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Published on: September 25, 2019
Treatment of chronic hepatitis C in patients with cirrhosis
1Department of Medicine, Division of Gastroenterology and Hepatology, University of California San Francisco, San Francisco, California, USA.
Insights
Direct-acting antiviral therapies offer a well-tolerated and effective cure for hepatitis C virus (HCV) cirrhosis, improving liver health and reducing mortality. Treatment optimization and safety monitoring are crucial for patients with advanced liver disease.
Area of Science:
- Hepatology
- Virology
- Pharmacology
Background:
- Hepatitis C virus (HCV) infection in cirrhotic patients presents significant management challenges.
- Direct-acting antivirals (DAAs) represent a paradigm shift in HCV treatment.
Purpose of the Study:
- To review treatment options for HCV cirrhosis using approved and emerging DAAs.
- To assess the efficacy and safety of DAA-based therapies in this population.
Main Methods:
- Review of current literature on DAA therapies for HCV cirrhosis.
- Analysis of treatment outcomes, including viral cure, fibrosis progression, and long-term benefits.
- Evaluation of safety concerns and treatment decision factors.
Main Results:
- DAA therapies are well-tolerated and highly effective for achieving viral cure in compensated and decompensated cirrhosis.
- Viral eradication may arrest or reverse fibrosis, reduce liver decompensation, hepatocellular carcinoma, and mortality.
- Optimizing treatment may require longer durations or complex drug combinations; treatment decisions depend on genotype, renal function, drug interactions, and cirrhosis severity.
Conclusions:
- High-potency DAAs have transformed HCV-infected cirrhotic patients from 'difficult-to-treat' to a manageable group.
- Understanding pretreatment factors predicting clinical outcomes is essential for personalized treatment strategies.
Purpose Of Review:
This article reviews treatment options of the approved and soon-to-be approved direct-acting antivirals (DAA)-based therapies in individuals with hepatitis C virus (HCV) cirrhosis.
Recent Findings:
DAA-based therapies have been shown to be well tolerated and effective in achieving viral cure in individuals with compensated and decompensated cirrhosis. Preliminary studies suggest that viral eradication arrests fibrosis progression and could lead to fibrosis regression. Long-term benefits of successful HCV treatment in this population translate into less frequent hepatic decompensation and hepatocellular carcinoma development, improvements in liver disease severity, reduction of liver-related mortality, and potential obviation of the need for transplantation. The optimization of viral eradication rates requires longer duration therapy and/or more complex combinations of drugs, including ribavirin. Treatment decisions are guided by HCV genotype, renal function, drug-drug interactions, and the severity of cirrhosis. Safety concerns are paramount in individuals with advanced liver disease and continued vigilance for hepatotoxicity and other complications is warranted, especially in those with decompensated cirrhosis.
Summary:
The availability of high potency DAA-based therapies with excellent safety profiles has transformed the HCV-infected cirrhotic population into a group that is no longer 'difficult-to-treat'. Understanding the pretreatment factors that predict clinical benefits vs. harm remains key in treating this population.
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