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World J Gastroenterol. Nov 14, 2006; 12(42): 6861-6864
Published online Nov 14, 2006. doi: 10.3748/wjg.v12.i42.6861
Different doses of consensus interferon plus ribavirin in patients with hepatitis C virus genotype 1 relapsed after interferon monotherapy: A randomized controlled trial
Giuseppe Alaimo, Vito Di Marco, Donatella Ferraro, Rosa Di Stefano, Salvatore Porrovecchio, Francesca D’Angelo, Vincenza Calvaruso, Antonio Craxì, Piero Luigi Almasio
Giuseppe Alaimo, Vito Di Marco, Salvatore Porrovecchio, Francesca D’Angelo, Vincenza Calvaruso, Antonio Craxì, Piero Luigi Almasio, Cattedra di Gastroenterologia, Dipartimento Biomedico di Medicina Interna e Specialistica, University of Palermo, Italy
Donatella Ferraro, Rosa Di Stefano, Cattedra di Virologia, Dipartimento di Igiene e Microbiologia, University of Palermo, Italy
Author contributions: All authors contributed equally to the work.
Correspondence to: Professor Antonio Craxì, Cattedra di Gastroenterologia, Piazza delle Cliniche 2, Palermo 90127, Italy. craxanto@unipa.it
Telephone: +39-91-6552280 Fax: +39-91-6552156
Received: December 28, 2005
Revised: May 19, 2006
Accepted: May 24, 2006
Published online: November 14, 2006
Abstract

AIM: To assess the efficacy of different schedules of consensus interferon (CIFN) plus ribavirin in retreating chronic hepatitis C patients who relapsed after recombinant interferon (rIFN) monotherapy.

METHODS: Forty-five patients (34 males and 11 females) with chronic hepatitis due to hepatitis C virus (HCV) genotype 1 who relapsed after a previous course of rIFN monotherapy were randomized to receive 9 μg CIFN three times per week for 52 wk (group A, n = 22) or 18 μg CIFN three times per week for 52 wk (group B, n = 23) in combination with ribavirin 800 to 1200 mg daily for 52 wk (according to body weight). Virological response was evaluated at week 24 (EVR), at the end of treatment (ETR) and at 76 wk (SVR).

RESULTS: By intention-to-treat analysis, subjects in group A had an EVR in 35% of cases, an ETR in 35% and a SVR in 27.3% of cases. Subjects in group B had an EVR in 32% of cases, an ETR in 35% and a SVR in 26.1% of cases. Treatment was stopped because of adverse effects (mostly intolerance) in 15 patients (6 in group A and 9 in group B). IFN dose reduction was needed in 2 patients (1 in group A and 1 in group B). Ribavirin dose was reduced in 2 patients in group A and 1 in group B respectively. Among the 15 subjects who received at least 80% of the intended schedule, the rate of SVR was 80% (6 in group A and 6 in group B).

CONCLUSION: CIFN in combination with ribavirin when given to HCV genotype 1 relapsers after rIFN monotherapy obtains an unsatisfactory rate of sustained viral clearance independently of dosage of the drug. This may be due to its scarce tolerability.

Keywords: Interferon; Ribavirin; Hepatitis C virus; Hepatitis C; Relapser