1. Antiviral therapy and fibrosis progression in patients with mild-moderate hepatitis C recurrence after liver transplantation. A randomized controlled study.
- Author
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Belli LS, Volpes R, Graziadei I, Fagiuoli S, Starkel P, Burra P, Alberti AB, Gridelli B, Vogel W, Pasulo L, De Martin E, Guido M, De Carlis L, Lerut J, Cillo U, Burroughs AK, and Pinzello G
- Subjects
- Adult, Aged, Biopsy, Chi-Square Distribution, Disease Progression, Female, Genotype, Hepacivirus genetics, Hepatitis C complications, Humans, Interferon alpha-2, Liver Cirrhosis virology, Liver Transplantation, Logistic Models, Male, Middle Aged, RNA, Viral blood, Recombinant Proteins therapeutic use, Recurrence, Viral Load, Antiviral Agents therapeutic use, Hepatitis C drug therapy, Interferon-alpha therapeutic use, Liver pathology, Liver Cirrhosis pathology, Polyethylene Glycols therapeutic use, Ribavirin therapeutic use
- Abstract
Backgrounds/aims: We evaluated the effect of antiviral therapy on fibrosis progression in patients with histological features of mild/moderate HCV disease recurrence defined by a Grading score≥4 and Staging score up to 3 (Ishak) at 1 year after liver transplantation., Methods: Seventy-three consecutive patients with mild/moderate recurrence were randomized either to no treatment or to receive Pegilated-Interferon-alfa-2b and ribavirin for 52 weeks. Liver biopsies obtained at baseline (1 year after transplantation) and 2 years afterwards were evaluated for assessment of disease progression, defined as worsening of at least 2 staging points or progression to stage 4 or higher., Results: As for these two major histological end points there were no statistically significant differences between the 2 groups (36.1% vs. 50%, p=0.34 and 36.1% vs. 38.9%, p=1). Fifteen treated patients (41%) achieved a sustained virological response which was associated with a reduced risk of fibrosis worsening for both endpoints when compared to viremic patients (p=0.04)., Conclusions: Although antiviral-therapy was beneficial in preventing fibrosis progression in patients achieving a sustained virological response, the majority of the overall population of our patients with mild-moderate disease recurrence could not benefit from antiviral therapy either because they either could not be treated or did not respond to treatment (EudraCT number: 2005-005760)., (Copyright © 2012. Published by Elsevier Ltd.)
- Published
- 2012
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