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J Gastroenterol Hepatol ; 20(11): 1721-5, 2005 Nov.
Article in English | MEDLINE | ID: mdl-16246192

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.


Subject(s)
Antiviral Agents/therapeutic use , Hepatitis B Antibodies/blood , Hepatitis B e Antigens/immunology , Hepatitis B, Chronic/drug therapy , Interferons/therapeutic use , Lamivudine/administration & dosage , Reverse Transcriptase Inhibitors/administration & dosage , Adult , Aged , Drug Administration Schedule , Drug Resistance, Viral/genetics , Drug Therapy, Combination , Female , Hepatitis B virus/genetics , Hepatitis B, Chronic/immunology , Hepatitis B, Chronic/virology , Humans , Lamivudine/therapeutic use , Male , Middle Aged , Mutation , Recurrence , Reverse Transcriptase Inhibitors/therapeutic use , Time Factors
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