Interferon alpha 2b and ribavirin for the treatment of recurrent hepatitis C after liver transplantation: Cohort study of 38 patients

Sandeep Mukherjee, Elizabeth Lyden, Timothy M. McCashland, Daniel F. Schafer

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22 Citations (Scopus)

Abstract

Aim: Recurrent hepatitis C virus (HCV) is universal following liver transplantation. Patients are often treated with interferon and ribavirin in an attempt to eradicate the virus. We describe our experience with 38 patients with recurrent HCV from a single liver transplant program. Methods: Between October 2000 and November 2001, 38 patients with recurrent HCV were treated with interferon alpha 2b 3 million units three times a week and ribavirin 1000-1200 mg per day. HCV RNA and liver biopsies were performed before treatment at the end of treatment (EOT), and 6 months after EOT in patients who were HCV RNA negative at EOT. Results: There were 29 males and nine females. Median age was 49 years. In total, 34 patients were genotype 1 and two each were genotype 3 and 4. Six patients received HCV positive donors and 24 patients (63%) completed treatment. The most common indication for discontinuation of treatment was severe fatigue in 14 patients (37%). On intention to treat analysis, a sustained biochemical and virological response occurred in 10 patients (26%). Unchanged or improved fibrosis scores were present in 37% of patients, of whom 71% were non-responders to therapy. Conclusions: Interferon alpha 2b and ribavirin were poorly tolerated in this series of recurrent HCV patients, with sustained HCV eradication occurring in only 26% of patients. However, the majority of non-responders demonstrated unchanged or improved fibrosis scores, suggesting that a subset of patients may benefit from maintenance antiviral therapy to prevent the development of cirrhosis.

Original languageEnglish
Pages (from-to)198-203
Number of pages6
JournalJournal of Gastroenterology and Hepatology (Australia)
Volume20
Issue number2
DOIs
StatePublished - 2005
Externally publishedYes

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interferon alfa-2b
Ribavirin
Hepatitis C
Liver Transplantation
Cohort Studies
Hepacivirus
Therapeutics
Fibrosis

All Science Journal Classification (ASJC) codes

  • Gastroenterology
  • Hepatology

Cite this

Interferon alpha 2b and ribavirin for the treatment of recurrent hepatitis C after liver transplantation : Cohort study of 38 patients. / Mukherjee, Sandeep; Lyden, Elizabeth; McCashland, Timothy M.; Schafer, Daniel F.

In: Journal of Gastroenterology and Hepatology (Australia), Vol. 20, No. 2, 2005, p. 198-203.

Research output: Contribution to journalArticle

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abstract = "Aim: Recurrent hepatitis C virus (HCV) is universal following liver transplantation. Patients are often treated with interferon and ribavirin in an attempt to eradicate the virus. We describe our experience with 38 patients with recurrent HCV from a single liver transplant program. Methods: Between October 2000 and November 2001, 38 patients with recurrent HCV were treated with interferon alpha 2b 3 million units three times a week and ribavirin 1000-1200 mg per day. HCV RNA and liver biopsies were performed before treatment at the end of treatment (EOT), and 6 months after EOT in patients who were HCV RNA negative at EOT. Results: There were 29 males and nine females. Median age was 49 years. In total, 34 patients were genotype 1 and two each were genotype 3 and 4. Six patients received HCV positive donors and 24 patients (63{\%}) completed treatment. The most common indication for discontinuation of treatment was severe fatigue in 14 patients (37{\%}). On intention to treat analysis, a sustained biochemical and virological response occurred in 10 patients (26{\%}). Unchanged or improved fibrosis scores were present in 37{\%} of patients, of whom 71{\%} were non-responders to therapy. Conclusions: Interferon alpha 2b and ribavirin were poorly tolerated in this series of recurrent HCV patients, with sustained HCV eradication occurring in only 26{\%} of patients. However, the majority of non-responders demonstrated unchanged or improved fibrosis scores, suggesting that a subset of patients may benefit from maintenance antiviral therapy to prevent the development of cirrhosis.",
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