Efficacy and Safety of Systemic Therapies for Advanced Hepatocellular Carcinoma: A Network Meta-Analysis of Phase III Trials

被引:19
作者
Cucchetti, Alessandro [1 ]
Piscaglia, Fabio [1 ]
Pinna, Antonio Daniele [1 ]
Djulbegovic, Benjamin [2 ,3 ]
Mazzotti, Federico [1 ]
Bolondi, Luigi [1 ]
机构
[1] Alma Mater Studiorum Univ Bologna, Dept Med & Surg Sci DIMEC, Bologna, Italy
[2] Univ S Florida, Dept Internal Med, Div Evidence Based Med, USF Hlth Program Evidence Based Med & Comparat Ef, Tampa, FL 33612 USA
[3] H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL USA
关键词
Hepatocellular carcinoma; Systemic therapy; Sorafenib; Network meta-analysis; Safety; Survival; SORAFENIB; SEARCH; GROWTH; CANCER; AGENTS;
D O I
10.1159/000481314
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim/Background: After the introduction of sorafenib in the treatment of advanced hepatocellular carcinoma (HCC), different studies tried to evaluate whether other systemic therapies can improve survival. To provide a comprehensive indirect treatment comparison of efficacy and safety of novel drugs, a network meta-analysis (NMA) of phase III randomized controlled trials was performed. Methods: After pertinent literature search up to November 1, 2016, 6 studies were eligible for the analysis including 4,812 individual patients with advanced HCC: 2,454 received sorafenib, 577 received brivanib, 530 received sunitinib, 514 received linifanib, 358 received sorafenib + erlotinib and 379 received placebo. Frequentist NMA was used to compare treatments within a single analytical framework. Results: NMA showed that sorafenib alone, regardless of combination with erlotinib, and linifanib provide a significant survival advantage over placebo (p < 0.05) but without any significant difference between each other. Conversely, all regimens significantly ameliorate progression-free survival versus placebo (p < 0.05). The rank order of efficacy was: sorafenib +/- erlotinib, linifanib, brivanib, sunitinib, and placebo. Sorafenib +/- erlotinib was the regimen with the fewest number of adverse events that required discontinuation of treatment, whereas linifanib and brivanib resulted in the most adverse events. The risk-benefit summary identified one cluster of therapies with a similar balance between efficacy and safety which included sorafenib alone or in combination with erlotinib, having, at the same time, the highest efficacy and safety. Conclusions: Sorafenib remains the best systemic treatment for advanced HCC; linifanib also resulted in survival advantages over placebo but with a lower safety profile. (C) 2017 S. Karger AG, Basel
引用
收藏
页码:337 / 348
页数:12
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