Combining Novel Hormonal Therapies with a Poly (ADP-Ribose) Polymerase Inhibitor for Metastatic Castration-Resistant Prostate Cancer: Emerging Evidence

被引:3
作者
Yang, Jie [1 ,2 ]
Xiong, Xingyu [1 ,2 ]
Zheng, Weitao [1 ,2 ]
Liao, Xinyang [1 ,2 ]
Xu, Hang [1 ,2 ]
Yang, Lu [1 ,2 ]
Wei, Qiang [1 ,2 ]
机构
[1] Sichuan Univ, West China Hosp, Ctr Biomed Big Data, Dept Urol,Inst Urol, Chengdu 610041, Peoples R China
[2] Sichuan Univ, Natl Clin Res Ctr Geriatr, West China Hosp, Chengdu 610041, Peoples R China
关键词
poly (ADP-ribose) polymerase inhibitor; mCRPC; first-line therapy; homologous recombination repair; ABIRATERONE ACETATE; DNA-REPAIR; ENZALUTAMIDE; SURVIVAL; MEN; PREDNISONE;
D O I
10.3390/curroncol30120751
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Preclinical and clinical studies have suggested potential synergies of combining poly (ADP-ribose) polymerase (PARP) inhibitors and novel hormonal therapies (NHT) for patients with metastatic castration-resistant prostate cancer (mCRPC). We systematically searched PubMed, ClinicalTrials.gov and ASCO-GU annual meeting abstracts up to March 2023 to identify potential phase III trials reporting the use of combining PARP inhibitors with NHT in the first-line setting for mCRPC. A total of four phase III trials met the criteria for subsequent review. Emerging data suggested that the radiographic progression-free survival (rPFS) was significantly longer in the PARP inhibitor combined with NHT group versus the placebo plus NHT group for the first-line setting of biomarker-unselected mCRPC patients, especially for patients with homologous recombination repair (HRR) mutation (HRR m), and with the greatest benefit for BRCA1/2 mutation (BRCA1/2 m) populations. Final overall survival (OS) data of the PROpel trial indicated a significant improvement in median OS for mCRPC patients with HRR m and BRCA1/2 m receiving olaparib + abiraterone. Prior taxane-based chemotherapy might not influence the efficacy of the combination. Compared with the current standard-of-care therapies, combining NHT with PARP inhibitors could achieve a significant survival benefit in the first-line setting for mCRPC patients with HRR and BRCA1/2 mutations.
引用
收藏
页码:10311 / 10324
页数:14
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