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Am J Gastroenterol ; 101(11): 2523-9, 2006 Nov.
Article in English | MEDLINE | ID: mdl-17029610

ABSTRACT

OBJECTIVES: Antiviral therapy leads to HBeAg seroconversion in 10-40% of the patients with HBeAg-positive chronic hepatitis B. Nonresponse may result in progression of liver disease and increased risk of hepatocellular carcinoma. As part of a global randomized controlled trial we investigated the efficacy (i.e., loss of HBeAg at the end of follow-up) of peginterferon alfa-2b (Peg-IFN alpha2b) in patients who failed to respond to previous courses of standard interferon (IFN) or lamivudine. METHODS: We analyzed a total of 76 previous nonresponders: 37 were nonresponders to standard IFN, 17 were nonresponders to lamivudine, and 22 were nonresponders to both therapies. All patients received a 52-wks course of 100 microg Peg-IFN alpha2b weekly combined with either 100 mg lamivudine daily or a placebo. After therapy patients were followed for 26 wks. RESULTS: Thirteen (35%) nonresponders to previous IFN, five (29%) nonresponders to previous lamivudine, and four (22%) nonresponders to both IFN and lamivudine responded to treatment with Peg-IFN alpha2b. No difference in response was found for those treated with Peg-IFN alpha2b alone or in combination with lamivudine. Nonresponders to prior IFN therapy with baseline ALT (alanine aminotransferase) > 4 x ULN (upper limit of normal) responded better to Peg-IFN alpha2b than those with ALT levels

Subject(s)
Antiviral Agents/therapeutic use , Hepatitis B e Antigens/analysis , Hepatitis B, Chronic/drug therapy , Interferon-alpha/therapeutic use , Adult , Antiviral Agents/administration & dosage , Female , Humans , Interferon alpha-2 , Interferon-alpha/administration & dosage , Interferons/therapeutic use , Lamivudine/therapeutic use , Male , Polyethylene Glycols , Recombinant Proteins
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