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Updated: Feb 18, 2026

An Oncogenic Hepatocyte-Induced Orthotopic Mouse Model of Hepatocellular Cancer Arising in the Setting of Hepatic Inflammation and Fibrosis
Published on: September 12, 2019
Immunotherapy of Hepatocellular Carcinoma: Facts and Hopes
Mercedes Iñarrairaegui1, Ignacio Melero2, Bruno Sangro3
1Liver Unit, Clínica Universidad de Navarra-IDISNA and CIBEREHD, Pamplona, Spain.
Abstract:
Treatment of patients with hepatocellular carcinoma (HCC) in the advanced stage remains a great challenge, with very few drugs approved. After decades of failure of immune therapies, immune checkpoint inhibitors have emerged as potentially effective treatments for patients with HCC in the advanced stage. Immune checkpoints, including human cancer, cytotoxic T-lymphocyte protein 4 (CTLA-4), and programmed cell death protein 1 (PD-1), are surface proteins expressed in a variety of immune cells and mostly provide immunosuppressive signals. Monoclonal antibodies able to block these molecules have shown antitumor activity against a wide spectrum of human cancers. Clinical experience with checkpoint inhibitors in HCC includes early trials with the anti-CTLA-4 agent tremelimumab and a large phase II trial with the anti-PD-1 agent nivolumab. The latter has shown strong activity particularly as second-line therapy, both in terms of tumor response and patient survival. At least three topics should be the focus of future research: (i) the search for activity in patients at less-advanced stages, including the adjuvant treatment of patients with resectable or ablatable tumors; (ii) the enhanced efficacy of combination therapies, including particularly the combination with those targeted and locoregional therapies that may have a synergistic effect or act upon mechanisms of primary or acquired resistance to checkpoint inhibitors; and (iii) the identification of clinical features and serum or tissue biomarkers that would allow a better patient selection for individual treatments. Hopefully, ongoing trials will help to design better treatments in the future. Clin Cancer Res; 24(7); 1518-24. ©2017 AACR.
Insights
Immune checkpoint inhibitors show promise for advanced hepatocellular carcinoma (HCC). Nivolumab, an anti-PD-1 therapy, demonstrates significant efficacy as a second-line treatment, improving patient survival and tumor response.
Area of Science:
- Oncology
- Immunotherapy
Background:
- Advanced hepatocellular carcinoma (HCC) presents significant treatment challenges with limited drug approvals.
- Immune checkpoint inhibitors represent a promising therapeutic avenue after decades of immune therapy failures in HCC.
Purpose of the Study:
- To review the emergence and efficacy of immune checkpoint inhibitors in advanced HCC.
- To highlight key areas for future research in HCC immunotherapy.
Main Methods:
- Review of clinical trials involving immune checkpoint inhibitors, specifically anti-CTLA-4 (tremelimumab) and anti-PD-1 (nivolumab) agents.
- Analysis of nivolumab's activity in a phase II trial for advanced HCC, focusing on second-line therapy outcomes.
Main Results:
- Anti-PD-1 agent nivolumab demonstrated strong activity in second-line treatment for advanced HCC, improving tumor response and patient survival.
- Monoclonal antibodies targeting immune checkpoints like CTLA-4 and PD-1 exhibit antitumor activity across various cancers.
Conclusions:
- Immune checkpoint inhibitors, particularly nivolumab, offer a new treatment strategy for advanced HCC.
- Future research should focus on earlier-stage treatment, combination therapies, and biomarker identification for personalized patient selection.
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