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Published on: February 19, 2019
Determinants of outcome of compensated hepatitis C virus-related cirrhosis
L Serfaty1, H Aumaître, O Chazouillères
1Service d'Hépato-gastroentérologie, Hôpital St-Antoine, Assistance Publique-Hôpitaux de Paris, France.
Insights
Interferon therapy significantly improves survival in patients with compensated hepatitis C virus (HCV)-related cirrhosis. Absence of treatment increases the risk of hepatocellular carcinoma (HCC) and decompensation, highlighting the importance of antiviral therapy.
Area of Science:
- Hepatology and Viral Gastroenterology
- Oncology and Cancer Research
- Clinical Medicine and Therapeutics
Background:
- Hepatitis C virus (HCV)-related cirrhosis, even in compensated stages, carries risks of decompensation, hepatocellular carcinoma (HCC), and mortality.
- Understanding the impact of viral genotype and interferon (IFN) therapy on the prognosis of compensated HCV cirrhosis is crucial for patient management.
Purpose of the Study:
- To evaluate the incidence of decompensation, HCC, and liver transplantation or death in patients with compensated HCV cirrhosis.
- To determine the influence of viral genotype and interferon therapy on the outcomes of these patients.
Main Methods:
- A cohort of 103 patients with compensated HCV-related cirrhosis was followed for a median of 40 months.
- Patients' baseline characteristics, HCV genotypes, and treatment with IFN were recorded.
- Outcomes including cirrhosis complications, HCC development, and survival were assessed using multivariate analysis.
Main Results:
- The 4-year risk of HCC was 11.5%, and the risk of decompensation was 20%.
- Absence of IFN therapy was an independent predictor for both HCC and decompensation.
- IFN-treated patients showed significantly better survival rates (97% at 2 years, 92% at 4 years) compared to untreated patients (95% at 2 years, 63% at 4 years).
Conclusions:
- Complications of cirrhosis are common in compensated HCV cirrhosis, irrespective of viral genotype.
- Absence of interferon therapy is a significant independent predictor of poor outcomes, including HCC, decompensation, and mortality.
- Early antiviral treatment, such as with IFN, is critical for improving survival in patients with compensated HCV cirrhosis.
Abstract:
The aim of this study was to assess the incidence of decompensation (ascites, jaundice, variceal bleeding, and encephalopathy), hepatocellular carcinoma (HCC) and death or liver transplantation in patients with compensated hepatitis C virus (HCV)-related cirrhosis, taking into account the viral genotype and interferon (IFN) therapy. Between 1989 and 1994, 668 patients with no clinical evidence of decompensation were referred to our department for liver biopsy because of positivity for anti-HCV antibodies and elevated aminotransferase activity; 103 of these patients had cirrhosis. The median follow-up was 40 months. Fifty-nine patients were treated with IFN for a mean duration of 11+/-6 months; 3 (5%) had a prolonged biochemical and virological response. Baseline characteristics of IFN-treated and untreated patients were not significantly different. HCV genotypes (InnoLiPa) were predominantly 1b (48%) and 3a (20%). During follow-up, complications of cirrhosis occurred in 26 patients, HCC in 11 patients, and decompensation not related to HCC in 19 patients. Sixteen patients died, 94% of liver disease. Three patients were transplanted for liver failure. The 4-year risk of HCC was 11.5% (annual incidence 3.3%) and that of decompensation was 20%. Survival probability was 96% and 84% at 2 and 4 years, respectively. In multivariate analysis, the absence of IFN therapy was the only independent factor predictive both for HCC and decompensation. A low albumin level at entry and the absence of IFN therapy were the two independent factors predictive of death or liver transplantation. Probability of survival at 2 and 4 years was significantly different between IFN-treated and untreated patients (respectively 97% and 92% vs 95% and 63%, P < .0001). In conclusion, in patients with compensated HCV-related cirrhosis: 1) complications of cirrhosis are frequent, whatever the viral genotype; and 2) the severity of cirrhosis and the absence of IFN therapy are independently predictive of bad outcome.
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