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核苷(酸)类似物治疗失败的乙型肝炎病毒单感染患者使用替诺福韦单药治疗的长期疗效。

Long-term efficacy of tenofovir monotherapy for hepatitis B virus-monoinfected patients after failure of nucleoside/nucleotide analogues.

机构信息

Medizinische Klinik m. S. Hepatologie und Gastroenterologie Charité, Campus Virchow-Klinikum, Universitätsmedizin Berlin, Germany.

出版信息

Hepatology. 2010 Jan;51(1):73-80. doi: 10.1002/hep.23246.

Abstract

UNLABELLED

Tenofovir disoproxil fumarate (TDF) has demonstrated high antiviral efficacy in treatment-naive patients with chronic hepatitis B virus (HBV) infection but experience in nucleoside/nucleotide analogue (NA)-experienced patients is limited. In this retrospective multicenter study we therefore assessed the long-term efficacy of TDF monotherapy in patients with prior failure or resistance to different NA treatments. Criteria for inclusion were HBV DNA levels >4.0 log(10) copies/mL at the start and a minimum period of TDF therapy for at least 6 months. In all, 131 patients (mean age 42 +/- 12 years, 95 male, 65% hepatitis B e antigen [HBeAg]-positive) were eligible. Pretreatment consisted of either monotherapy with lamivudine (LAM; n = 18), adefovir (ADV; n = 8), and sequential LAM-ADV therapy (n = 73), or add-on combination therapy with both drugs (n = 29). Three patients had failed entecavir therapy. Resistance analysis in 113 of the 131 patients revealed genotypic LAM and ADV resistance in 62% and 19% of patients, respectively. The mean HBV DNA level at TDF baseline was 7.6 +/- 1.5 log(10) copies/mL. The overall cumulative proportion of patients achieving HBV DNA levels <400 copies/mL was 79% after a mean treatment duration of 23 months (range, 6-60). Although LAM resistance did not influence the antiviral efficacy of TDF, the presence of ADV resistance impaired TDF efficacy (100% versus 52% probability of HBV DNA <400 copies/mL, respectively). However, virologic breakthrough was not observed in any of the patients during the entire observation period. Loss of HBeAg occurred in 24% of patients and HBsAg loss occurred in 3%. No significant adverse events were noticed during TDF monotherapy.

CONCLUSION

TDF monotherapy induced a potent and long-lasting antiviral response in NA-experienced patients with previous treatment failure. Our data may have implications for current add-on strategies.

摘要

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替诺福韦二吡呋酯(TDF)在初治慢性乙型肝炎病毒(HBV)感染患者中显示出很高的抗病毒疗效,但在核苷(酸)类似物(NA)治疗失败的患者中的经验有限。因此,在这项回顾性多中心研究中,我们评估了 TDF 单药治疗在先前对不同 NA 治疗失败或耐药的患者中的长期疗效。纳入标准为治疗开始时 HBV DNA 水平>4.0 log(10)拷贝/ml,TDF 治疗时间至少 6 个月。共有 131 例患者(平均年龄 42 +/- 12 岁,95 例男性,65%乙型肝炎 e 抗原[HBeAg]-阳性)符合条件。治疗前包括拉米夫定(LAM;n = 18)、阿德福韦(ADV;n = 8)或 LAM-ADV 序贯治疗(n = 73)单药治疗,或两种药物联合加用治疗(n = 29)。3 例患者恩替卡韦治疗失败。对 131 例患者中的 113 例进行耐药性分析,分别有 62%和 19%的患者存在基因型 LAM 和 ADV 耐药。TDF 基线时 HBV DNA 平均水平为 7.6 +/- 1.5 log(10)拷贝/ml。在平均治疗 23 个月(范围 6-60)后,所有患者中达到 HBV DNA 水平<400 拷贝/ml 的累积比例为 79%。尽管 LAM 耐药不影响 TDF 的抗病毒疗效,但 ADV 耐药会损害 TDF 的疗效(HBV DNA <400 拷贝/ml 的概率分别为 100%和 52%)。然而,在整个观察期间,没有患者发生病毒学突破。24%的患者发生 HBeAg 丢失,3%的患者发生 HBsAg 丢失。在 TDF 单药治疗期间未发现明显的不良事件。

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