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Published on: June 26, 2014
Predictors of sustained virological response in patients with hepatitis C virus genotype 3 infection
Dorota Zarębska-Michaluk1, Dariusz Lebensztejn2, Magdalena Chrapek3
1Clinic of Infectious Diseases, Regional Polyclinical Hospital, Kielce, Poland.
Insights
Predictors of sustained virological response (SVR) in chronic hepatitis C virus (HCV) genotype 3 patients treated with standard therapy were identified. Low platelet count and elevated GGT indicate poor response, while rapid and early virological response predicts SVR.
Area of Science:
- Hepatology
- Virology
- Internal Medicine
Background:
- Chronic hepatitis C virus (HCV) genotype 3 infection poses a significant global health challenge.
- Standard therapy with pegylated interferon alpha (PegIFNα) and ribavirin (RBV) has been a cornerstone treatment for HCV.
- Identifying predictors of treatment success is crucial for optimizing patient outcomes.
Purpose of the Study:
- To evaluate factors associated with sustained virological response (SVR) in treatment-naïve patients with HCV genotype 3.
- To determine the predictive value of early virological response markers for SVR.
Main Methods:
- Retrospective analysis of 116 treatment-naïve patients with HCV genotype 3 receiving 24 weeks of PegIFNα and RBV.
- Assessment of pretreatment factors, including liver biopsy, platelet count, and gamma-glutamyl transferase (GGT) levels.
- Measurement of HCV RNA at weeks 4 (rapid virological response - RVR) and week 12 (early virological response - EVR).
Main Results:
- An overall SVR rate of 70.7% was achieved.
- Univariate analysis showed younger age, mild fibrosis, normal GGT, and normal platelet count predicted higher SVR.
- Multivariate analysis identified baseline platelet count > 140,000/µl and normal GGT as significant predictors of SVR.
- RVR was achieved by 34.1% of patients, and EVR by 84.8%.
- Patients achieving RVR had a significantly higher SVR rate (p = 0.002).
Conclusions:
- Low baseline platelet count and elevated GGT activity are associated with poor response to PegIFNα and RBV in HCV genotype 3 infection.
- Achieving rapid and early virological response strongly predicts a higher likelihood of SVR.
- These findings aid in predicting treatment outcomes for HCV genotype 3 patients receiving standard therapy.
Aim Of The Study:
To assess predictors of sustained virological response (SVR) in patients with chronic hepatitis C virus (HCV) genotype 3 treated with standard therapy.
Material And Methods:
We retrospectively investigated data of 116 consecutive treatment-naïve patients chronically infected with HCV genotype 3, treated with pegylated interferon alpha (PegIFNα) and ribavirin (RBV) for 24 weeks. HCV RNA at week 4 (rapid virological response - RVR) and week 12 (early virological response - EVR) were measured in 85 and 105 patients respectively. Liver biopsy data were available for 103 patients. The variables were compared between patients with an SVR and those without.
Results:
Overall 70.7% of patients achieved an SVR. Pretreatment factors including younger age, mild liver fibrosis as well as normal values of gamma-glutamyl transferase (GGT) and platelet count were significantly associated with higher SVR rate in univariate analysis. In the multivariate analysis only baseline platelet count > 140 000/µl and normal GGT activity were correlated with higher SVR rate. At weeks 4 and 12 HCV RNA was undetectable in 34.1% and 84.8% of patients respectively. The SVR rate was significantly higher in patients with an RVR compared to those without (p = 0.002). Only 2 patients with a rapid and early virological response did not achieve an SVR; both had negative pretreatment prognostic factors.
Conclusions:
In treatment-naïve patients with genotype 3 HCV infection, low baseline platelet count and elevated GGT activity were significantly associated with poor response to PegIFNα and RBV. Achieving a rapid and early virological response was associated with higher likelihood of an SVR.
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