Original Articles
Copyright ©The Author(s) 2001. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Apr 15, 2001; 7(2): 222-227
Published online Apr 15, 2001. doi: 10.3748/wjg.v7.i2.222
Combination of “low-dose” ribavirin and interferon alfa-2a therapy followed by interferon alfa-2a monotherapy in chronic HCV-infected non-responders and relapsers after interferon alfa-2a monotherapy
Perdita Wietzke-Braun, Volker Meier, Felix Braun, Giuliano Ramadori
Perdita Wietzke-Braun, Volker Meier, Felix Braun, Giuliano Ramadori, Abteilung für Gastroenterologie und Endokrinologie, Georg-August-Universität, Göttingen, Germany
Author contributions: All authors contributed equally to the work.
Correspondence to: Professor Dr. Dr. G. Ramadori, Abteilung für Gastroenterologie und Endokrinologie, Georg-August-Universität, Robert-Koch-Strasse 40, 37075 Göttingen, Germany
Telephone: +49-551-39-6301 Fax: +49-551-39-8596
Received: February 6, 2001
Revised: February 26, 2001
Accepted: March 1, 2001
Published online: April 15, 2001
Abstract

AIM: To report on the efficacy, safety and tolerability of interferon alfa-2a combined with a “low dose” of ribavirin for relapsers and non-responders to alpha interferon monotherapy.

METHODS: Thirty four chronic hepatitis C virus infected non responders to interferon alfa-2a monotherapy (a course of at least 3 months treatment) and 13 relapsers to interferon alfa-2a monotherapy (a dose of 3 to 6 million units three times per week for at least 20 weeks but not more than 18 months) were treated with the same dose of interferon alfa-2a used before (3 to 6 million units three times per week) and ribavirin (10 mg/kg daily) for 6 months. In complete responders, interferon alfa-2a was administered for further 6 months at the same dose used before as monotherapy.

RESULTS: Seven (20.6%) of 34 non responders stopped the combined therapy due to adverse events, including two patients with histological and clinical Child A cirrhosis. In 17/27 (63%) non responders, the combined therapy was stopped after three months because of non response. Ten of the 27 non responders completed the 12 month treatment course. At a mean follow up of 28 months (16-37 months) after the treatment, 4/10 (15%) previous non responders still remained complete responders. All 13 previous relapsers completed the 12-month treatment course. At a mean follow up of 22 months (9-36 months) after treatment, 6/13 (46%) the previous relapsers were still sustained complete responders.

CONCLUSION: Our treatment schedule of the combined therapy for 6 months of interferon alfa-2a with a low dose of ribavirin (10 mg/kg/day) followed by 6 months of interferon alfa-2a monotherapy is able to induce a sustained complete response rate in 15% of non responders and 46% of relapsers with chronic hepatitis C virus related liver diseases comparable to those obtained with the standard doses of ribavirin 1000-1200 mg/day. Randomized prospective controlled trials using lower total amounts of ribavirin in combination with interferon should be performed.

Keywords: hepatitis C, chronic/drug therapy, interferon alpha-2a/therapeutic use, interferon alpha-2a/ administration & dosage, ribavirin/administration & dosage, ribavirin/therapeutic use