Evidence map›Paper›PMID 42434222›Full record

ArticleJournal of gastrointestinal oncology2026

Sequential surgery following conversion therapy based on combination of immune checkpoint inhibitors and antiangiogenic targeted drugs as a potential approach for advanced hepatocellular carcinoma with portal vein tumor thrombus: a prospective study.

Shang Gao, Yanqin Hu, Yinbiao Cao, Weizheng Liu, Hongxiang Jiang, Tong Jiang, Haowen Tang, Shichun Lu

Abstract read
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Article in Journal of gastrointestinal oncology, 2026. 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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1 · What the graph read from it

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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

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Shang Gao *School of Medicine, Nankai University, Tianjin, China.
Yanqin Hu *School of Medicine, Nankai University, Tianjin, China.
Yinbiao CaoFaculty of Hepato-Pancreato-Biliary Surgery, Chinese People's Liberation Army General Hospital, Beijing, China.
Weizheng LiuSchool of Medicine, Nankai University, Tianjin, China.
Hongxiang JiangFaculty of Hepato-Pancreato-Biliary Surgery, Chinese People's Liberation Army General Hospital, Beijing, China.
Tong JiangDepartment of Medical Psychology, the Eighth Medical Center of Chinese People's Liberation Army General Hospital, Beijing, China.
Haowen TangSchool of Medicine, Nankai University, Tianjin, China.
Shichun LuFaculty of Hepato-Pancreato-Biliary Surgery, Chinese People's Liberation Army General Hospital, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Hepatocellular carcinoma (HCC) patients with portal vein tumor thrombus (PVTT) face a very poor prognosis. And it remains unclear whether sequential surgery following conversion therapy based on immunotherapy combined with targeted therapy can yield long‑term survival benefits. This study aims to evaluate the long-term efficacy and safety of hepatocellular carcinoma patients with portal vein tumor thrombus receiving sequential surgery following conversion therapy with a combination of targeted therapy and immunotherapy, thereby demonstrating the therapeutic potential of this regimen. Methods: Data from 76 HCC patients with PVTT treated with programmed death-1 (PD-1) inhibitors and tyrosine kinase inhibitors (TKIs) followed by surgical treatment at Chinese People's Liberation Army General Hospital (June 2019 to June 2024) were analyzed. Recurrence-free survival (RFS) and overall survival (OS) were primary endpoints. Results: The median RFS was 21 months; the median OS was 62 months. RFS rates at 6 months, 1 year, 2 years, and 3 years were 76.2%, 59.7%, 48.1%, and 42.5%, respectively. OS rates at 6 months, 1 year, 2 years, 3 years, and 5 years were 98.7%, 93.4%, 78.1%, 72.4%, and 45.5%, respectively. Cox regression showed that preoperative alpha-fetoprotein (AFP) ≥20 ng/mL was an independent mortality factor, while non-major-pathological-response (non-mPR) and tumor size >50 mm were independent recurrence factors. Adverse events and surgical complications were evaluated, with no patient deaths resulting from conversion therapy or sequential radical surgery. Conclusions: For HCC patients with PVTT who achieve successful conversion and undergo radical surgery, sequential surgery following conversion therapy based on combination of immune checkpoint inhibitors (ICIs) and anti-angiogenic targeted drugs (AATDs) is associated with favorable RFS and OS, and appears safe and effective. These findings suggest that this regimen may represent a promising option for these patients.

Indexed as

conversion therapyHepatocellular carcinoma (HCC)portal vein tumor thrombus (PVTT)surgical resection

Identifiers

PMID42434222
PMCPMC13350586

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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.