AI Article Synopsis

  • The study aims to compare and rank targeted therapies and immunotherapies for advanced liver cancer (hepatocellular carcinoma) based on their effectiveness.
  • A systematic review included 29 randomized controlled trials with over 13,000 patients, analyzing treatments against the established drug sorafenib.
  • Results highlighted that combinations like sintilimab plus IBI305, camrelizumab plus rivoceranib, and atezolizumab plus bevacizumab significantly improved overall survival compared to sorafenib, suggesting further development of combined therapies.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10413926PMC
http://dx.doi.org/10.1080/07853890.2023.2242384DOI Listing

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