Interferon-ribavirin for chronic hepatitis C with and without cirrhosis: Analysis of individual patient data of six controlled trials

被引:128
作者
Schalm, SW
Weiland, O
Hansen, BE
Milella, M
Lai, FY
Hollander, A
Michielsen, PP
Bellobuono, A
Chemello, L
Pastore, G
Chen, DS
Brouwer, JT
机构
[1] Erasme Univ Hosp, Dept Hepatogastroenterol & Biostat, Rotterdam, Netherlands
[2] Huddinge Hosp, Karolinska Inst, Dept Infect Dis, S-14186 Huddinge, Sweden
[3] Univ Bari, Inst Infect Dis, Bari, Italy
[4] Natl Taiwan Univ Hosp, Dept Internal Med, Taipei 100, Taiwan
[5] Univ Antwerp Hosp, Dept Gastroenterol, Antwerp, Belgium
[6] Osped Niguarda Ca Granda, Crespi Div Med, Milan, Italy
[7] Osped Niguarda Ca Granda, Ctr Liver Dis, Milan, Italy
[8] Univ Padua, Dept Med, Padua, Italy
关键词
D O I
10.1053/gast.1999.0029900408
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: The aim of this study was to compare interferon (IFN)-ribavirin combination therapy with IFN monotherapy in chronic hepatitis C with particular focus on its efficacy in cirrhosis. Methods: A multivariate analysis of individual patient data of all randomized controlled trials using an IFN-ribavirin arm, reported between 1991 and March 1998, was performed. Centers included 1 Asian and 5 European university-based referral centers for liver disease. A total of 197 patients with chronic hepatitis C received IFN-alpha (3 MU three times weekly) and ribavirin (1-1.2 g daily) for 6 months, and 147 patients received IFN-alpha (3 MU three times weekly) for 6 months. Patients were characterized according to previous IFN therapy, presence of cirrhosis, and genotype 1. Efficacy of therapy was evaluated by assessing the sustained response rate by logistic regression analysis. Results: Patients without cirrhosis treated with IFN-ribavirin had a significantly higher sustained response rate than those treated with IFN, approximately 3-fold for previously untreated patients (IFN-ribavirin: genotype 1, 33%; genotype 2/3, 65%; IFN: genotype 1, 8%; genotype 2/3, 24%). In cirrhosis, sustained response rates with IFN-ribavirin (previously untreated: genotype 1, 7%; genotype 2/3, 24%) were also significantly higher than those with IFN (previously untreated: genotype 1, 1%; genotype 2/3, 5%). Clinical relevant superiority of combination therapy over IFN monotherapy was also observed for relapse; the same trend was observed for nonresponders. Tolerance for IFN-ribavirin was similar for patients with or without cirrhosis. Conclusions: Combination with ribavirin significantly enhances the sustained response rate of IFN therapy in major patient types (cirrhosis, genotype 1) with chronic hepatitis C. Thus, IFN-ribavirin combination is likely to become the antiviral therapy of choice for cirrhosis caused by hepatitis C.
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页码:408 / 413
页数:6
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