Article (Scientific journals)
Non-BRCA DNA Damage Repair Gene Alterations and Response to the PARP Inhibitor Rucaparib in Metastatic Castration-Resistant Prostate Cancer: analysis from the phase 2 TRITON2 study.
Abida, Wassim; Campbell, David; Patnaik, Akash et al.
2020In Clinical cancer research : an official journal of the American Association for Cancer Research, 26 (11), p. 2487-2496
Peer reviewed
 

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Abstract :
[en] PURPOSE: Genomic alterations in DNA damage repair (DDR) genes other than BRCA may confer synthetic lethality with PARP inhibition in metastatic castration-resistant prostate cancer (mCRPC). To test this hypothesis, the phase 2 TRITON2 study of rucaparib included patients with mCRPC and deleterious non-BRCA DDR gene alterations. PATIENTS AND METHODS: TRITON2 enrolled patients who had progressed on 1 to 2 lines of next-generation androgen receptor (AR)-directed therapy and 1 taxane-based chemotherapy for mCRPC. Key endpoints were investigator-assessed radiographic response per modified RECIST/PCWG3 and prostate-specific antigen (PSA) response (>/=50% decrease from baseline). RESULTS: TRITON2 enrolled 78 patients with a non-BRCA DDR gene alteration (ATM [n = 49], CDK12 [n = 15], CHEK2 [n = 12], and other DDR genes [n = 14]). Among patients evaluable for each endpoint, radiographic and PSA responses were observed in a limited number of patients with an alteration in ATM (2/19 [10.5%] and 2/49 [4.1%], respectively), CDK12 (0/10 [0%] and 1/15 [6.7%], respectively), or CHEK2 (1/9 [11.1%] and 2/12 [16.7%], respectively), including no radiographic or PSA responses in 11 patients with confirmed biallelic ATM loss or 11 patients with ATM germline mutations. Responses were observed in patients with alterations in the DDR genes PALB2, FANCA, BRIP1, and RAD51B. Conclusions: In this prospective, genomics-driven study of rucaparib in mCRPC, we found limited radiographic/PSA responses to PARP inhibition in men with alterations in ATM, CDK12, or CHEK2 However, patients with alterations in other DDR-associated genes (eg, PALB2) may benefit from PARP inhibition.
Disciplines :
Oncology
Author, co-author :
Abida, Wassim
Campbell, David
Patnaik, Akash
Shapiro, Jeremy D.
Sautois, Brieuc  ;  Université de Liège - ULiège > Département des sciences cliniques > Département des sciences cliniques
Vogelzang, Nicholas J.
Voog, Eric G.
Bryce, Alan H.
McDermott, Ray
Ricci, Francesco
Rowe, Julie
Zhang, Jingsong
Piulats, Josep Maria
Fizazi, Karim
Merseburger, Axel S.
Higano, Celestia S.
Krieger, Laurence E.
Ryan, Charles J.
Feng, Felix Y.
Simmons, Andrew D.
Loehr, Andrea
Despain, Darrin
Dowson, Melanie
Green, Foad
Watkins, Simon P.
Golsorkhi, Tony
Chowdhury, Simon
More authors (17 more) Less
Language :
English
Title :
Non-BRCA DNA Damage Repair Gene Alterations and Response to the PARP Inhibitor Rucaparib in Metastatic Castration-Resistant Prostate Cancer: analysis from the phase 2 TRITON2 study.
Publication date :
2020
Journal title :
Clinical cancer research : an official journal of the American Association for Cancer Research
ISSN :
1078-0432
Volume :
26
Issue :
11
Pages :
2487-2496
Peer reviewed :
Peer reviewed
Commentary :
Copyright (c)2020, American Association for Cancer Research.
Available on ORBi :
since 11 March 2020

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