Treatment of recurrent HCV infection following liver transplantation: results of a multicenter, randomized, versus placebo, trial of ribavirin alone as maintenance therapy after one year of PegIFNα-2a plus ribavirin

J Hepatol. 2012 Sep;57(3):564-71. doi: 10.1016/j.jhep.2012.04.022. Epub 2012 May 18.

Abstract

Background & aims: We aimed at determining the effect of maintenance therapy with ribavirin alone, after a year of combined peginterferon-alfa 2a (PegIFNα-2a) and ribavirin therapy, on viral response and liver histology after liver transplantation (LT).

Methods: Hundred and one patients with recurrent HCV and a minimum of stage 1 fibrosis (METAVIR scoring), 1-5years after LT, were enrolled. PegIFNα-2a and ribavirin were initiated at 90 μg/wk and 600 mg/d, respectively, then increased or adjusted as a function of tolerance. At 12 months, combination therapy was discontinued and patients were randomized to ribavirin or placebo for a further 12 months. Growth factor use was permitted.

Results: At 18 months, a sustained virological response (SVR) was obtained in 47.9% of patients in Per Protocol (PP) analysis, and was higher in patients with genotype 2 or 3 than in patients with genotype 1 or 4, in patients with genotypes 1+4 receiving ciclosporine than in those receiving tacrolimus, in patients with worse renal function, in those having received EPO, in patients with lower weight, and in those with lower viral load at 3 months. Using logistic regression, only the early viral response, recipient weight and renal function were independently associated with better SVR. SVR, viral load, activity, and fibrosis scores were similar, at M18 and M30, in patients randomized to ribavirin, or to placebo.

Conclusions: A PP SVR was achieved in 47.9% of patients with established recurrent hepatitis C after LT. Maintenance therapy with ribavirin alone does not improve the virological response or the histological parameters.

Publication types

  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antiviral Agents / adverse effects
  • Antiviral Agents / therapeutic use*
  • Cyclosporine / therapeutic use
  • Double-Blind Method
  • Drug Therapy, Combination / adverse effects
  • Female
  • Genotype
  • Hepacivirus / physiology
  • Hepatitis C / complications
  • Hepatitis C / drug therapy*
  • Hepatitis C / pathology
  • Humans
  • Immunosuppressive Agents / therapeutic use
  • Induction Chemotherapy
  • Interferon-alpha / adverse effects
  • Interferon-alpha / therapeutic use*
  • Kidney / physiology
  • Liver Cirrhosis / complications
  • Liver Cirrhosis / pathology
  • Liver Transplantation
  • Logistic Models
  • Maintenance Chemotherapy
  • Male
  • Middle Aged
  • Placebos / therapeutic use
  • Polyethylene Glycols / adverse effects
  • Polyethylene Glycols / therapeutic use*
  • Recombinant Proteins / adverse effects
  • Recombinant Proteins / therapeutic use
  • Recurrence
  • Ribavirin / adverse effects
  • Ribavirin / therapeutic use*
  • Tacrolimus / therapeutic use
  • Treatment Outcome
  • Viral Load

Substances

  • Antiviral Agents
  • Immunosuppressive Agents
  • Interferon-alpha
  • Placebos
  • Recombinant Proteins
  • Polyethylene Glycols
  • Ribavirin
  • Cyclosporine
  • peginterferon alfa-2a
  • Tacrolimus