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依曲韦林

Etravirine.

作者信息

Deeks Emma D, Keating Gillian M

机构信息

Wolters Kluwer Health, Adis, Auckland, New Zealand.

出版信息

Drugs. 2008;68(16):2357-72. doi: 10.2165/0003495-200868160-00007.

Abstract

Etravirine is a next-generation non-nucleoside reverse transcriptase inhibitor (NNRTI) that demonstrates potent in vitro activity against wild-type strains of HIV type 1 (HIV-1), as well as against numerous strains resistant to available NNRTIs. Furthermore, the potential for resistance to etravirine developing appears to be lower than for first-generation NNRTIs. In treatment-experienced patients infected with HIV-1 with NNRTI resistance, HIV-1 RNA levels of <50 copies/mL (primary endpoint) and <400 copies/mL were achieved by a significantly greater proportion of patients receiving etravirine 200 mg twice daily plus background therapy (BT) than placebo plus BT, according to the planned pooled and individual 24-week analyses of two large, well designed, continuing phase III trials (DUET-1 and DUET-2). In the pooled 24-week analysis, patients receiving etravirine plus BT achieved a significantly greater mean reduction in viral load from baseline and a significantly greater mean increase in CD4+ cell counts from baseline than patients receiving placebo plus BT. The pooled and individual findings of the DUET studies at 48 weeks indicate that the efficacy of etravirine is maintained with regard to these endpoints. In the DUET studies, etravirine was generally well tolerated in treatment-experienced patients infected with HIV-1, with a tolerability profile generally similar to that of placebo. Adverse events were mostly of mild or moderate severity.

摘要

依曲韦林是一种新一代非核苷类逆转录酶抑制剂(NNRTI),它在体外对1型人类免疫缺陷病毒(HIV-1)野生型毒株以及对多种现有NNRTIs耐药的毒株均显示出强效活性。此外,依曲韦林产生耐药的可能性似乎低于第一代NNRTIs。根据两项大型、设计良好的持续III期试验(DUET-1和DUET-2)的计划汇总分析和个体24周分析,在接受过治疗且对NNRTIs耐药的HIV-1感染患者中,与接受安慰剂加背景治疗(BT)相比,接受每日两次200 mg依曲韦林加BT的患者中,有显著更高比例的患者实现了HIV-1 RNA水平<50拷贝/毫升(主要终点)和<400拷贝/毫升。在汇总的24周分析中,接受依曲韦林加BT的患者与接受安慰剂加BT的患者相比,从基线开始病毒载量的平均降低幅度显著更大,CD4 +细胞计数从基线开始的平均增加幅度也显著更大。DUET研究在48周时的汇总和个体研究结果表明,依曲韦林在这些终点方面的疗效得以维持。在DUET研究中,依曲韦林在接受过治疗的HIV-1感染患者中总体耐受性良好,耐受性特征通常与安慰剂相似。不良事件大多为轻度或中度严重程度。

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