Evidence map›Paper›PMID 41208968›Full record

ArticleFrontiers in immunology2025

Hepatic arterial infusion chemotherapy combined with lenvatinib and toripalimab for large hepatocellular carcinoma (> 10 cm) with major portal vein tumor thrombosis: a multicenter propensity score matching analysis.

Yangyang Li, Danchen Wang, Fengtao Zhang, Xiang Zheng, Yipei Song, Yang Ran, Xiangran Cai

Abstract readMulticenter Study
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers 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

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Yangyang Li *Department of Radiology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China.
Danchen Wang *Department of Radiology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China.
Fengtao Zhang *Vascular Interventional Surgery, Shenzhen Nanshan People's Hospital, Shenzhen, Guangdong, China.
Xiang ZhengDepartment of Interventional Therapy, Zhuhai People's Hospital(Zhuhai Clinical Medical College of Jinan University), Zhuhai, Guangdong, China.
Yipei SongDepartment of Radiology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China.
Yang RanGuangdong Provincial Key Laboratory of Optical Fiber Sensing and Communications, Institute of Photonics Technology, Jinan University, Guangzhou, Guangdong, China.
Xiangran CaiDepartment of Radiology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Portal vein main trunk tumor thrombus is one of the most intractable complications of hepatocellular carcinoma(HCC), often occurring in patients with high intrahepatic tumor burden(>10 cm). High tumor burden HCC complicated by portal vein main trunk tumor thrombus is regarded as the very advanced stage with extremely poor therapeutic efficacy and very limited treatment options and its long-term survival depends on the dual remission of intra-hepatic tumors and tumor thrombi. Previous phase III trials have confirmed the ability of HAIC to effectively relieve high tumor burden HCC, yet HAIC alone cannot effectively manage tumor thrombi and intrahepatic progression. The efficacy of the combination of HAIC, lenvatinib and toripalimab in advanced HCC has also been confirmed by existing clinical evidence. Therefore, the combination of HAIC, lenvatinib and toripalimab may be a potentially effective treatment regimen for high tumor burden HCC complicated by portal vein main trunk tumor thrombus. Methods: A retrospective review was conducted on the clinical data of patients with high tumor burden HCC complicated by main portal vein tumor thrombus who received HAIC combined with lenvatinib and toripalimab(HAICLT group) or HAIC alone(HAIC group) from August 2019 to December 2023. Propensity score matching was employed to balance the baseline differences between the groups. The overall survival time, progression-free survival time, objective response rate, and disease control rate were compared between the groups. Results: After PSM, the median OS and median PFS of the HAICLT group were 21.2 months and 7.4 months respectively, significantly better than 6.6 months(HR: 0.35; 95% CI: 0.22-0.56, P < 0.001) and 3.0 months(HR: 0.45; 95% CI: 0.31-0.66, P < 0.001) of the HAIC group. In terms of treatment response, the HAICLT group also accomplished higher rates of intrahepatic responses(ORR: 57.7% vs 19.7%, P<0.001; DCR: 91.5% vs 59.2%, P<0.001) and PVTT responses(ORR: 62.0% vs 21.1%, P<0.001; DCR: 93.0% vs 50.7%, P<0.001) compared to the HAIC group. No significant statistical differences were found in the incidence rates of adverse events at all grades and grades 3-4 between the groups. Conclusion: Compared with HAIC alone, the combination of HAIC, lenvatinib, and toripalimab can effectively prolong the survival prognosis of patients with large HCC complicated by major PVTT and achieve intrahepatic and PVTT remission. It is a promising treatment approach.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, HepatocellularLiver NeoplasmsPhenylurea CompoundsPortal VeinQuinolinesVenous ThrombosisAdultAgedAntibodies, Monoclonal, HumanizedFemaleHepatic ArteryHumansInfusions, Intra-ArterialMaleMiddle AgedAntibodies, Monoclonal, HumanizedlenvatinibPhenylurea CompoundsQuinolinestoripalimabhepatic artery infusion chemotherapyhepatocellular carcinomahigh tumor burdenlenvatinibportal vein tumor thrombosispropensity score matchingtoripalimab

Identifiers

PMID41208968
PMCPMC12592185

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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.