拉米夫定治疗乙型肝炎e抗原阴性慢性肝病疗效观察

In du Jeong, Neung Hwa Park, Byung Chul Kim, Jee Hyun Park, Kwang Won Seo, Dae-Hyun Kim, Kwang Ro Joo, Do Ha Kim
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引用次数: 0

摘要

背景/目的:拉米夫定治疗可有效抑制hbeag阴性慢性肝病患者的HBV复制。然而,持续缓解率似乎特别差,因为绝大多数患者在停止治疗后很快复发。本研究的目的是评估拉米夫定对hbeag阴性慢性肝病患者的疗效、突破率和缓解后停药的复发率。方法:对59例接受拉米夫定治疗至少6个月的hbeag阴性慢性肝病患者进行研究。平均治疗时间为14个月。完全缓解定义为bDNA检测不到血清HBV DNA和ALT水平正常化。一旦观察到HBV DNA消失和ALT正常化,拉米夫定治疗至少再持续两个月。停止治疗后平均随访6(1-22)个月。结果:56例患者HBV DNA未检出。3个月和5个月的累积HBV DNA损失率分别为90%和95%。52例患者ALT恢复正常。6个月和10个月ALT累计正常化率分别为78%和86%。在52例患者中观察到完全缓解。10个月和18个月的累计完全缓解率分别为80%和88%。完全缓解的预测因素仅是拉米夫定治疗的持续时间。5例(8.5%)出现病毒学突破。34例患者在7.7(2-15)个月的额外治疗后停止服用拉米夫定。其中17例(50%)复发。3个月、6个月和10个月的累计复发率分别为24%、47%和66%。复发的唯一预测因素是缓解后额外拉米夫定治疗的持续时间。结论:拉米夫定是治疗HBeAg阴性慢性肝病的有效药物。然而,复发通常在拉米夫定停药后观察到。我们的研究结果表明,为了降低hbeag阴性慢性肝病患者的高复发率,长期拉米夫定治疗是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Efficacy of lamivudine in patients with hepatitis B e antigen-negative chronic liver diseases].

Background/aims: Lamivudine therapy is effective in inhibiting HBV replications in patients with HBeAg-negative chronic liver disease. However, the sustained response rate appears to be particularly poor, because the vast majority of patients relapse soon after cessation of therapy. The aim of this study was to evaluate the efficacy of lamivudine, the breakthrough rate, and the relapse rate of discontinuing therapy after response in patients with HBeAg-negative chronic liver disease.

Methods: Fifty-nine patients with HBeAg-negative chronic liver disease who have received lamivudine for at least 6 months, were studied. The mean duration of treatment was 14 months. Complete response was defined as undetectable serum HBV DNA by bDNA and normalization of ALT levels. Once HBV DNA disappearance and ALT normalization were observed, lamivudine therapy was continued for at least two additional months. The mean follow-up after cessation of treatment was 6 (1-22) months.

Results: Fifty-six patients were undetectable HBV DNA. The cumulative HBV DNA loss rates at 3 months and 5 months were 90% and 95%, respectively. The ALT normalization was observed in 52 patients. The cumulative ALT normalization rates at 6 months and 10 months were 78% and 86%, respectively. The complete response was observed in 52 patients. The cumulative rates of complete response at 10 months and 18 months were 80% and 88%, respectively. A predictive factor for complete response was only the duration of lamivudine treatment. Virological breakthrough was observed in 5 (8.5%). Thirty-four patients stopped taking lamivudine after 7.7 (2-15) months of the additional therapy. Seventeen of those patients (50%) experienced relapse. The cumulative relapse rates at 3 months, 6 months and 10 months were 24%, 47%, and 66%, respectively. The only predictive factor for relapse was the duration of additional lamivudine treatment after response.

Conclusions: Lamivudine was an effective treatment of HBeAg negative chronic liver disease. Relapse, however, was usually observed after cessation of lamivudine. Our results showed that long-term lamivudine therapy is required in order to decrease the high relapse rates in patients with HBeAg-negative chronic liver disease.

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