Literature DB >> 7843696

Ability of prolonged interferon treatment to suppress relapse after cessation of therapy in patients with chronic hepatitis C: a multicenter randomized controlled trial.

A Kasahara1, N Hayashi, N Hiramatsu, M Oshita, H Hagiwara, K Katayama, M Kato, M Masuzawa, H Yoshihara, Y Kishida.   

Abstract

The aim of this study was to determine whether 12 months course of interferon alfa (IFN-alpha) therapy could improve the beneficial effect of IFN in chronic hepatitis C. Eighty-eight patients were treated with natural IFN-alpha for either 28 weeks (45 cases) or 52 weeks (43 cases). Sustained response was achieved in 15 (33.3%) of 45 cases treated for 28 weeks and in 23 (53.5%) of 43 cases treated for 52 weeks. Transient response with relapse of alanine transaminase (ALT) after completion of therapy was observed in 13 cases (28.9%) treated for 28 weeks and in 4 cases (9.3%) treated for 52 weeks. Thus, ALT relapse was suppressed by prolonged IFN treatment. No response was found in 17 cases (37.8%) treated for 28 weeks and in 16 cases (37.2%) treated for 52 weeks, indicating that approximately 38% of the patients with chronic hepatitis C were resistant to IFN therapy even with prolonged treatment. The rate of sustained response was significantly higher in patients with type 2a or 2b than in those with type 1b. Even in type 1b cases, it was higher in the 52-week treatment group than in the 28-week treatment group, and the rate of transient response was lower in the 52-week treatment group, indicating that relapse in type 1b cases was suppressed by prolonged IFN therapy. IFN therapy was not effective for patients with advanced liver fibrosis.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1995        PMID: 7843696

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  22 in total

1.  Hepatitis C virus genotypes in liver transplant recipients: impact on posttransplant recurrence, infections, response to interferon-alpha therapy and outcome.

Authors:  T Gayowski; N Singh; I R Marino; H Vargas; M Wagener; C Wannstedt; F Morelli; T Laskus; J J Fung; J Rakela; T E Starzl
Journal:  Transplantation       Date:  1997-08-15       Impact factor: 4.939

2.  Preferential virological response to interferon-alpha 2a in patients with chronic hepatitis C infected by virus genotype 3a and exhibiting a low gamma-GT/ALT ratio.

Authors:  S Mihm; H Hartmann; A Fayyazi; G Ramadori
Journal:  Dig Dis Sci       Date:  1996-06       Impact factor: 3.199

Review 3.  [Therapy of hepatitis C].

Authors:  D M Alscher; J C Bode
Journal:  Med Klin (Munich)       Date:  1997-03-15

4.  Clinical relevance of hepatitis C virus genotypes.

Authors:  P Simmonds
Journal:  Gut       Date:  1997-03       Impact factor: 23.059

5.  Short-term versus sustained response to interferon therapy: effect on histology.

Authors:  O Reichard
Journal:  Dig Dis Sci       Date:  1996-12       Impact factor: 3.199

6.  Predictors of response to interferon therapy.

Authors:  G Saracco; M Rizzetto
Journal:  Dig Dis Sci       Date:  1996-12       Impact factor: 3.199

7.  Dose increase augments response rate to interferon-alpha in chronic hepatitis C.

Authors:  P Ferenci; R Stauber; A Propst; R Fiedler; C Müller; M Gschwantler; K Schütze; C Datz; G Judmaier; W Vogel; G J Krejs; A Gangl
Journal:  Dig Dis Sci       Date:  1996-12       Impact factor: 3.199

8.  Treatment of chronic hepatitis C by interferon for longer duration than six months.

Authors:  T Poynard; V Leroy; P Mathurin; M Cohard; P Opolon; J P Zarski
Journal:  Dig Dis Sci       Date:  1996-12       Impact factor: 3.199

Review 9.  Hepatitis C virus: molecular biology and genetic variability.

Authors:  C Bréchot
Journal:  Dig Dis Sci       Date:  1996-12       Impact factor: 3.199

10.  Two years versus six months of interferon therapy for chronic hepatitis C.

Authors:  G C Farrell
Journal:  Dig Dis Sci       Date:  1996-12       Impact factor: 3.199

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