Efficacy and Safety of PARP Inhibitor Therapy in Advanced Ovarian Cancer: A Systematic Review and Network Meta-analysis of Randomized Controlled Trials

被引:0
作者
Chen, Juying [1 ]
Wu, Xiaozhe [1 ]
Wang, Hongzhe [2 ]
Lian, Xiaoshan [3 ]
Li, Bing [1 ]
Zhan, Xiangbo [4 ]
机构
[1] Guangzhou Concord Canc Ctr, Dept Pharm, Guangzhou, Peoples R China
[2] Shanghai Jiahui Int Hosp, Dept Oncol, Shanghai, Peoples R China
[3] Shenzhen New Frontier United Family Hosp, Dept Pharm, Shenzhen, Peoples R China
[4] Guangzhou Concord Canc Ctr, Dept Gynecol, Guangzhou, Peoples R China
关键词
PARP hibitors; olaparib; rucaparib; niraparib; veliparib; ovarian cancer; OLAPARIB MAINTENANCE THERAPY; DOUBLE-BLIND; POLYMERASE INHIBITORS; COMBINATION CEDIRANIB; PHASE-II; OUTCOMES; BEVACIZUMAB; CARCINOMA; BRCA1; CHEMOTHERAPY;
D O I
10.2174/1573409920666230907093331
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Aims This study aims to evaluate the efficacy and safety of PARP inhibitor therapy in advanced ovarian cancer and identify the optimal treatment for the survival of patients.Background The diversity of PARP inhibitors makes clinicians confused about the optimal strategy and the most effective BRCAm mutation-based regimen for the survival of patients with advanced ovarian cancer.Objectives The objective of this study is to compare the effects of various PARP inhibitors alone or in combination with other agents in advanced ovarian cancer.Methods PubMed, Embase, Cochrane Library, and Web of Science were searched for relevant studies on PARP inhibitors for ovarian cancer. Bayesian network meta-analysis was performed using Stata 15.0 and R 4.0.4. The primary outcome was the overall PFS, and the secondary outcomes included OS, AE3, DISAE, and TFST.Results Fifteen studies involving 5,788 participants were included. The Bayesian network meta-analysis results showed that olaparibANDAI was the most beneficial in prolonging overall PFS and non-BRCAm PFS, followed by niraparibANDAI. However, for BRCAm patients, olaparibTR might be the most effective, followed by niraparibANDAI. Olaparib was the most effective for the OS of BRCAm patients. AI, olaparibANDAI, and veliparibTR were more likely to induce grade 3 or higher adverse events. AI and olaparibANDAI were more likely to cause DISAE.Conclusion PARP inhibitors are beneficial to the survival of patients with advanced ovarian cancer. The olaparibTR is the most effective for BRCAm patients, whereas olaparibANDAI and niraparibANDAI are preferable for non-BRCAm patients.Other More high-quality studies are desired to investigate the efficacy and safety of PARP inhibitors in patients with other genetic performances.
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页码:736 / 751
页数:16
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