High-dose prolonged combination therapy in non-responders to interferon monotherapy for chronic hepatitis C

Abstract

Background: Therapy of chronic hepatitis C non-responders to interferon monotherapy with standard doses of interferon plus ribavirin is usually ineffective. Aim: To evaluate the efficacy and tolerability of highdose prolonged combination retreatment in non-responder patients. Methods: Patients were retreated for 6 months with 6 Mu αifn on alternate days and 1000 or 1200 mg/ day ribavirin. HCV-RNA negative patients continued therapy for an additional 6 months. Results: Forty patients (29 males, mean age 49,7 years, 34 genotype 1b, 11 with F3 fibrosis) were treated. At 6 months, 20 (50%) patients were HCV-RNA negative but six of them discontinued therapy because of adverse events. A sustained response was achieved in 28% of patients (11/40). A sustained response was more frequent among patients with genotype non-lb than in those with genotype 1b (67 vs. 21%, P = 0.005) and clearance of HCV-RNA in the first 3 months had a high predictive value for sustained response (100% of sustained responders vs. 24% of non-responders, e = 0.0001). Conclusions: High-dose prolonged combination therapy in non-responders to IFN monotherapy leads to a higher rate of sustained response than the standard combination regimen. Tolerabiliity may be a rate-limiting factor. Maximal effectiveness can be predicted in patients with non-lb genotype and in those who clear HCV-RNA soon after starting retreatment.