ORIGINAL RESEARCH article
Front. Oncol.
Sec. Gastrointestinal Cancers: Hepato Pancreatic Biliary Cancers
This article is part of the Research TopicManagement of Localized Pancreatic CancerView all 3 articles
Efficacy and Safety of Stereotactic Body Radiation Therapy combined with Hepatic Arterial Infusion Chemotherapy for Hepatocellular Carcinoma with Portal Vein Tumor Thrombosis:A Multicenter Propensity Score Matching Study
Provisionally accepted- 1Interventional Surgery, Department of Radiology, Huazhong University of Science and Technology Union Shenzhen Hospital, Shenzhen, China
- 2The First Affiliated Hospital of Jinan University, Guangzhou, China
- 3Zhuhai City People's Hospital, Zhuhai, China
- 4First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China
- 5The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, China
- 6First People's Hospital of Kashi, Kashgar, China
- 7Dongguan Tungwah Hospital, Dongguan, China
- 8The First Affiliated Hospital of Guangdong Pharmaceutical University, Guangzhou, China
Select one of your emails
You have multiple emails registered with Frontiers:
Notify me on publication
Please enter your email address:
If you already have an account, please login
You don't have a Frontiers account ? You can register here
[Abstract] Background: Portal vein tumor thrombosis (PVTT) is among the foremost co-morbidities of hepatocellular carcinoma (HCC), characterized by an inexorably grim prognosis and a paucity of viable therapeutic modalities. Regrettably, the conventional standard sorafenib for HCC patients afflicted with portal vein involvement has yielded suboptimal outcomes. Currently, hepatic arterial infusion chemotherapy (HAIC) and stereotactic body radiation therapy(SBRT) have emerged as promising strategies, particularly in advanced HCC cases complicated by portal vein involvement, showcasing notable survival advantages. Currently, there is no research of HAIC combined with SBRT for HCC patients with PVTT. In this study, we embarked on a multicenter retrospective investigation to elucidate the enhanced survival benefits of this combined modality for HCC patients with portal vein involvement. Methods: Retrospectively collected clinical data from three medical centers in China on patients with HCC and combined PVTT received HAIC combined with SBRT or HAIC alone between September 2019 and June 2022 were analyzed. 1:1 Propensity Score Matching(PSM) was employed to balance baseline differences between the groups. Survival benefits were compared across cohorts using the Kaplan-Meier method, with subgroup analysis conducted to further elucidate outcomes. Univariate and multivariate analyses based on the COX proportional hazards regression model were performed to identify risk factors associated with survival prognosis. Safety was assessed by comparing adverse event rates between the groups. Results: After matching, a total of 146 patients(73 per group) were analyzed. In the matched cohort, the HAIC-SBRT regimen demonstrated significantly superior clinical outcomes compared with HAIC alone. Median overall survival (mOS, 24.5 versus 12.2 months; HR: 0.50, 95% CI: 0.31–0.79; P < 0.001) and median progression-free survival (mPFS, 10.3 versus 6.9 months; HR: 0.67, 95% CI: 0.45–0.99; P = 0.010) were significantly prolonged. The combination therapy also exhibited markedly improved tumor response, achieving superior objective response rates(ORR) for both intrahepatic lesions (61.6% versus 16.4%, P < 0.001) and PVTT (67.1% versus 13.7%, P < 0.001). Conclusion: For HCC with portal vein involvement, the combination of HAIC and SBRT is a more promising and tolerable treatment option compared to HAIC alone.
Keywords: Hepatic arterial infusion chemotherapy, Hepatocellular Carcinoma, Portal vein tumor thrombosis, Propensity score matching, stereotactic body radiation therapy
Received: 16 Dec 2025; Accepted: 09 Feb 2026.
Copyright: © 2026 Zhang, Liu, Zheng, Chen, Wei, Li, Zhong and Zhang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence: Haiming Zhang
Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
