Comparative Efficacy and safety of new targeted therapies and immunotherapies for metastatic triple negative breast cancer: a network meta-analysis

被引:1
|
作者
Leung, John Hang [1 ]
Tai, Yun-Sheng [2 ]
Wang, Shyh-Yau [3 ]
Tsung-Chin, Ho [1 ]
Yip Fion, Hei-Tung [4 ]
Chan, Agnes L. F. [5 ]
Yu-Chen, Hsu [6 ]
机构
[1] Chia Yi Christian Hosp, Ditmanson Med Fdn, Dept Obstet & Gynecol, Chiayi, Taiwan
[2] China Med Univ, An Nan Hosp, Dept Surg, Tainan, Taiwan
[3] China Med Univ, An Nan Hosp, Dept Radiol, Tainan, Taiwan
[4] China Med Univ Hosp, Clin Trial Res Ctr, Management Off Hlth Data, Taichung, Taiwan
[5] China Med Univ, An Nan Hosp, Dept Pharm, Tainan, Taiwan
[6] Chia Yi Christian Hosp, Ditmanson Med Fdn, Dept Gen Surg, Chiayi, Taiwan
关键词
Targeted therapies and immunotherapies; metastatic triple-negative breast cancer; PARP inhibitors; atezolizumab; sacituzumab; PEMBROLIZUMAB PLUS CHEMOTHERAPY; DOUBLE-BLIND; OPEN-LABEL; PACLITAXEL; OLAPARIB; ATEZOLIZUMAB; MULTICENTER; CARCINOMA; AMERICAN; SURVIVAL;
D O I
10.1080/14740338.2022.2116001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background Several therapies directed at novel targets and also immunotherapies have recently shown promising results in advanced or metastatic TNBC. We aimed to compare the efficacy and safety of these new regimens for advanced or metastatic TNBC (mTNBC). Methods The PubMed, Embase, and Cochrane Library electronic databases were searched for phase III randomized trials. We conducted a network meta-analysis to compare the efficacy and safety of new targeted and immunotherapy regimens. Trial quality was assessed using the GRADE method. The comparative outcomes were progression-free survival, overall survival, and G3-4 adverse drug events (ADEs). Results Thirteen phase III randomized controlled trials were identified in the network meta-analysis. Olaparib significantly improved PFS in comparison with the pembrolizumab plus chemotherapy 1, atezolizumab plus nab-paclitaxel and pembrolizumab regimens. Sacituzumab yielded a significant improvement in OS over immunotherapies, veliparib, and chemotherapy alone, but no significantly superiority over pembrolizumab, olaparib, and talazoparib. The risk of >= grade 3 ADEs associated with olaparib was significantly lower than the risks associated with the other regimens. Conclusion For mTNBC, sacituzumab had a better effect on overall survival, with comparatively high risk of SAE, whereas olaparib improved progression-free survival with a lower risk of SAE, particularly in those patients with BRCA mutations.
引用
收藏
页码:243 / 252
页数:10
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