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Updated: Sep 27, 2025

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An Oncogenic Hepatocyte-Induced Orthotopic Mouse Model of Hepatocellular Cancer Arising in the Setting of Hepatic Inflammation and Fibrosis
Published on: September 12, 2019
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Systemic Therapy in Metastatic Hepatocellular Carcinoma
Destry Elms1, Ami Badami1, Asha Dhanarajan2
1Division of Hematology and Oncology, Loyola University Medical Center, Maywood, IL, USA.
Current Gastroenterology Reports
|April 13, 2022
Summary
New systemic therapies, including atezolizumab and bevacizumab, are now standard for advanced hepatocellular carcinoma (HCC). While improving survival, options remain limited for patients with advanced liver disease (Child-Pugh B).
Area of Science:
- Hepatobiliary Oncology
- Medical Oncology
- Pharmacotherapy
Background:
- Advanced hepatocellular carcinoma (HCC) treatment landscape has evolved with novel therapies.
- Tyrosine kinase inhibitors, immunotherapies, and anti-angiogenic agents are now available.
Purpose of the Study:
- To review the evidence supporting new systemic therapies for advanced HCC.
- To evaluate current treatment standards and future directions.
Main Methods:
- Systematic review of clinical trial data and guidelines.
- Analysis of efficacy and safety profiles of novel agents.
Main Results:
- Atezolizumab plus bevacizumab is a new standard of care, replacing sorafenib in first-line therapy for eligible patients.
- Lenvatinib offers an alternative first-line option for patients ineligible for immunotherapy.
- Several second-line treatment options were also detailed, prolonging overall survival.
Conclusions:
- New systemic therapies have significantly improved survival in advanced HCC.
- Current approvals predominantly favor patients with Child-Pugh A classification, highlighting a need for more options in Child-Pugh B disease.
- Further research is required to optimize treatment sequencing and expand therapeutic options for patients with more advanced liver disease.
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