Evidence map›Paper›PMID 42582241›Full record

ArticleFrontiers in immunology2026

Efficacy and safety of TACE combined with MWA followed by immune checkpoint inhibitors and anti-VEGF/tyrosine kinase inhibitors in hepatocellular carcinoma beyond the up-to-7.

Yang Fang, Jiangyu Tan, Xiaoting Su, Minghu Sun, Xianchun Zhou, Songnan Zhang

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Article in Frontiers in immunology, 2026. 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

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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.

Yang Fang *Department of Oncology, the Affiliated Hospital of Yanbian University (Yanbian Hospital), Yanji, China.
Jiangyu Tan *Department of Oncology, the Affiliated Hospital of Yanbian University (Yanbian Hospital), Yanji, China.
Xiaoting SuDepartment of Oncology, the Affiliated Hospital of Yanbian University (Yanbian Hospital), Yanji, China.
Minghu SunDepartment of Interventional Radiology Center, the Affiliated Hospital of Yanbian University (Yanbian Hospital), Yanji, China.
Xianchun ZhouDepartment of Oncology, the Affiliated Hospital of Yanbian University (Yanbian Hospital), Yanji, China.
Songnan ZhangDepartment of Oncology, the Affiliated Hospital of Yanbian University (Yanbian Hospital), Yanji, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Previous studies have shown that locoregional therapy combined with systemic treatment provides survival benefits with manageable safety in patients with intermediate-to-advanced large hepatocellular carcinoma (HCC). However, the optimal treatment strategy for HCC beyond the up-to-7 criteria remains unclear because of the high tumor burden and recurrence risk. This study aimed to evaluate the efficacy and safety of transarterial chemoembolization (TACE) plus microwave ablation (MWA) followed by targeted immunotherapy in patients with HCC beyond the up-to-7 criteria. Methods: This single-center retrospective study included patients with HCC beyond the up-to-7 criteria treated at our institution between October 2018 and December 2023. The study group received TACE plus MWA followed by ICIs combined with anti-VEGF/TKI therapy, while the control group received TACE followed by ICIs combined with anti-VEGF/TKI therapy. The primary endpoint was progression-free survival (PFS) assessed by mRECIST, and the secondary endpoints were overall survival (OS) and treatment-related adverse events (TRAEs).Baseline data were balanced using a one-to-one propensity score matching (PSM) and inverse probability of treatment weighting (IPTW). Result: Among the 80 included patients, the median follow-up time was 68.4 months. Thirty patients had hepatitis B and 40 had hepatitis C. Patients were classified as BCLC stage A-C, with a median tumor size of 7.1 cm. The control and study groups included 41 and 39 patients, respectively. The median PFS was 5.7 months(95%CI:3.617-7.716) versus 11.4 months(95%CI:8.741-14.125), and the median OS was 16.5 months(95%CI:10.863-22.071) versus 40.2 months (95%CI:34.302-46.165), respectively (both Conclusion: TACE combined with MWA followed by immune checkpoint inhibitors and anti-VEGF/TKI therapy prolonged progression-free and overall survival in patients with HCC beyond the up-to-7 criteria, with manageable safety.

Indexed as

Carcinoma, HepatocellularChemoembolization, TherapeuticImmune Checkpoint InhibitorsLiver NeoplasmsMicrowavesProtein Kinase InhibitorsAgedCombined Modality TherapyFemaleHumansMaleMiddle AgedRetrospective StudiesTreatment OutcomeVascular Endothelial Growth Factor AImmune Checkpoint InhibitorsProtein Kinase InhibitorsVascular Endothelial Growth Factor Ahepatocellular carcinomamicrowave ablationmRECISTtransarterial chemoembolizationUP-TO-7

Identifiers

PMID42582241
PMCPMC13457286

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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.