, Seng-Ryong
    Fuertes, Mercedes B.
    Corrales, Leticia
    Spranger, Stefani
    Furdyna, Michael J.
    Leung, Michael Y. K.
    Duggan, Ryan
    Wang, Ying
    Barber, Glen N.
    Fitzgerald, Katherine A.
    Alegre, Maria-Luisa
    Gajewski, Thomas F.
    [J]. IMMUNITY, 2014, 41 (05) : 830 - 842
  • [25] Biomarker analysis of phase (Ph) IB trial of radium-223 (Rad) and niraparib (Nira) in patients (Pts) with metastatic castrate-resistant prostate cancer (mCRPC) (NiraRad).
    Yang, Eddy Shih-Hsin
    Leiby, Benjamin
    Sonpavde, Guru P.
    Einstein, David Johnson
    Quinn, Zachary L.
    Szmulewitz, Russell Zelig
    Sartor, A. Oliver
    Kelly, William Kevin
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2021, 39 (15)