Gastroenterology
Volume 129, Issue 2 , Pages 522-527, August 2005

Peginterferon-α-2a (40KD) and Ribavirin for 16 or 24 Weeks in Patients With Genotype 2 or 3 Chronic Hepatitis C

Data of the present study were presented in part at the 55th Annual Meeting of the American Association for the Study of Liver Diseases, October 29–November 2, 2004, Boston, Massachusetts.

  • Michael von Wagner

      Affiliations

    • Universitätsklinikum des Saarlandes, Homburg/Saar, Germany
  • ,
  • Miriam Huber

      Affiliations

    • Klinikum der Johann Wolfgang Goethe-Universität, Frankfurt a. M., Germany
  • ,
  • Thomas Berg

      Affiliations

    • Charité, Campus Virchow-Klinikum, Berlin, Germany
  • ,
  • Holger Hinrichsen

      Affiliations

    • Klinikum der Christian-Albrecht-Universität, Kiel, Germany
  • ,
  • Jens Rasenack

      Affiliations

    • Medizinische Universitätsklinik Freiburg, Freiburg, Germany
  • ,
  • Tobias Heintges

      Affiliations

    • Klinikum der Heinrich-Heine-Universität, Düsseldorf, Germany
  • ,
  • Alexandra Bergk

      Affiliations

    • Charité, Campus Virchow-Klinikum, Berlin, Germany
  • ,
  • Christine Bernsmeier

      Affiliations

    • Klinikum der Christian-Albrecht-Universität, Kiel, Germany
  • ,
  • Dieter Häussinger

      Affiliations

    • Klinikum der Heinrich-Heine-Universität, Düsseldorf, Germany
  • ,
  • Eva Herrmann

      Affiliations

    • Universitätsklinikum des Saarlandes, Homburg/Saar, Germany
  • ,
  • Stefan Zeuzem

      Affiliations

    • Universitätsklinikum des Saarlandes, Homburg/Saar, Germany
    • Klinikum der Johann Wolfgang Goethe-Universität, Frankfurt a. M., Germany
    • Corresponding Author InformationAddress requests for reprints to: Stefan Zeuzem, MD, Prof, Klinik für Innere Medizin II, Universitätklinikum des Saarlandes, Kirrbergerstrasse, 66421 Homburg/Saar, Germany.fax: (49) 6841-16-23267.

Received 20 January 2005; accepted 20 April 2005.

Background & Aims: Standard therapy of patients with chronic hepatitis C virus (HCV) infected with HCV genotype-2 or -3 is the combination of pegylated interferon-α and ribavirin for 24 weeks. Whether shorter treatment durations are possible for these patients without compromising sustained virologic response rates is unknown. Methods: Patients chronically infected with HCV-2 (n = 39), HCV-2/3 (n = 1), or HCV-3 (n = 113) were treated with peginterferon-α-2a (180 μg/wk) plus ribavirin 800–1200 mg/day. HCV RNA was quantitatively assessed after 4 weeks. Patients with a rapid virologic response (HCV RNA below 600 IU/mL) were randomized for a total treatment duration of 16 (group A) or 24 weeks (group B). All patients with HCV RNA ≥600 IU/mL at week 4 (group C) were treated for 24 weeks. End-of-treatment and sustained virologic response were assessed by qualitative RT-PCR (sensitivity 50 IU/mL). Results: Only 11 of 153 patients (7%) were allocated to group C. End-of-treatment and sustained virologic response rates were 94% and 82%, (group A), 85% and 80% (group B), and 73% and 36% (group C), respectively. In patients infected with genotype HCV-3 and high viral load (>800,000 IU/mL), a significant lower sustained virologic response rate was found than in patients infected with HCV-3 and a viral load lower or equal to 800,000 IU/mL (59% vs 85%, respectively; P = .003). Conclusions: In HCV-2 and -3 (low viral load)-infected patients who have a rapid virologic response, treatment for 16 weeks with peginterferon-α-2a and ribavirin is sufficient. In patients infected by HCV-3 (high viral load), longer treatment may be necessary.

Abbreviation used in this paper:  HCV, hepatitis C virus

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 Supported by an unrestricted research grant from Hoffmann-La Roche, Grenzach, Germany, and by the German Hepatitis Network of Competence (Hep-Net).In addition to the authors, the following investigators were involved in the present study: Klaus Freivogel, Analytica International, Lörrach, Germany, and Andreas Erhardt, Klinikum der Heinrich-Heine-Universität, Düsseldorf, Germany.

PII: S0016-5085(05)00878-4

doi:10.1053/j.gastro.2005.05.008

Gastroenterology
Volume 129, Issue 2 , Pages 522-527, August 2005