早期抗逆转录病毒治疗的病毒学结果:HPTN 052。

Q2 Medicine
HIV Clinical Trials Pub Date : 2017-05-01 Epub Date: 2017-04-07 DOI:10.1080/15284336.2017.1311056
Susan H Eshleman, Ethan A Wilson, Xinyi C Zhang, San-San Ou, Estelle Piwowar-Manning, Joseph J Eron, Marybeth McCauley, Theresa Gamble, Joel E Gallant, Mina C Hosseinipour, Nagalingeswaran Kumarasamy, James G Hakim, Ben Kalonga, Jose H Pilotto, Beatriz Grinsztejn, Sheela V Godbole, Nuntisa Chotirosniramit, Breno Riegel Santos, Emily Shava, Lisa A Mills, Ravindre Panchia, Noluthando Mwelase, Kenneth H Mayer, Ying Q Chen, Myron S Cohen, Jessica M Fogel
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引用次数: 22

摘要

HIV预防试验网络(HPTN) 052试验表明,在血清不一致的夫妇中,早期抗逆转录病毒治疗(ART)预防了93%的HIV传播事件。在抗逆转录病毒治疗开始后不久或病毒学失败后观察到一些相关感染。目的:评估在HPTN 052患者中开始ART治疗的病毒抑制时间和病毒学失败的相关因素。方法:1566名入组时病毒载量(VL) > 400拷贝/mL的参与者被纳入分析。这包括832例早期ART组(ART启动时CD4 350-550个细胞/mm3)和734例延迟ART组(204例ART启动时CD4 3;在抗逆转录病毒治疗开始时有CD4细胞的530人)。病毒抑制定义为ART启动后连续两次VLs≤400拷贝/mL;开始抗逆转录病毒治疗24周后连续两次vl > 1000拷贝/mL定义为病毒学失败。结果:总体而言,93%的参与者在12个月内实现了病毒抑制。病毒学失败的年发生率为3.6%。两个研究组的病毒学结果相似。较长的病毒抑制时间与较年轻的年龄、抗逆转录病毒治疗开始时较高的VL和地区(非洲与亚洲)相关。病毒学失败与年龄较小、受教育程度较低和3个月后缺乏抑制密切相关;抗逆转录病毒治疗开始时的低VL和高CD4也与病毒学失败有关。结论:确定了几个临床和人口统计学因素与较长的病毒抑制时间和病毒学失败相关。认识到这些因素可能有助于优化抗逆转录病毒治疗和预防。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Virologic outcomes in early antiretroviral treatment: HPTN 052.

Virologic outcomes in early antiretroviral treatment: HPTN 052.

Virologic outcomes in early antiretroviral treatment: HPTN 052.

Introduction: The HIV Prevention Trials Network (HPTN) 052 trial demonstrated that early antiretroviral therapy (ART) prevented 93% of HIV transmission events in serodiscordant couples. Some linked infections were observed shortly after ART initiation or after virologic failure.

Objective: To evaluate factors associated with time to viral suppression and virologic failure in participants who initiated ART in HPTN 052.

Methods: 1566 participants who had a viral load (VL) > 400 copies/mL at enrollment were included in the analyses. This included 832 in the early ART arm (CD4 350-550 cells/mm3 at ART initiation) and 734 in the delayed ART arm (204 with a CD4 < 250 cells/mm3 at ART initiation; 530 with any CD4 at ART initiation). Viral suppression was defined as two consecutive VLs ≤ 400 copies/mL after ART initiation; virologic failure was defined as two consecutive VLs > 1000 copies/mL > 24 weeks after ART initiation.

Results: Overall, 93% of participants achieved viral suppression by 12 months. The annual incidence of virologic failure was 3.6%. Virologic outcomes were similar in the two study arms. Longer time to viral suppression was associated with younger age, higher VL at ART initiation, and region (Africa vs. Asia). Virologic failure was strongly associated with younger age, lower educational level, and lack of suppression by three months; lower VL and higher CD4 at ART initiation were also associated with virologic failure.

Conclusions: Several clinical and demographic factors were identified that were associated with longer time to viral suppression and virologic failure. Recognition of these factors may help optimize ART for HIV treatment and prevention.

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来源期刊
HIV Clinical Trials
HIV Clinical Trials 医学-传染病学
CiteScore
1.76
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: HIV Clinical Trials is devoted exclusively to presenting information on the latest developments in HIV/AIDS clinical research. This journal enables readers to obtain the most up-to-date, innovative research from around the world.
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