Abstract

Sustained response to interferon treatment for chronic hepatitis C is unsatisfactory. This study examined whether combining interferon alfa with ribavirin induces a better sustained efficacy than interferon alone in the treatment of chronic hepatitis C. Sixty noncirrhotic patients with chronic hepatitis C were randomly assigned to three groups. Group 1 received 1200 mg oral ribavirin daily plus 3 million units of recombinant interferon alfa 2a thrice weekly for 24 weeks, group 2 received the same dose of interferon alfa 2a alone for 24 weeks, and group 3 received no treatment. The patients were then followed up for an additional 96 weeks. At the end of treatment, a complete response (normal serum alanine aminotransferase level and undetectable serum hepatitis C virus RNA) was achieved in 16 of the 21 patients in group 1 (76%), as compared with 6 of 19 in group 2 (32%) and none in group 3. At 96 weeks after the end of treatment, patients in group 1 sustained a higher complete response rate than patients in group 2 (43% vs. 6%). Combined treatment with ribavirin and interferon alfa 2a for 24 weeks is more effective than interferon alfa 2a alone for the treatment of chronic hepatitis C. The biochemical and virological responses were sustained in about one half of the treated patients for at least 2 years after cessation of the therapy.

Keywords

RibavirinMedicineInterferon alfaGastroenterologyInternal medicineInterferonChronic hepatitisAlpha interferonHepatitis CPeginterferon alfa-2aHepatitis C virusImmunologyVirus

MeSH Terms

AdultAgedAlanine TransaminaseChronic DiseaseDrug TherapyCombinationFemaleHepatitis CHumansInterferon alpha-2Interferon-alphaLiverMaleMiddle AgedRNAViralRecombinant ProteinsRibavirin

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Publication Info

Year
1996
Type
article
Volume
111
Issue
5
Pages
1307-1312
Citations
247
Access
Closed

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247
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2
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Cite This

Lai My, Jia‐Horng Kao, Pei‐Ming Yang et al. (1996). Long-term efficacy of ribavirin plus interferon alfa in the treatment of chronic hepatitis C. Gastroenterology , 111 (5) , 1307-1312. https://doi.org/10.1053/gast.1996.v111.pm8898645

Identifiers

DOI
10.1053/gast.1996.v111.pm8898645
PMID
8898645

Data Quality

Data completeness: 81%