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Predictors of functional benefit of hepatitis C therapy in a 'real-life' cohort
Niels Steinebrunner1, Kerstin Stein2, Catharina Sandig1
1Department of Internal Medicine IV, University Hospital Heidelberg, Heidelberg 69120, Germany.
Insights
Direct-acting antivirals (DAAs) achieve high viral clearance in chronic hepatitis C virus (HCV) patients with cirrhosis. Child-Pugh score, MELD score, platelets, albumin, and bilirubin predict functional benefit beyond viral eradication.
Area of Science:
- Hepatology
- Virology
- Clinical Medicine
Background:
- Chronic hepatitis C virus (HCV) infection with liver cirrhosis poses significant health challenges.
- Direct-acting antivirals (DAAs) offer a promising treatment modality for HCV infection.
Purpose of the Study:
- To identify predictors of functional benefit from DAAs in patients with chronic HCV and liver cirrhosis.
- To assess the impact of antiviral therapy on liver function markers.
Main Methods:
- A cohort of 199 patients with chronic HCV genotypes 1-4 and liver cirrhosis (compensated and decompensated) were analyzed.
- Patients received 12 or 24 weeks of combination DAA therapy.
- Binary logistic regression was used to identify predictors of functional benefit.
Main Results:
- Viral clearance was achieved in 88% of patients, with sustained virological response (SVR12) rates varying by genotype.
- Improvements in MELD scores were observed in 37% of patients.
- Child-Pugh score, MELD score, platelet count, albumin, and bilirubin levels were significant predictors of functional benefit.
Conclusions:
- DAA therapy is effective in achieving viral clearance in HCV patients with advanced liver disease.
- Specific clinical and laboratory parameters predict functional improvement, aiding in personalized treatment decisions.
Aim:
To define predictors of functional benefit of direct-acting antivirals (DAAs) in patients with chronic hepatitis C virus (HCV) infection and liver cirrhosis.
Methods:
We analysed a cohort of 199 patients with chronic HCV genotype 1, 2, 3 and 4 infection involving previously treated and untreated patients with compensated (76%) and decompensated (24%) liver cirrhosis at two tertiary centres in Germany. Patients were included with treatment initiation between February 2014 and August 2016. All patients received a combination regimen of one or more DAAs for either 12 or 24 wk. Predictors of functional benefit were assessed in a univariable as well as multivariable model by binary logistic regression analysis.
Results:
Viral clearance was achieved in 88% (175/199) of patients. Sustained virological response (SVR) 12 rates were as follows: among 156 patients with genotype 1 infection the SVR 12 rate was 90% (n = 141); among 7 patients with genotype 2 infection the SVR 12 rate was 57% (n = 4); among 30 patients with genotype 3 infection the SVR 12 rate was 87% (n = 26); and among 6 patients with genotype 4 infection the SVR 12 rate was 67% (n = 4). Follow-up MELD scores were available for 179 patients. A MELD score improvement was observed in 37% (65/179) of patients, no change of MELD score in 41% (74/179) of patients, and an aggravation was observed in 22% (40/179) of patients. We analysed predictors of functional benefit from antiviral therapy in our patients beyond viral eradication. We identified the Child-Pugh score, the MELD score, the number of platelets and the levels of albumin and bilirubin as significant factors for functional benefit.
Conclusion:
Our data may contribute to the discussion of potential risks and benefits of antiviral therapy with individual patients infected with HCV and with advanced liver disease.
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