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

Erik Buster, Bettina Hansen, GKK Lau, T Piratvisuth, S Zeuzem, Ewout Steyerberg, HLA Janssen

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BACKGROUND & AIMS: Therapy with pegylated interferon (PEG-IFN)-alfa results in sustained response in a minority of patients with chronic hepatitis B virus (HBV) infection and has considerable side effects. We analyzed data from the 2 largest global trials of hepatitis B e antigen (HBeAg)-positive patients with chronic hepatitis B to determine which are most likely to respond to PEG-IFN-alfa therapy. METHODS: The study included 542 patients treated with PEG-IFN-alfa-2a (180 mu g/wk, 48 wk) and 266 patients treated with PEG-IFN-alfa-2b (100 mu g/wk, 52 wk). Eighty-seven patients were excluded, leaving 721 patients for analysis. A sustained response was defined as HBeAg loss and HBV-DNA level less than 2.0 X 10(3) IU/mL 6 months after treatment. Logistic regression analysis was used to identify predictors of sustained response and a multivariable model was constructed. RESULTS: HBV genotype, high levels of alanine aminotransferase (ALT; >= 2 X upper limit of normal), tow levels of HBV DNA (<2.0 X 10(8) IU/mL), female sex, older age, and absence of previous IFN therapy predicted a sustained response. Genotype A patients with high ALT and/or low HBV-DNA levels had a high predicted probability (>30%) of a sustained response. The strongest predictors of response were a high level of ALT in genotype B patients and a low level of HBV DNA in genotype C patients. Genotype D patients had a low chance of sustained response, irrespective of ALT or HBV-DNA levels. CONCLUSIONS: The best candidates for a sustained response to PEG-IFN-alfa are genotype A patients with high levels of ALT or low levels of HBV DNA, and genotypes B and C patients who have both high levels of ALT and low HBV DNA. Genotype D patients have a low chance of sustained response.
Original languageUndefined/Unknown
Pages (from-to)2002-2009
Number of pages8
Issue number6
Publication statusPublished - 2009

Research programs

  • EMC MM-04-20-02-A
  • EMC NIHES-01-66-01
  • EMC NIHES-02-65-01

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