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首页> 外文期刊>The Journal of Antimicrobial Chemotherapy >Sequential treatment with lamivudine and interferon-alpha monotherapies in hepatitis B e antigen-negative Chinese patients and its suppression of lamivudine-resistant mutations.
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Sequential treatment with lamivudine and interferon-alpha monotherapies in hepatitis B e antigen-negative Chinese patients and its suppression of lamivudine-resistant mutations.

机译:拉米夫定和干扰素-α单一疗法对乙型肝炎e抗原阴性的中国患者的序贯治疗及其对拉米夫定耐药性突变的抑制作用。

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OBJECTIVES: To assess the efficacy of sequential treatment with lamivudine and interferon-alpha monotherapies in Chinese patients with hepatitis B e antigen (HBeAg)-negative chronic hepatitis B. METHODS: One hundred and sixty-two patients with HBeAg-negative chronic hepatitis B were included in this study. Ninety-eight were treated with lamivudine alone (100 mg per day) for 48 weeks (group B). Sixty-four were treated with lamivudine alone (100 mg per day) for 20 weeks, then combined with interferon-alpha-2b (5 million units three times per week) for 4 weeks and then treated for another 24 weeks with interferon-alpha-2b alone (5 million units three times per week) (group A). All patients were followed for an additional 24 weeks. RESULTS: After 48 weeks of treatment, the percentage of patients with normalization of alanine aminotransferase (ALT) levels or hepatitis B virus (HBV) DNA levels below 1000 copies/mL was not significantly different between the lamivudine monotherapy group (55.10% and 55.10%, respectively) and the sequential treatment group (59.36% and 56.25%, respectively). The percentage of patients with normalized ALT levels was significantly higher in group A (53%) than in group B (36%) at week 72 (P<0.05). The percentage of patients with lamivudine-resistant mutations was significantly higher with lamivudine monotherapy (22.45%) than with sequential therapy (P<0.05). CONCLUSIONS: Sequential treatment of chronic hepatitis B with lamivudine and interferon-alpha monotherapies is as effective as lamivudine-alone treatment in Chinese patients. However, sequential treatment can significantly suppress the emergence of lamivudine-resistant mutations.
机译:目的:评估拉米夫定和干扰素-α单一疗法相继治疗对中国乙型肝炎e抗原(HBeAg)阴性的慢性乙型肝炎的疗效。方法:162例HBeAg阴性的慢性乙型肝炎患者包括在这项研究中。 98名患者单独接受拉米夫定治疗(每天100 mg)48周(B组)。 64名患者单独接受拉米夫定治疗(每天100 mg)20周,然后与α-干扰素2b组合(每周3百万次,五百万次)治疗4周,然后再用α-干扰素治疗24周。单独2b(每周3次500万单位)(A组)。所有患者均再随访24周。结果:治疗48周后,拉​​米夫定单药治疗组中丙氨酸氨基转移酶(ALT)水平或乙型肝炎病毒(HBV)DNA水平恢复正常的患者百分比在拉米夫定单药治疗组之间无显着差异(55.10%和55.10% )和序贯治疗组(分别为59.36%和56.25%)。在第72周,ALT水平正常的患者百分比在A组(53%)显着高于B组(36%)(P <0.05)。拉米夫定单药治疗具有拉米夫定耐药突变的患者百分比(22.45%)显着高于顺序治疗(P <0.05)。结论:拉米夫定和干扰素-α单药序贯治疗慢性乙型肝炎与单用拉米夫定单独治疗在中国患者中一样有效。但是,序贯治疗可以显着抑制拉米夫定耐药突变的出现。

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