Comparing efficacy of first-line treatment of metastatic castration resistant prostate cancer: a network meta-analysis of randomized controlled trials

被引:3
作者
Liu, Yang [1 ]
Deng, Xianzhong [2 ]
Wen, Zhi [1 ]
Huang, Jing [1 ]
Wang, Chongjian [1 ]
Chen, Caixia [1 ]
Bao, Erhao [1 ]
Wang, Jiahao [1 ]
Yang, Xuesong [1 ]
机构
[1] North Sichuan Med Coll, Affiliated Hosp, Dept Urol, Nanchong, Peoples R China
[2] North Sichuan Med Coll, Chengdu Xinhua Hosp, Dept Urol, Chengdu, Peoples R China
关键词
prostate cancer; castration-resistant prostate cancer; metastatic; PARP; targeted therapy; meta-analysis; PLACEBO PLUS PREDNISONE; DOUBLE-BLIND; ABIRATERONE ACETATE; PHASE-III; SURVIVAL ANALYSIS; OPEN-LABEL; MULTICENTER; MEN; ENZALUTAMIDE; DOCETAXEL;
D O I
10.3389/fphar.2023.1290990
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Metastatic castration-resistant prostate cancer (mCRPC) presents significant treatment selection challenges due to limited therapeutic options. This study aimed to comprehensively assess the efficacy of multiple treatment regimens for mCRPC through a network meta-analysis (NMA) of randomized controlled trials (RCTs).Methods: A systematically comprehensive search for randomized controlled trials (RCTs) was performed in Pubmed, Cochrane Library, Embase, and Web of Science databases. The network meta-analysis was employed to compare the overall survival (OS), progression-free survival (PFS), and radiographic progression-free survival (rPFS) among different interventions at specific time points. This study was prospectively registered with PROSPERO (CRD42023422823).Results: A total of 29 RCTs, involving 12,706 patients and investigating 16 interventions, were included in the analysis. Chempretarget ((capivasertib or cabozantinib) + docetaxel + prednisone)) and PARP (Olaparib or rucaparib) inhibitors emerged as interventions that significantly improved survival outcomes compared to first-line treatment in mCRPC patients. Chempretarget demonstrated superior overall survival starting from the 12th month, while PARP inhibitors showed a clear advantage in progression-free survival within the 3-18 months range. Notably, chempre ((Docetaxel or Cabazitaxel) + prednisone) exhibited favorable performance in radiographic progression-free survival during the 3-18 month period.Conclusion: Our findings underscore the efficacy of chempretarget, PARP inhibitors, and chempre in enhancing survival outcomes for mCRPC patients. Further head-to-head comparisons are warranted to validate these results. These findings carry important implications for treatment decision-making in mCRPC and may guide the development of more effective therapeutic strategies.
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页数:15
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