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A Competent Hepatocyte Model Examining Hepatitis B Virus Entry through Sodium Taurocholate Cotransporting Polypeptide as a Therapeutic Target
Published on: May 10, 2022
[Progress of antiviral therapy for hepatitis C virus-related decompensated cirrhosis]
1Department of Traditional and Western Medical Hepatology, Third Hospital of Hebei Medical University, Shijiazhuang 050051, China.
Insights
Direct-acting antiviral agents (DAAs) offer a safe treatment for hepatitis C virus-related decompensated cirrhosis. Sofosbuvir-based regimens achieve high sustained virological response rates and improve liver function, reducing transplant needs.
Area of Science:
- Hepatology
- Virology
- Pharmacology
Background:
- Direct-acting antiviral agents (DAAs) are primary treatments for hepatitis C virus (HCV)-related decompensated cirrhosis.
- NS3/4A protease inhibitors are not recommended due to liver metabolism.
- Recent guidelines favor sofosbuvir (SOF)-based regimens.
Purpose of the Study:
- To evaluate the efficacy and safety of SOF-based DAAs in patients with HCV-related decompensated cirrhosis.
- To assess the impact of DAAs on liver function and the need for liver transplantation.
Main Methods:
- Review of SOF-based regimens including SOF/velpatasvir, SOF/daclatasvir, and SOF/ledipasvir.
- Analysis of sustained virological response (SVR) rates at 12/24 weeks.
- Evaluation of liver reserve function improvement and reduction in liver transplantation requirements.
Main Results:
- SOF-based regimens achieve high SVR rates (88%–100%).
- Significant improvement in liver reserve function observed in 42%–53% of patients.
- Reduced need for liver transplantation, with 15.5%–49% avoiding it short-term and 10.3%–19.2% specifically with SOF/LDV or SOF/DCV.
Conclusions:
- SOF-based DAAs represent a safe and effective antiviral strategy for HCV-related decompensated cirrhosis.
- These treatments improve patient outcomes and decrease the burden on liver transplantation waiting lists.
Abstract:
Direct-acting antiviral agents (DAAs) are the main antiviral therapeutics for hepatitis C virus-related decompensated stage cirrhosis. DAAs of NS3/4A protease inhibitors use is not recommended for patients with decompensated cirrhosis due to characteristics of DAAs metabolism in liver. The recent guidelines have recommended sofosbuvir (SOF)-based plan including pan-genotype plan of sofosbuvir(SOF)/velpatasvir (VEL), sofosbuvir combined with daclatasvir (DCV), genotype 1,4,5,6 specific plan of sofosbuvir (SOF) / ledipasvir (LDV) for 24 weeks or above in combination with ribavirin for 12 weeks because NS5B and NS5A inhibitors has no obvious effect on CYP450 enzyme system and achievement of sustained virological response (SVR) rates at 12/24 weeks is achievable in 88% ~ 100%, and liver reserve function improves in 42% ~ 53% of patients. Furthermore, approximately 15.5% ~ 49% of patients waiting for liver transplantation after treatment with DAAs do not require liver transplantation for short-term and 10.3% ~19.2% of patients receiving SOF/LDV, and SOF combined with DCV not needed liver transplantation. Thus, the clinical application of DAAs provides a safe and reliable antiviral treatment plan for hepatitis C virus-related decompensated stage cirrhosis.
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