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Updated: Jul 13, 2026

A Protocol for Analyzing Hepatitis C Virus Replication
Published on: June 26, 2014
Antiviral therapy for chronic hepatitis C in patients with inherited bleeding disorders: an international,
D Posthouwer1, T T Yee, M Makris
1Van Creveldkliniek, University Medical Center, Utrecht, The Netherlands.
Insights
Antiviral therapy for hepatitis C in hemophilia patients achieved sustained virological response (SVR) in up to 63% of cases. Successful treatment significantly reduced the risk of end-stage liver disease (ESLD) long-term.
Area of Science:
- Hepatology
- Virology
- Hematology
Background:
- Hepatitis C virus (HCV) infection is a significant comorbidity in individuals with hemophilia.
- Limited data exists regarding the long-term efficacy and outcomes of antiviral treatments for HCV in this population.
Purpose of the Study:
- To evaluate the effectiveness of interferon-based (IFN-based) therapies in achieving HCV eradication.
- To identify factors influencing treatment response.
- To assess the incidence of end-stage liver disease (ESLD) post-treatment.
Main Methods:
- A multicenter cohort study included 295 treatment-naïve hemophilia patients with chronic HCV infection.
- Sustained virological response (SVR) was the primary measure of treatment efficacy.
- Odds ratios (ORs) were used to determine factors associated with treatment response, and Kaplan-Meier survival analysis assessed ESLD cumulative incidence.
Main Results:
- SVR rates varied by treatment regimen and HIV co-infection status, reaching 63% with pegylated IFN (PegIFN) and ribavirin in HIV-negative patients.
- HCV genotypes 2 and 3, and combination therapies (IFN/ribavirin or PegIFN/ribavirin) were associated with higher SVR rates.
- No relapses or ESLD occurred in patients achieving SVR up to 15 years post-treatment, whereas unsuccessfully treated patients had a 13.0% cumulative incidence of ESLD.
Conclusions:
- Effective antiviral therapy provides a lasting benefit for hemophilia patients with HCV.
- Achieving SVR significantly mitigates the long-term risk of developing end-stage liver disease.
Background:
Hepatitis C is a major co-morbidity in patients with hemophilia. However, there is little information on the efficacy of antiviral therapy and long-term follow-up after treatment.
Objectives:
To assess the effect of interferon-based (IFN-based) therapy on hepatitis C virus (HCV) eradication, to identify determinants associated with treatment response, and to assess the occurrence of end-stage liver disease (ESLD) after completing antiviral therapy.
Patients And Methods:
In a multicenter cohort study, 295 treatment-naïve hemophilia patients chronically infected with HCV were included. The effect of therapy was expressed as sustained virological response (SVR). Determinants associated with treatment response were expressed as odds ratios (ORs). Cumulative incidence of ESLD was assessed using a Kaplan-Meier survival table.
Results:
Among human immunodeficiency virus (HIV) negative patients (n = 235), SVR was 29% (29/101) for IFN monotherapy, 44% (32/72) for IFN with ribavirin, and 63% (39/62) for pegylated IFN (PegIFN) with ribavirin. In patients co-infected with HIV (n = 60), IFN monotherapy, IFN with ribavirin, and PegIFN with ribavirin eradicated HCV in 7/35 (20%), 1/2 (50%), and 11/23 (48%), respectively. SVR increased with genotype 2 and 3 [OR 11.0, 95% CI: 5.8-20.5], and combination therapy (IFN and ribavirin OR 3.7, 95% CI: 1.7-8.4), PegIFN and ribavirin (OR 4.2, 95% CI: 1.8-9.5). Up to 15 years after antiviral treatment, none of the patients with a SVR relapsed and none developed ESLD. In contrast, among unsuccessfully treated patients the cumulative incidence of ESLD after 15 years was 13.0%.
Conclusions:
Successful antiviral therapy appears to have a durable effect and reduces the risk of ESLD considerably.
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