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Published on: September 30, 2021
Future treatment of patients with HCV cirrhosis
Marc Bourlière1, Asma Khaloun, Claire Wartelle-Bladou
1Department of Hepato-Gastroenterology, Hospital Saint Joseph, Marseille, France. mbourliere@hopital-saint-joseph.fr
Insights
Hepatitis C virus (HCV) patients with cirrhosis benefit from new protease inhibitor treatments, though sustained virological response (SVR) rates are lower and side effects higher compared to non-cirrhotic patients.
Area of Science:
- Hepatology
- Virology
- Pharmacology
Background:
- Hepatitis C virus (HCV) infection poses significant risks, particularly for patients with cirrhosis, who experience higher morbidity and mortality.
- Standard treatment with pegylated-interferon (PEG-IFN) and ribavirin (RBV) shows benefits in fibrosis regression but yields lower sustained virological response (SVR) rates in cirrhotic patients.
Purpose of the Study:
- To evaluate the efficacy and outcomes of first-generation protease inhibitors (boceprevir and telaprevir) combined with PR in HCV genotype 1 patients, with a focus on those who have cirrhosis.
Main Methods:
- Comparative analysis of SVR rates in treatment-naïve and treatment-experienced HCV genotype 1 patients with varying fibrosis stages (including cirrhosis).
- Assessment of treatment outcomes with triple regimens (protease inhibitor + PR) versus dual therapy (PR) alone.
Main Results:
- Triple regimens increased SVR by 10-30% in cirrhotic patients compared to PR alone, though this benefit was less pronounced than in non-cirrhotic patients.
- Treatment-experienced patients who previously relapsed showed the greatest SVR improvement with triple therapy, irrespective of fibrosis status.
- Cirrhotic patients, especially prior non-responders, had lower SVR rates, higher relapse rates, and more frequent side effects compared to non-cirrhotic individuals.
Conclusions:
- First-generation protease inhibitors represent an advancement in managing HCV genotype 1 patients with cirrhosis, offering improved SVR rates.
- Despite benefits, careful consideration of lower efficacy and increased adverse events is necessary for cirrhotic patients undergoing these treatments.
Abstract:
Of all hepatitis C virus (HCV) patients, those with cirrhosis are most in need of treatment because of increased morbidity and mortality. Treatment with pegylated-interferon (PEG-IFN) and ribavirin (RBV) (PR) has definitely shown the benefits of successful treatment by improving fibrosis, causing the regression of cirrhosis and reducing and preventing cirrhosis-related complications. However, the sustained virological response (SVR) is lower in patients with cirrhosis. First generation protease inhibitors (boceprevir and telaprevir) in combination with PR are a major advancement in the treatment of both naïve and treatment-experienced genotype 1 patients. In naïve patients, the SVR rate with the triple regimen with boceprevir was increased by 14% in patients with severe fibrosis or cirrhosis compared with PR. This benefit was lower than that observed in patients with mild or moderate fibrosis (30%). The SVR rate of the triple regimen with telaprevir was increased by 10-30% compared with PR in patients with severe fibrosis or cirrhosis compared with nearly 30% in patients with mild or moderate fibrosis. In treatment-experienced patients, previous relapsers have the highest increase in SVR with the triple regimen compared with PR, whatever the status of fibrosis. Previous partial or non-responder patients with cirrhosis had lower SVR rates than those without cirrhosis. However, the benefits of telaprevir and boceprevir vs PR was maintained. Previous non-responder patients with cirrhosis benefited the least from treatment. The relapse rate was always higher and side effects were more frequent in patients with cirrhosis compared with those without. First generation protease inhibitors plus PR appear to be a new step forward in the management of HCV genotype 1 patients with cirrhosis.
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