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Protocol published for network meta-analysis of first-line treatments in advanced hepatocellular carcinoma

Protocol published for network meta-analysis of first-line treatments in advanced hepatocellular car…
Photo by Dmytro Vynohradov / Unsplash
Key Takeaway
Note: This is a study protocol; no results or clinical conclusions are available.

Researchers have published a protocol for an individual patient data network meta-analysis that will compare all first-line treatment regimens for advanced hepatocellular carcinoma. The study will include patients with advanced HCC, though the specific sample size, setting, and follow-up duration are not yet reported. The protocol describes plans to compare active first-line treatments against each other.

The primary outcomes will be overall survival, grade ≥3 serious adverse events, and the incremental safety-effectiveness ratio. Secondary outcomes include progression-free survival, objective response rate, incidence of all adverse events, and treatment discontinuation due to adverse events. No results, safety data, or tolerability findings are presented in this protocol.

Key limitations include that this is only a study protocol—the analysis has not been conducted, and the literature search is planned to conclude in March 2026. The certainty of evidence for each outcome will be evaluated using the Confidence in Network Meta-Analysis (CINeMA) application. The authors state the eventual findings are expected to inform clinical guidelines and support personalized therapeutic decisions, but no current clinical recommendations can be made from this protocol document.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedMar 2026
View Original Abstract ↓
BackgroundAdvanced hepatocellular carcinoma (HCC) poses a substantial global disease burden. Since the approval of sorafenib in 2007, an increasing number of treatment regimens have demonstrated encouraging survival benefits in first-line treatment of advanced HCC. However, this expansion of therapeutic options has also introduced complexity into clinical decision-making. This study aims to provide high-quality evidence to inform clinical practice by comparing all first-line treatment regimens for advanced HCC.MethodsWe will systematically search PubMed, Embase (Ovid), and the Cochrane Library (Ovid) from January 1, 2007, to March 3, 2026. Supplementary searches will be performed in clinical trial platforms and conference abstracts. All randomized controlled trials (RCTs) and high-quality observational studies (for prior information only) comparing active first-line treatment regimen for advanced HCC will be included. Primary outcomes are overall survival, grade ≥3 serious adverse events, and the incremental safety-effectiveness ratio. Secondary outcomes include progression-free survival, objective response rate, the incidence of all adverse events and treatment discontinuation due to adverse events. The risk of bias of included RCTs will be assessed using the Risk of Bias 2.0 tool, and the certainty of evidence for each outcome will be evaluated with the Confidence in Network Meta-Analysis (CINeMA) application. Study selection, data extraction, and quality assessment will be performed independently by two reviewers, with any disagreements adjudicated by a third reviewer. Individual patient data will be reconstructed from published Kaplan-Meier curves, and treatment effects will be evaluated using restricted mean survival time. Subgroup analyses will be performed based on PD-L1 expression, etiology, Barcelona Clinic Liver Cancer stage, alpha-fetoprotein concentration, macrovascular invasion, and extrahepatic spread. Bayesian network meta-analysis will be performed using R with the gemtc package.DiscussionOur study is expected to inform clinical guidelines and support personalized therapeutic decisions for advanced HCC.Clinical trial registrationhttps://www.crd.york.ac.uk/PROSPERO/view/, identifier CRD420251126975.
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