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PMID: 15598915 Published · ppublish English Clinical Trial Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Pegylated interferon alfa-2b vs standard interferon alfa-2b, plus ribavirin, for chronic hepatitis C in HIV-infected patients: a randomized controlled trial.

JAMA ·Vol. 292 ·No. 23 ·2004-12-15 ·Pages 2839-48

Carrat F, Bani-Sadr F, Pol S, Rosenthal E, Lunel-Fabiani F, Benzekri A, Morand P, Goujard C, Pialoux G, Piroth L, Salmon-Céron D, Degott C, Cacoub P, Perronne C, ANRS HCO2 RIBAVIC Study Team

Abstract

Treatment of chronic hepatitis C virus (HCV) infection in human immunodeficiency virus (HIV)-infected patients is a growing concern. Most data on the virologic efficacy and safety of the combination of peginterferon alfa-2b and ribavirin in coinfected patients come from uncontrolled studies. To study the safety and efficacy of peginterferon alfa-2b plus ribavirin vs standard interferon alfa-2b plus ribavirin in HIV-HCV coinfected patients. A multicenter, randomized, parallel-group, open-label trial. Patients were enrolled from February 2000 to February 2002 and followed up for 72 weeks. Four hundred twelve HIV-HCV coinfected patients with detectable serum HCV-RNA, abnormal liver histology, a CD4 cell count of at least 200 x 10(6)/L, and stable plasma HIV-RNA. Treatment with ribavirin 400 mg twice a day, orally, plus either peginterferon alfa-2b (1.5 microg/kg subcutaneous injection once a week) or standard interferon alfa-2b (3 million units of subcutaneous injection 3 times a week) for 48 weeks. Sustained virologic response, defined by undetectable serum HCV-RNA at week 72. More patients had sustained virologic responses in the peginterferon group than in the standard interferon group (27% vs 20%, P = .047). This difference between the treatments was found in patients with HCV genotype 1 or 4 infection (17% for peginterferon vs 6% for standard interferon, P = .006) but was not found in patients with HCV genotype 2, 3, or 5 (44% for peginterferon vs 43% for standard interferon, P = .88). Together, a decline in HCV-RNA of less than 2 log10 from baseline and detectable serum HCV-RNA at week 12 predicted 99% of treatment failures. Histologic activity diminished and fibrosis stabilized in virologic responders. The 2 regimens showed similar tolerability although dose modifications for clinical and biological events were more frequent with peginterferon. Eleven cases of pancreatitis or symptomatic hyperlactatemia were observed, all in patients receiving didanosine-containing antiretroviral regimens. In combination with ribavirin, treatment with peginterferon alfa-2b is more effective than standard interferon alfa-2b for HCV infection in HIV-infected patients.

MeSH Terms
Adult Antiviral Agents/therapeutic use Drug Carriers Drug Therapy, Combination Female HIV Infections/blood,complications Hepacivirus/genetics Hepatitis C, Chronic/blood,complications,drug therapy Humans Interferon alpha-2 Interferon-alpha/therapeutic use Male Polyethylene Glycols Prospective Studies Recombinant Proteins Ribavirin/therapeutic use Viral Load
Chemicals
Antiviral Agents Drug Carriers Interferon alpha-2 Interferon-alpha Recombinant Proteins Polyethylene Glycols Ribavirin peginterferon alfa-2b
Authors & Affiliations
15 authors, click to expand affiliations / ORCID
Carrat Fabrice
Groupe Hospitalier Universitaire Est, Université Paris 6, INSERM U444, Paris, France.
Bani-Sadr Firouzé
Pol Stanislas
Rosenthal Eric
Lunel-Fabiani Françoise
Benzekri Asmae
Morand Patrice
Goujard Cécile
Pialoux Gilles
Piroth Lionel
Salmon-Céron Dominique
Degott Claude
Cacoub Patrice
Perronne Christian
ANRS HCO2 RIBAVIC Study Team
Article Info
Journal
JAMA
Abbr.
JAMA
ISSN
1538-3598
Published
2004-12-15
Pages
2839-48
Language
English
Region
United States
NLM ID
7501160
Subset
IM
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