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PMID: 15282351 Published · ppublish English Clinical Trial Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Peginterferon Alfa-2a plus ribavirin for chronic hepatitis C virus infection in HIV-infected patients.

The New England journal of medicine ·Vol. 351 ·No. 5 ·2004-07-29 ·Pages 438-50

Torriani FJ, Rodriguez-Torres M, Rockstroh JK, Lissen E, Gonzalez-García J, Lazzarin A, Carosi G, Sasadeusz J, Katlama C, Montaner J, Sette H, Passe S, De Pamphilis J, Duff F, Schrenk UM, Dieterich DT, APRICOT Study Group

Abstract

Hepatitis C virus (HCV) infection is highly prevalent and is associated with substantial morbidity and mortality among persons infected with the human immunodeficiency virus (HIV). We compared the efficacy and safety of pegylated interferon alfa-2a (peginterferon alfa-2a) plus either ribavirin or placebo with those of interferon alfa-2a plus ribavirin for the treatment of chronic HCV infection in patients who were also infected with HIV. A total of 868 persons who were infected with both HIV and HCV and who had not previously been treated with interferon or ribavirin were randomly assigned to receive one of three regimens: peginterferon alfa-2a (180 microg per week) plus ribavirin (800 mg per day), peginterferon alfa-2a plus placebo, or interferon alfa-2a (3 million IU three times a week) plus ribavirin. Patients were treated for 48 weeks and followed for an additional 24 weeks. The primary end point was a sustained virologic response (defined as a serum HCV RNA level below 50 IU per milliliter at the end of follow-up, at week 72). The overall rate of sustained virologic response was significantly higher among the recipients of peginterferon alfa-2a plus ribavirin than among those assigned to interferon alfa-2a plus ribavirin (40 percent vs. 12 percent, P<0.001), or peginterferon alfa-2a plus placebo (40 percent vs. 20 percent, P<0.001). Among patients infected with HCV genotype 1, the rates of sustained virologic response were 29 percent with peginterferon alfa-2a plus ribavirin, 14 percent with peginterferon alfa-2a plus placebo, and 7 percent with interferon alfa-2a plus ribavirin. The corresponding rates among patients infected with HCV genotype 2 or 3 were 62 percent, 36 percent, and 20 percent. Neutropenia and thrombocytopenia were more common among patients treated with regimens that contained peginterferon alfa-2a, and anemia was more common among patients treated with regimens containing ribavirin. Among patients infected with both HIV and HCV, the combination of peginterferon alfa-2a plus ribavirin was significantly more effective than either interferon alfa-2a plus ribavirin or peginterferon alfa-2a monotherapy.

MeSH Terms
Adult Antiviral Agents/adverse effects,therapeutic use Drug Therapy, Combination Female Genotype HIV Infections/complications Hepacivirus/drug effects,genetics Hepatitis C Antibodies/blood Hepatitis C, Chronic/complications,drug therapy Humans Interferon alpha-2 Interferon-alpha/adverse effects,therapeutic use Male Polyethylene Glycols RNA, Viral/blood Recombinant Proteins Ribavirin/adverse effects,therapeutic use
Chemicals
Antiviral Agents Hepatitis C Antibodies Interferon alpha-2 Interferon-alpha RNA, Viral Recombinant Proteins Polyethylene Glycols Ribavirin peginterferon alfa-2b peginterferon alfa-2a
Authors & Affiliations
17 authors, click to expand affiliations / ORCID
Torriani Francesca J
Department of Medicine, Division of Infectious Diseases, University of California, San Diego, AntiViral Research Center, CA 92103, USA. ftorriani@ucsd.edu
Rodriguez-Torres Maribel
Rockstroh Jürgen K
Lissen Eduardo
Gonzalez-García Juan
Lazzarin Adriano
Carosi Giampiero
Sasadeusz Joseph
Katlama Christine
Montaner Julio
Sette Hoel
Passe Sharon
De Pamphilis Jean
Duff Frank
Schrenk Uschi Marion
Dieterich Douglas T
APRICOT Study Group
Article Info
Journal
The New England journal of medicine
Abbr.
N Engl J Med
ISSN
1533-4406
Published
2004-07-29
Pages
438-50
Language
English
Region
United States
NLM ID
0255562
Subset
IM
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