[Efficacy of lamivudine re-treatment and relapse patterns after initial lamivudine treatment for chronic hepatitis B infection].

Jong Ho Park, Neung Hwa Park, Jung Woo Shin, Sung-Jo Bang, Dae-Hyun Kim, Kwang Ro Joo, Do Ha Kim
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Abstract

Background/aims: The post-treatment relapse patterns and efficacy of lamivudine re-treatment for relapsed patients have not been clarified. The aims of this study were to evaluate the relapse patterns after discontinuing therapy and the effects of lamivudine re-treatment for relapsed patients after HBeAg seroconversion.

Methods: Therapy was discontinued after HBeAg seroconversion in 121 patients. Sixty-six patients were relapsed and included in this study. The duration of lamivudine re-treatment therapy was from 6-35 (mean: 16) months. Post-retreatment monitoring continued for 1-40 (mean: 8.9) months.

Results: Among the relapsed 66 patients, 50 (75.8%) had HBeAg reappearance while 16 (24.2%) remained HBeAg negative and anti-HBe positive. The cumulative relapse rates at 3, 6, 12 and 24 months were 27%, 47%, 60% and 66%, respectively. Forty-two relapsers received lamivudine re-treatment. Among them, 33 were HBeAg positive and 9 were HBeAg negative and anti-HBe positive, Response was achieved in 31 of the 42 patients (73.8%). The cumulative response rates at 6, 9 and 12 months were 62%, 69% and 72%, respectively. Six patients (14.3%) developed viral breakthrough. All patients were HBeAg positive chronic hepatitis B. The duration of lamivudine re-treatment was the only predictable factor for response of lamivudine re-treatment. Therapy was discontinued after response in 21 patients. Eleven patients were relapsed, including 6 who were HBeAg positive and 5 who were HBeAg negative. Predictive factors for post-retreatment relapse were age and the duration of additional lamivudine therapy after response.

Conclusions: The response rate of lamivudine re-treatment was significantly higher than in initial lamivudine treatments. The breakthrough and relapse rates, however, were similar in both initial and retreated lamivudine therapy.

[拉米夫定治疗慢性乙型肝炎感染后再治疗的疗效及复发模式]。
背景/目的:拉米夫定再治疗复发患者的治疗后复发模式和疗效尚未明确。本研究的目的是评估停止治疗后的复发模式和拉米夫定再治疗对HBeAg血清转化后复发患者的影响。方法:121例患者在HBeAg血清转化后停止治疗。66例复发患者纳入本研究。拉米夫定再治疗持续时间6 ~ 35个月(平均16个月)。再治疗后持续监测1-40个月(平均8.9个月)。结果:66例复发患者中,HBeAg复发50例(75.8%),HBeAg阴性和抗- hbe阳性16例(24.2%)。3、6、12、24个月的累计复发率分别为27%、47%、60%、66%。42例复发患者再次接受拉米夫定治疗。其中HBeAg阳性33例,HBeAg阴性和抗- hbe阳性9例,42例患者中有31例(73.8%)获得缓解。6个月、9个月和12个月的累积缓解率分别为62%、69%和72%。6例(14.3%)出现病毒突破。所有患者均为慢性乙型肝炎HBeAg阳性,拉米夫定再治疗的持续时间是拉米夫定再治疗疗效的唯一可预测因素。21例患者缓解后停止治疗。11例患者复发,其中HBeAg阳性6例,HBeAg阴性5例。再治疗后复发的预测因素是年龄和缓解后额外拉米夫定治疗的持续时间。结论:拉米夫定再治疗有效率明显高于拉米夫定初始治疗。然而,在最初和退却拉米夫定治疗中,突破率和复发率相似。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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