Interferon/long-term lamivudine combination therapy in anti-HBe positive chronic hepatitis B patients
Article first published online: 12 OCT 2005
DOI: 10.1111/j.1440-1746.2005.04029.x
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How to Cite
NIKOLAIDIS, N. L., GIOULEME, O. I., TZIOMALOS, K. A., SAVERIADIS, A. S., GRAMMATIKOS, N., DOUKELIS, P., VOUTSAS, A. D., VASSILIADIS, T., PATSIAOURA, K., ORFANOU-KOUMERKERIDOU, E., BALASKA, A. and EUGENIDIS, N. P. (2005), Interferon/long-term lamivudine combination therapy in anti-HBe positive chronic hepatitis B patients. Journal of Gastroenterology and Hepatology, 20: 1721–1725. doi: 10.1111/j.1440-1746.2005.04029.x
Publication History
- Issue published online: 12 OCT 2005
- Article first published online: 12 OCT 2005
- Accepted for publication 18 November 2004.
- Abstract
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Keywords:
- anti-HBe positive chronic hepatitis B;
- combination therapy;
- lamivudine resistance
Abstract
Background: Monotherapy with a single antiviral agent is insufficient in controlling hepatitis B virus infection in the majority of patients with anti-HBe positive chronic hepatitis B. Interferon/long-term lamivudine combination therapy was evaluated to determine if this strategy would improve treatment efficacy and reduce the emergence of lamivudine resistance.
Methods: In total, 36 consecutive anti-HBe positive patients were treated with interferon (3 MU subcutaneously three times weekly) and lamivudine (100 mg orally once a day) for 12 months. After completion of the combined treatment, all patients continued to receive lamivudine monotherapy indefinitely.
Results: Overall, 35 patients (97%) showed virological response at 12 months. Four patients (11%) cleared HBsAg and developed anti-HBs. During the follow-up time, after the discontinuation of interferon, of 30 ± 12 months (range: 7–57 months), 13 patients (36%) exhibited breakthrough infection. The cumulative rates of breakthrough infection at the end of 1, 2, 3 and 4 years of treatment were 0%, 14%, 32%, and 59%, respectively.
Conclusions: Combination therapy appears to be effective and may also delay the selection of lamivudine-resistant variants. However, controlled trials are definitely warranted to clarify the potential benefits of combination antiviral treatment over monotherapy.

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