Evidence map›Paper›PMID 41782861›Full record

ArticleFrontiers in immunology2026

Hepatic arterial infusion chemotherapy combined with apatinib plus camrelizumab for advanced hepatocellular carcinoma with type Vp4 portal vein tumor thrombosis: a multicenter propensity score-matching analysis.

Shaoteng Wu, Feifeng Qiu, Fengtao Zhang, Pingkang Chen, Xiang Zheng, Qiming Wei, Haiming Zhang, Cheng Qian, Ankang Shu, Ming Li and 2 more

Abstract readMulticenter Study
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. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. Review
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

12 authors.

Shaoteng Wu *Department of Tumor and Vascellum Intervention, DongGuan Tungwah Hospital, DongGuan, Guangdong, China.
Feifeng Qiu *Department of Interventional Surgery Room, The First Affiliated Hospital of Jinan University, Guangzhou, China.
Fengtao Zhang *Vascular Interventional Surgery, Shenzhen Nanshan People's Hospital (Affiliated Nanshan Hospital of Shenzhen University), Shenzhen, Guangdong, China.
Pingkang ChenDepartment of Interventional Therapy, Zhuhai People's Hospital (Zhuhai Clinical Medical College of Jinan University), Zhuhai, Guangdong, China.
Xiang ZhengDepartment of Interventional Therapy, Zhuhai People's Hospital (Zhuhai Clinical Medical College of Jinan University), Zhuhai, Guangdong, China.
Qiming WeiDepartment of Interventional, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
Haiming ZhangDepartment of Radiology, the First Affiliated Hospital of Guangdong Pharmaceutical University, Guangzhou, Guangdong, China.
Cheng QianSchool of Science and Engineering, The Chinese University of Hong Kong Shenzhen, Shenzhen, Guangdong, China.
Ankang ShuDepartment of Tumor and Vascellum Intervention, DongGuan Tungwah Hospital, DongGuan, Guangdong, China.
Ming LiDepartment of Tumor and Vascellum Intervention, DongGuan Tungwah Hospital, DongGuan, Guangdong, China.
Dejun XiongDepartment of Tumor and Vascellum Intervention, DongGuan Tungwah Hospital, DongGuan, Guangdong, China.
Sheng ZhongDepartment of Tumor and Vascellum Intervention, DongGuan Tungwah Hospital, DongGuan, Guangdong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Portal vein main trunk invasion is a serious and difficult complication of hepatocellular carcinoma (HCC), with extremely poor prognosis and limited treatment options. The traditional standard sorafenib has a limited efficacy. The combination of hepatic arterial infusion chemotherapy (HAIC) with camrelizumab and apatinib has shown satisfactory efficacy in previously advanced HCC. Therefore, this approach has potential advantageous survival benefits for HCC with invasion of the portal vein main trunk. Methods: A retrospective review was conducted on the clinical data of advanced HCC patients with type Vp4 portal vein invasion who received HAIC combined with apatinib and camrelizumab (HAICAC group) or HAIC alone (HAIC group) treatment in four medical centers from June 2016 to December 2023. Propensity score matching was employed to balance the baseline differences between the groups. The overall survival, progression-free survival, objective response rate and disease control rate were compared between the groups. Results: Following PSM, the HAICAC regimen demonstrated significantly superior clinical outcomes, with median OS (24.1 versus 7.2 months) and PFS (7.0 versus 4.3 months) significantly exceeding those of HAIC monotherapy (all P<0.001). The combination therapy also exhibited markedly improved tumor response rates, achieving superior objective response rates for both intrahepatic lesions (75.6% versus 31.4%, P<0.001) and PVTT (60.5% versus 17.4%, P<0.001). While the HAICAC group showed a higher incidence of immune-related adverse events compared to the HAIC group, all events were manageable and no grade 5 toxicities occurred. Conclusion: For HCC with Vp4 type PVTT, the combination regimen of HAIC plus apatinib and camrelizumab demonstrates promising efficacy in reducing both intrahepatic tumor burden and thrombus progression, representing a potentially viable treatment approach with an acceptable safety profile.

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, HepatocellularLiver NeoplasmsPortal VeinPyridinesVenous ThrombosisAgedFemaleHepatic ArteryHumansInfusions, Intra-ArterialMaleMiddle AgedPropensity ScoreRetrospective StudiesAntibodies, Monoclonal, HumanizedapatinibcamrelizumabPyridinesapatinibcamrelizumabhepatic arterial infusion chemotherapyhepatocellular carcinomaportal vein main trunk invasion

Identifiers

PMID41782861
PMCPMC12953477

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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.