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Published on: September 30, 2021
Stratification of Hepatocellular Carcinoma Risk Following HCV Eradication or HBV Control
Pierre Nahon1,2,3, Erwan Vo Quang1, Nathalie Ganne-Carrié1,2,3
1AP-HP, Hôpital Avicenne, Liver Unit, 93000 Bobigny, France.
Insights
Hepatocellular carcinoma (HCC) risk persists after viral clearance. New predictors and risk scores can personalize surveillance for patients with advanced liver disease, improving cancer detection.
Area of Science:
- Hepatology
- Oncology
- Virology
Background:
- Effective antiviral therapies for Hepatitis C Virus (HCV) and Hepatitis B Virus (HBV) have reduced hepatocellular carcinoma (HCC) incidence.
- A significant number of patients remain at risk for liver cancer after viral clearance or control, particularly those with advanced fibrosis or cirrhosis.
Purpose of the Study:
- To identify predictors of HCC development in virus-free patients with chronic liver disease.
- To explore the utility of risk scoring systems for stratifying patients based on HCC risk.
- To highlight the need for improved surveillance strategies beyond current guidelines.
Main Methods:
- Review of routine clinical parameters, comorbidities, liver inflammation, and function tests.
- Integration of non-invasive test results into HCC risk scoring systems.
- Analysis of current international guidelines for HCC surveillance in this population.
Main Results:
- Predictors of HCC include comorbidities, persistent liver inflammation, impaired liver function, and non-invasive test results.
- Risk scoring systems can stratify patients into low, intermediate, and high HCC risk groups.
- Current semi-annual ultrasound surveillance has known sensitivity limitations.
Conclusions:
- Personalized HCC management is needed for virus-free patients with chronic liver disease.
- Enhanced surveillance using contrast-enhanced imaging or biomarkers, considering cost-effectiveness, is recommended.
- Refining HCC prediction is crucial for this growing patient population.
Abstract:
Hepatocellular carcinoma (HCC) incidence has dramatically decreased in patients infected with HCV and HBV due to the widespread use of highly effective antiviral agents. Nevertheless, a substantial proportion of patients with advanced fibrosis or cirrhosis following HCV clearance of in case of HBV control whatever the stage of fibrosis remains at risk of liver cancer development. Cancer predictors in these virus-free patients include routine parameters estimating coexisting comorbidities, persisting liver inflammation or function impairment, and results of non-invasive tests which can be easily combined into HCC risk scoring systems. The latter enables stratification according to various liver cancer incidences and allocation of patients into low, intermediate or high HCC risk probability groups. All international guidelines endorse lifelong surveillance of these patients using semi-annual ultrasound, with known sensibility issues. Refining HCC prediction in this growing population ultimately will trigger personalized management using more effective surveillance tools such as contrast-enhanced imaging techniques or circulating biomarkers while taking into account cost-effectiveness parameters.
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