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.
Abstract

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