Evidence map›Paper›PMID 41777890›Full record

ArticleFrontiers in immunology2026

Retrospective analysis of transarterial chemoembolization or hepatic arterial infusion chemotherapy combined with lenvatinib with or without PD-1 inhibitor as first-line therapy for unresectable hepatocellular carcinoma with high tumor burden: a propensity score-matched study.

Zhenfeng Li, Huiyong Wu, Ran Xu, Xu Chang, Shushan Wang, Peng Sun

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Zhenfeng LiDepartment of Intervention Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong, China.
Huiyong WuDepartment of Intervention Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong, China.
Ran XuDepartment of Medical Imaging Department, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong, China.
Xu ChangDepartment of Medical Imaging Department, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong, China.
Shushan WangDepartment of Intervention Oncology, Tai'an Cancer Hospital, Tai'an, Shandong, China.
Peng SunDepartment of Intervention Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To compare the efficacy, safety, and hepatic impact of TACE or HAIC plus lenvatinib with or without PD-1 inhibitors in unresectable hepatocellular carcinoma with high tumor burden (HTB-uHCC). Patients and methods: This retrospective study (2019-2023) included 278 HTB-uHCC patients (defined as tumors exceeding the up-to-11 criteria or exhibiting Vp4 portal vein tumor thrombus) receiving either doublet therapy (TACE or HAIC + lenvatinib, THL) or triplet therapy (TACE or HAIC + lenvatinib + PD-1 inhibitor, THLP) (139 per cohort after 1:1 propensity score matching; caliper=0.2). Primary endpoints included overall survival (OS) and progression-free survival (PFS). Secondary endpoints comprised objective response rate (ORR), serial liver function tests, and adverse events (AEs). Results: The THLP group demonstrated superior OS (median22.4 vs. 17.6 months, HR = 0.55, P < 0.001), PFS (13.5 vs. 8.5 months, HR = 0.53, P < 0.001), and ORR (72.7% vs. 52.5%, P < 0.001) compared to the THL group. No intergroup differences in albumin-bilirubin (ALBI) scores were observed at baseline or during months 1-5 (all P > 0.05). Both cohorts showed significant ALBI deterioration at progression versus baseline (P < 0.001). Child-Pugh stability at 6 months independently predicted ORR (adjusted OR 8.71, 95% CI 4.93-15.40; P <0.001). Grade 3-4 AEs occurred at comparable rates (46.8%vs. 43.2%,P=0.629), with no treatment-related deaths. Conclusion: Triplet therapy significantly improves survival and tumor response without accelerating early liver function decline in patients with HTB-uHCC. Child-Pugh stability correlates strongly with treatment efficacy.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, HepatocellularChemoembolization, TherapeuticImmune Checkpoint InhibitorsLiver NeoplasmsPhenylurea CompoundsQuinolinesAgedFemaleHepatic ArteryHumansInfusions, Intra-ArterialMaleMiddle AgedPropensity ScoreRetrospective StudiesImmune Checkpoint InhibitorslenvatinibPhenylurea CompoundsQuinolineshepatic arterial infusion chemotherapyhigh tumor burdenlenvatinibliver functionprogrammed death 1 inhibitorstransarterial chemoembolizationunresectable hepatocellular carcinoma

Identifiers

PMID41777890
PMCPMC12950717

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Registered trials

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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.