Evidence map›Paper›PMID 41357237›Full record

ArticleFrontiers in immunology2025

Complete response and HBsAg clearance of advanced hepatocellular carcinoma associated with hepatitis B by DEB-TACE combined systematic therapy: a case report.

Baiguo Xu, Yufeng Cui, Hao Cui, Ning Wang, Zhongsong Gao, Qing Ye

Abstract readCase Reports
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. Not yet cited in PubMed.

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1 · What the graph read from it

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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

6 authors.

Baiguo XuDepartment of Gastroenterology and Hepatology, Tianjin Third Central Hospital, Tianjin, China.
Yufeng CuiDepartment of Gastroenterology and Hepatology, Tianjin Third Central Hospital, Tianjin, China.
Hao CuiDepartment of Gastroenterology and Hepatology, Tianjin Third Central Hospital, Tianjin, China.
Ning WangDepartment of Gastroenterology and Hepatology, Tianjin Third Central Hospital, Tianjin, China.
Zhongsong GaoDepartment of Gastroenterology and Hepatology, Tianjin Third Central Hospital, Tianjin, China.
Qing YeDepartment of Gastroenterology and Hepatology, Tianjin Third Central Hospital, Tianjin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Systemic therapy is the standard treatment for patients with hepatitis B-related hepatocellular carcinoma (HCC) and portal vein invasion. Emerging evidence suggests that the combination of localized regional therapy, multikinase inhibitors (MKIs), and immune checkpoint inhibitors (ICIs) yields promising outcomes for advanced HCC. ICIs not only effectively control HCC progression but may also facilitate a HBsAg clearance for hepatitis B-associated HCC patients, characterized by sustained HBV DNA (Hepatitis B Virus Deoxyribonucleic Acid)and HBsAg clearance. This report details a case of hepatitis B cirrhosis with multifocal intrahepatic HCC and portal vein involvement, where the patient achieved complete response (CR) and HBsAg clearance following treatment with lenvatinib (an MKI), tislelizumab (a PD-1 inhibitor), and localized regional therapy. Case summary: A 61-year-old male with hepatitis B-related cirrhosis and advanced HCC with portal vein involvement underwent drug-loaded microsphere hepatic arterial chemoembolization (DEB-TACE) treatment. Additionally, the patient received a combination therapy of lenvatinib and tislelizumab. Following three DEB-TACE sessions, six months of lenvatinib, and seven cycles of tislelizumab, the patient attained CR and achieved HBsAg clearance of hepatitis B, as evidenced by the sustained absence of HBV DNA and HBsAg. Conclusion: The concurrent administration of DEB-TACE, lenvatinib, and tislelizumab demonstrated efficacy in achieving a HBsAg clearance for hepatitis B in a patient presenting with advanced HCC and portal vein tumor thrombosis. These findings suggest that a localized regimen incorporating MKIs and ICIs holds promise as a therapeutic approach for select cases of HBV-HCC, potentially leading to a HBsAg clearance of hepatitis B. Large-scale studies are warranted to validate these findings.

Indexed as

Carcinoma, HepatocellularChemoembolization, TherapeuticHepatitis BHepatitis B Surface AntigensLiver NeoplasmsAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsCombined Modality TherapyHepatitis B virusHumansImmune Checkpoint InhibitorsMaleMiddle AgedPhenylurea CompoundsQuinolinesTreatment OutcomeAntibodies, Monoclonal, HumanizedHepatitis B Surface AntigensImmune Checkpoint InhibitorslenvatinibPhenylurea CompoundsQuinolinestislelizumabDEB-TACEHBsAg clearancehepatocellular carcinomaimmunotherapylenvatiniblocal-regional therapytislelizumab

Identifiers

PMID41357237
PMCPMC12675470

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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.