Efficacy and safety of second-line therapies for advanced hepatocellular carcinoma: a network meta-analysis of randomized controlled trials

被引:1
|
作者
Lu, Fenping [1 ,2 ]
Zhao, Kai [3 ]
Ye, Miaoqing [4 ]
Xing, Guangyan [1 ,2 ]
Liu, Bowen [1 ,2 ]
Li, Xiaobin [1 ,2 ]
Ran, Yun [2 ]
Wu, Fenfang [2 ]
Chen, Wei [5 ]
Hu, Shiping [2 ]
机构
[1] Beijing Univ Chinese Med, Beijing, Peoples R China
[2] Beijing Univ Chinese Med, Affiliated Shenzhen Hosp, Shenzhen, Peoples R China
[3] Shaanxi Shuangbo Hosp Tradit Chinese Med Liver & K, Xian, Peoples R China
[4] Shaanxi Prov Hosp Tradit Chinese Med, Xian, Peoples R China
[5] Emergency Gen Hosp, Dept Pharm, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Hepatocellular carcinoma; Second-line; Network meta-analysis; Efficacy; Safety; DOUBLE-BLIND; SORAFENIB; PLACEBO; MULTICENTER;
D O I
10.1186/s12885-024-12780-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundThe selection of appropriate second-line therapy for liver cancer after first-line treatment failure poses a significant clinical challenge due to the lack of direct comparative studies and standard treatment protocols. A network meta-analysis (NMA) provides a robust method to systematically evaluate the clinical outcomes and adverse effects of various second-line treatments for hepatocellular carcinoma (HCC).MethodsWe systematically searched PubMed, Embase, Web of Science and the Cochrane Library to identify phase III/IV randomized controlled trials (RCTs) published up to March 11, 2024. The outcomes extracted were median overall survival (OS), median progression-free survival (PFS), time to disease progression (TTP), disease control rate (DCR), objective response rate (ORR), and adverse reactions. This study was registered in the Prospective Register of Systematic Reviews (CRD42023427843) to ensure transparency, novelty, and reliability.ResultsWe included 16 RCTs involving 7,005 patients and 10 second-line treatments. For advanced HCC patients, regorafenib (HR = 0.62, 95%CI: 0.53-0.73) and cabozantinib (HR = 0.74, 95%CI: 0.63-0.85) provided the best OS benefits compared to placebo. Cabozantinib (HR = 0.42, 95%CI: 0.32-0.55) and regorafenib (HR = 0.46, 95% CI: 0.31-0.68) also offered the most significant PFS benefits. For TTP, apatinib (HR = 0.43, 95% CI: 0.33-0.57), ramucirumab (HR = 0.44, 95% CI: 0.34-0.57), and regorafenib (HR = 0.44, 95% CI: 0.38-0.51) showed significant benefits over placebo. Regarding ORR, ramucirumab (OR = 9.90, 95% CI: 3.40-42.98) and S-1 (OR = 8.68, 95% CI: 1.4-154.68) showed the most significant increases over placebo. Apatinib (OR = 3.88, 95% CI: 2.48-6.10) and cabozantinib (OR = 3.53, 95% CI: 2.54-4.90) provided the best DCR benefits compared to placebo. Tivantinib showed the most significant advantages in terms of three different safety outcome measures.ConclusionsOur findings suggest that, in terms of overall efficacy and safety, regorafenib and cabozantinib are the optimal second-line treatment options for patients with advanced HCC.
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页数:13
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