Results of a two-center study comparing hepatic fibrosis progression in HCV-positive liver transplant patients receiving cyclosporine or tacrolimus

Transplant Proc. 2010 Dec;42(10):4573-7. doi: 10.1016/j.transproceed.2010.10.013.

Abstract

A 2-center retrospective analysis was performed in 60 patients undergoing liver transplantation for hepatitis C virus (HCV)-related disease (cyclosporine in 20, tacrolimus in 40). Mean (±SEM) follow-up was 23.6 ± 22.5 and 22.3 ± 13.7 months in patients receiving cyclosporine or tacrolimus, respectively. Clinically indicated biopsies were performed in 15/20 cyclosporine patients (75%) and 22/40 tacrolimus patients (55%; P = .17). The Ishak fibrosis score was significantly lower in cyclosporine-treated patients versus tacrolimus-treated patients (mean 1.7 ± 0.4 vs 3.1 ± 0.4; P = .023), as was percentage of fibrosis grade Ishak ≥4 (7% vs 41%; P = .028). The mean time to moderate fibrosis (Ishak score ≥3) was 38.2 ± 15.1 months in cyclosporine patients (4/15) and 23.5 ± 12.6 months in tacrolimus patients (14/22); the difference was not statistically significant (P = .09). This retrospective study suggests that cyclosporine-based immunosuppression is associated with less severe hepatic fibrosis in HCV-positive liver transplant recipients compared with tacrolimus-based regimens, but a larger prospective comparative trial is necessary to confirm these findings.

Publication types

  • Comparative Study
  • Multicenter Study

MeSH terms

  • Cyclosporine / administration & dosage*
  • Disease Progression
  • Female
  • Hepatitis C / surgery*
  • Humans
  • Immunosuppressive Agents / administration & dosage*
  • Liver Cirrhosis / physiopathology*
  • Liver Transplantation*
  • Male
  • Middle Aged
  • Retrospective Studies
  • Tacrolimus / administration & dosage*

Substances

  • Immunosuppressive Agents
  • Cyclosporine
  • Tacrolimus