Evidence map›Paper›PMID 41436995›Full record

SynthesisBMC cancer2025

The effectiveness and safety of immune checkpoint inhibitors in conversion or neoadjuvant therapy for hepatocellular carcinoma: a meta-analysis and systematic review.

Lingbo Hu, Yongfu Xu, Yingli Qiao, Aidong Wang, Caidi He, Rongrong Wang

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in BMC cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Lingbo HuDepartment of Hepatopancreatobiliary Surgery, Taizhou Hospital of Zhejiang Province affiliated to Wenzhou Medical University, Zhejiang, China.
Yongfu XuDepartment of Hepatopancreatobiliary Surgery, Taizhou Hospital of Zhejiang Province affiliated to Wenzhou Medical University, Zhejiang, China.
Yingli QiaoDepartment of Hepatopancreatobiliary Surgery, Taizhou Hospital of Zhejiang Province affiliated to Wenzhou Medical University, Zhejiang, China.
Aidong WangDepartment of Hepatopancreatobiliary Surgery, Taizhou Hospital of Zhejiang Province affiliated to Wenzhou Medical University, Zhejiang, China.
Caidi HeNursing Department, Taizhou Municipal Hospital (Taizhou University Affiliated Municipal Hospital), School of Medicine, Taizhou University, Zhejiang, China. hcdeye@163.com.
Rongrong WangDepartment of Hepatopancreatobiliary Surgery, Taizhou Hospital of Zhejiang Province affiliated to Wenzhou Medical University, Zhejiang, China. wangrr@enzemed.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe adoption of immune checkpoint inhibitors in combination with tyrosine kinase inhibitors (TKIs) and/or local therapy, including transarterial chemoembolization (TACE) and hepatic arterial infusion chemotherapy (HAIC), has been utilized as neoadjuvant or conversion therapy for hepatocellular carcinoma. However, the efficacy of different combinations in terms of conversion or neoadjuvant therapy varies.

methodsWe conducted a single-group rate meta-analysis to determine the conversion rate or resection rate, tumor response, and corresponding 95% confidence intervals (CI) for the therapeutic combinations. The tumor response and adverse events were also evaluated. The prognosis of patients receiving neoadjuvant therapy followed by surgery and surgery alone was also compared by evaluating HR and its 95%CI.

resultsForty-nine studies were included, with thirty-six studies involving 3497 patients focusing on conversion therapy and the remaining thirteen involving 569 patients focusing on neoadjuvant therapy. The meta-analysis revealed a conversion rate of 0.23 (95% CI: 0.18–0.29). Subgroup analyses based on different treatments revealed a conversion rate of patients receiving is the combination of ICIs, TKIs, and TACE or HAIC about 30%, while the conversion rate of patients receiving T + A is about 4%. When evaluated by modified Response Evaluation Criteria In Solid Tumors (mRECIST), the objective response rate (ORR) is 0.62 (95% CI: 0.56–0.67), the disease control rate is 0.87 (95% CI: 0.84–0.90). The incidence of adverse events (AEs) and severe AEs is 0.95 (95% CI: 0.92–0.98) and 0.39 (95% CI: 0.32–0.46), respectively. The meta-analysis revealed a resection rate of 0.87 (95% CI: 0.85–0.90). The OS and RFS of patients receiving neoadjuvant therapy followed by surgery is similar to those receiving surgery alone.

conclusionOur study provides a comprehensive summary of the current evidence regarding the success rates of conversion therapy, including comparisons between different treatment regimens and associated adverse effects. Additionally, we present findings on the role and side effects of neoadjuvant therapy in resectable HCC.

Indexed as

Carcinoma, HepatocellularImmune Checkpoint InhibitorsLiver NeoplasmsNeoadjuvant TherapyAntineoplastic Combined Chemotherapy ProtocolsChemoembolization, TherapeuticHumansPrognosisTreatment OutcomeImmune Checkpoint InhibitorsConversion therapyHepatocellular carcinomaImmune checkpoint inhibitorsLiver resectionNeoadjuvant therapy

Identifiers

PMID41436995
PMCPMC12859872

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.