Gastroenterology
Volume 137, Issue 6 , Pages 2002-2009 , December 2009

Factors That Predict Response of Patients With Hepatitis B e Antigen–Positive Chronic Hepatitis B to Peginterferon-Alfa

  • Erik H.C.J. Buster

      Affiliations

    • Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands
  • ,
  • Bettina E. Hansen

      Affiliations

    • Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands
    • Department of Epidemiology and Biostatistics, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands
  • ,
  • George K.K. Lau

      Affiliations

    • Department of Medicine, Queen Mary Hospital, University of Hong Kong, Hong Kong SAR, China
  • ,
  • Teerha Piratvisuth

      Affiliations

    • Department of Medicine, Songklanakarin Hospital, Songkla, Thailand
  • ,
  • Stefan Zeuzem

      Affiliations

    • Medizinische Klinik I, Klinikum der Johann Wolfgang Goethe-Universität, Frankfurt am Main, Germany
  • ,
  • Ewout W. Steyerberg

      Affiliations

    • Department of Public Health, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands
  • ,
  • Harry L.A. Janssen

      Affiliations

    • Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands
    • Corresponding Author InformationReprint requests Address requests for reprints to: Harry L. A. Janssen, MD, PhD, Department of Gastroenterology and Hepatology, Erasmus MC, University Medical Center Rotterdam's Gravendijkwal 230, Room Ha204, 3015 CE Rotterdam, The Netherlands. fax: 0031-10-4365916

Received 25 March 2009 ,Accepted 26 August 2009.

  • Image Result

    Distribution of predicted probabilities of sustained response in patients with HBV genotypes A–D. Boxplots show the distribution of the predicted probabilities of sustained response, defined as HBeAg

    Distribution of predicted probabilities of sustained response in patients with HBV genotypes A–D. Boxplots show the distribution of the predicted probabilities of sustained response, defined as HBeAg loss and HBV DNA less than 10,000 copies/mL at 6 months posttreatment, in patients with genotype A (n = 115), B (n = 166), C (n = 333), or D (n = 107).

  • Image Result
    PEG-IFN HBV treatment index. These nomograms can be used to obtain a patient-tailored predicted probability of sustained response in IFN-naive patients with genotypes A–D based on ALT level, HBV-DNA l

    PEG-IFN HBV treatment index. These nomograms can be used to obtain a patient-tailored predicted probability of sustained response in IFN-naive patients with genotypes A–D based on ALT level, HBV-DNA level, sex, and age. The probability of sustained response is calculated by drawing a vertical line to the top points axis for each of the 4 variables ALT, HBV DNA, age, and sex. The points for each variable then are summed and located on the total points axis, and a vertical line is projected from the total points axis to the bottom scale to get the predicted probability of sustained response. For example, a genotype C–infected woman (62 points), age 25 (67 points), with serum ALT level of 2.7 × ULN (25 points), and serum HBV-DNA level of 9.2 log10 copies/mL (40 points) has a total score of 194 points, which converts to a probability of sustained response of 37%.

  • Image Result
    Flowcharts to easily obtain average predicted probabilities of sustained response in patients infected with HBV genotypes A–D. These flowcharts show the average predicted probability of sustained resp

    Flowcharts to easily obtain average predicted probabilities of sustained response in patients infected with HBV genotypes A–D. These flowcharts show the average predicted probability of sustained response depending on HBV genotype, ALT level (> or <2 × ULN), and HBV-DNA level (> or <9 log10 copies/mL). For a precise estimate of the probability of sustained response in an individual patient, the nomograms in Figure 2 can be used.

 Funding The Peginterferon Alfa-2a HBeAg-Positive Chronic Hepatitis B Study was supported by a research grant from Roche (Basel, Switzerland). The HBV99-01 study was organized and sponsored by the Foundation for Liver Research (SLO), Rotterdam, The Netherlands. Financial support and study medication for the HBV99-01 study was provided by Schering-Plough International (Kenilworth, NJ) and GlaxoSmithKline (Greenford, UK).

 Conflicts of interest These authors disclose the following: Erik H.C.J. Buster received speaker's honoraria from Novartis and Roche; George K. Lau consulted for Roche and Novartis; Teerha Piratvisuth consulted for GlaxoSmithKline, Novartis, and Schering-Plough, and received research support from Roche and Bristol-Myers Squibb; Stefan Zeuzem was a consultant for Bristol-Myers Squibb, Gilead, Novartis, Roche, and Schering-Plough, was on the speaker's bureau for Gilead and Novartis, and received research support from Roche; Harry L. A. Janssen received research support from Bristol-Myers Squibb, Gilead, Novartis, Roche, Schering-Plough, and was a consultant for Bristol-Myers Squibb, Novartis, and Roche. The remaining authors disclose no conflicts. Potential investigator conflicts of interest have not been disclosed to study participants.

PII: S0016-5085(09)01551-0

doi: 10.1053/j.gastro.2009.08.061

Gastroenterology
Volume 137, Issue 6 , Pages 2002-2009 , December 2009