Molecular targeted therapy and immunotherapy in advanced hepatocellular carcinoma: a systematic review and Bayesian network meta-analysis based on randomized controlled trials

Ann Med. 2023;55(2):2242384. doi: 10.1080/07853890.2023.2242384.

Abstract

Objective: The aim of this study was to compare and rank different targeted therapies or immunotherapies for advanced hepatocellular carcinoma based on efficacy.

Methods: A systematic search of the PubMed, EMBASE, and Cochrane Library databases was conducted. All systematic treatment regimens that reported comparisons with sorafenib were included in this analysis. The primary outcome measures were overall survival (OS) and progression-free survival (PFS), and other outcome measures included the objective response rate (ORR) and safety analysis according to reported treatment-related adverse events.

Results: A total of 29 RCTs involving 13376 patients were included in the analysis, including 10 single-agent therapies and 17 combination therapies. Compared with sorafenib, sintilimab plus IBI305 (HR: 0.57, 95% CI: 0.43-0.75), camrelizumab plus rivoceranib (HR: 0.62, 95% CI: 0.49-0.78), and atezolizumab plus bevacizumab (HR: 0.66, 95% CI: 0.52-0.83) ranked in the top three in terms of OS.

Conclusions: PD-1/PD-L1 inhibitors combined with anti-vascular endothelial growth factor (anti-VEGF)-targeting drugs have shown better therapeutic effects in the systematic treatment of patients with advanced hepatocellular carcinoma, and the combination of targeted and immune therapy modes should be further developed.

Keywords: Bayesian; Molecular targeted therapy; hepatocellular carcinoma; immunotherapy; meta-analysis.

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't
  • Review
  • Systematic Review

MeSH terms

  • Bayes Theorem
  • Carcinoma, Hepatocellular* / drug therapy
  • Carcinoma, Hepatocellular* / pathology
  • Humans
  • Immunotherapy
  • Liver Neoplasms* / drug therapy
  • Liver Neoplasms* / pathology
  • Molecular Targeted Therapy
  • Network Meta-Analysis
  • Randomized Controlled Trials as Topic
  • Sorafenib / therapeutic use

Substances

  • Sorafenib

Grants and funding

This study was supported in part by grants from the Medical and Health Science and Technology Development Project of Shandong Province (No. 2019WS596), and the Natural Science Foundation of Shandong Province (No. ZR2020MH293).