Evidence map›Paper›PMID 40596855›Full record

ArticleBMC gastroenterology2025

Feasibility, efficacy, and safety of ventral caudal artery access for transarterial chemoembolization in a rat hepatocellular carcinoma model.

Wei Hong, Zizhuo Wang, Lijie Zhang, Xin Zhang, Wei Yao, Tingting Yang, Chuansheng Zheng, Fengyong Liu, Bin Liang

Abstract read
In one paragraph

Article in BMC gastroenterology, 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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0cells of the map it votes in
0citing papers in PubMed
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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

9 authors.

Wei Hong *Department of Radiology, Hubei Key Laboratory of Molecular Imaging, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1277 Jiefang Road, Wuhan, 430022, China.
Zizhuo Wang *Department of Radiology, Hubei Key Laboratory of Molecular Imaging, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1277 Jiefang Road, Wuhan, 430022, China.
Lijie ZhangDepartment of Radiology, Hubei Key Laboratory of Molecular Imaging, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1277 Jiefang Road, Wuhan, 430022, China.
Xin ZhangDepartment of Radiology, Hubei Key Laboratory of Molecular Imaging, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1277 Jiefang Road, Wuhan, 430022, China.
Wei YaoDepartment of Radiology, Hubei Key Laboratory of Molecular Imaging, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1277 Jiefang Road, Wuhan, 430022, China.
Tingting YangDepartment of Radiology, Hubei Key Laboratory of Molecular Imaging, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1277 Jiefang Road, Wuhan, 430022, China.
Chuansheng ZhengDepartment of Radiology, Hubei Key Laboratory of Molecular Imaging, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1277 Jiefang Road, Wuhan, 430022, China.
Fengyong LiuDepartment of Interventional Radiology, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, 100039, China.
Bin LiangDepartment of Radiology, Hubei Key Laboratory of Molecular Imaging, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1277 Jiefang Road, Wuhan, 430022, China. bliang@hust.edu.cn.

Funding

Fundamental Research Funds for the Central Universities YCJJ20242419
6 · The paper itself

Abstract

purposeInvestigate the feasibility, efficacy, and safety of ventral caudal artery (VCA) approach for transarterial chemoembolization (TACE) in an orthotopic hepatocellular carcinoma (HCC) rat model.

methodsSixteen orthotopically established tumor-bearing Sprague-Dawley rats were divided into two groups of eight each: drug-eluting bead transarterial chemoembolization (DEB-TACE) group and normal saline (NS) group. VCA was approached for transarterial procedures. Rats in DEB-TACE group and NS group received transarterial administration of doxorubicin-loaded microspheres and normal saline, respectively. In NS group, repeated transarterial procedures were attempted 3 days after initial procedures. The feasibility was evaluated based on success rate of VCA approach, proper hepatic artery catheterization, and transcatheter treatment. The efficacy was assessed according to tumor necrosis. Animal mortality and tail viability were observed for safety evaluation. In supplementary experiments, eight additional tumor-bearing rats were used to evaluate the repeatability of proper hepatic artery catheterization via VCA access at 14 days after initial transarterial procedures the same as the NS group. The safety during the 14 days was also evaluated.

resultsVCA was successfully approached in 16 rats at initial procedures. Catheterization of proper hepatic artery achieved success in 7 of 8 DEB-TACE group animals and 6 of 8 NS group animals at initial procedures. All 13 rats received subsequent DEB-TACE or NS injection. One animal in DEB-TACE group died within 24 h and no death was noted in NS group (14.29% vs. 0%, P = 1.000). Tail viability was normal within 3 days. Repeated transarterial procedures were successfully performed in 6 of 8 NS group animals. Tumor necrosis of DEB-TACE group was significantly higher than that of NS group (54.11 ± 22.31% vs. 11.15 ± 3.50%, P = 0.005). In supplementary experiments, repeated catheterization of proper hepatic artery via repeated VCA access was achieved in 7 of 8 rats that had undergone successful initial procedures. There was no death noted and the tail viability maintained normal during the 14 days after initial procedures.

conclusionVCA access is feasible, effective, safe for TACE in rat HCC model.

Indexed as

Carcinoma, HepatocellularChemoembolization, TherapeuticLiver NeoplasmsLiver Neoplasms, ExperimentalAnimalsAntibiotics, AntineoplasticDisease Models, AnimalDoxorubicinFeasibility StudiesHepatic ArteryMaleRatsRats, Sprague-DawleyAntibiotics, AntineoplasticDoxorubicinAnimal modelArtery accessHepatocellular carcinomaTransarterial chemoembolizationVentral caudal artery

Identifiers

PMID40596855
PMCPMC12211226

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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.