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按需服用富马酸替诺福韦二吡呋酯和恩曲他滨的男男性行为者中,性行为频率较低者的事前预防:ANRS IPERGAY 试验的事后分析。

On-demand pre-exposure prophylaxis with tenofovir disoproxil fumarate plus emtricitabine among men who have sex with men with less frequent sexual intercourse: a post-hoc analysis of the ANRS IPERGAY trial.

机构信息

Institut national de la santé et de la recherche médicale (INSERM) SC10 US19, Villejuif, France.

Centre Hospitalier de l'Université de Montréal, Montreal, QC, Canada.

出版信息

Lancet HIV. 2020 Feb;7(2):e113-e120. doi: 10.1016/S2352-3018(19)30341-8. Epub 2019 Nov 26.

Abstract

BACKGROUND

ANRS IPERGAY found that on-demand pre-exposure prophylaxis (PrEP) with oral tenofovir disoproxil fumarate plus emtricitabine was associated with an 86% relative reduction of HIV-1 incidence compared with placebo among men who have sex with men at high risk of HIV. We aimed to investigate whether on-demand PrEP was similarly effective among individuals with lower exposure to HIV risk.

METHODS

Participants in the ANRS IPERGAY trial were randomly assigned to receive PrEP (fixed-dose combination of 300 mg tenofovir disoproxil fumarate and 200 mg emtricitabine per pill) or placebo. The primary endpoint was the diagnosis of HIV-1 infection. Pill uptake was assessed by counting returned pills at each follow-up and by estimating tenofovir concentration from frozen plasma samples. Participants were interviewed at each visit to assess the pattern of PrEP use. All participants enrolled in the modified intention-to-treat population of the double-blind phase of the ANRS IPERGAY trial were eligible for this post-hoc analysis. We calculated the total follow-up time for periods of less frequent sexual intercourse with high PrEP adherence (15 pills or fewer per month taken systematically or often during sexual intercourse). To estimate the time of HIV acquisition, fourth-generation HIV-1/2 ELISA assays, plasma HIV-1 RNA assays, and western blot analyses were done with use of frozen samples, and the stage of HIV infection was defined according to Fiebig staging. HIV incidence was compared between the two treatment groups among individuals who had less frequent sexual intercourse with high PrEP adherence. The ANRS IPERGAY trial is registered with ClinicalTrials.gov, NCT01473472.

FINDINGS

400 participants who were randomly assigned to receive PrEP (n=199) or placebo (n=201) between Feb 22, 2012, and Oct 17, 2014, were included in this analysis. 270 participants had at least one period of less frequent sexual intercourse with high PrEP adherence during the study, representing 134 person-years of follow-up and 31% of the total study follow-up. During these periods, participants in both groups reported a median of 5·0 (IQR 2·0-10·0) episodes of sexual intercourse per month and used a median of 9·5 (6·0-13·0) pills per month. Six HIV-1 infections were diagnosed in the placebo group (HIV incidence of 9·2 per 100 person-years; 95% CI 3·4-20·1) and none were diagnosed in the tenofovir disoproxil fumarate plus emtricitabine arm (HIV incidence of 0 per 100 person-years; 0-5·4; p=0·013), with a relative reduction of HIV incidence of 100% (95% CI 39-100).

INTERPRETATION

A choice between daily or on-demand PrEP regimens could be offered to men who have sex with men who have less frequent sexual intercourse.

FUNDING

ANRS (France Recherche Nord and Sud Sida-HIV Hépatites), the Canadian HIV Trials Network, Fonds Pierre Bergé (Sidaction), Gilead Sciences, and the Bill & Melinda Gates Foundation.

摘要

背景

ANRS IPERGAY 发现,与安慰剂相比,对于有较高 HIV 感染风险的男男性行为者,按需服用口服替诺福韦酯富马酸二吡呋酯和恩曲他滨的暴露前预防(PrEP)可使 HIV-1 发病率相对降低 86%。我们旨在研究在 HIV 风险暴露较低的个体中,按需 PrEP 是否同样有效。

方法

ANRS IPERGAY 试验中的参与者被随机分配接受 PrEP(每片 300mg 替诺福韦酯富马酸二吡呋酯和 200mg 恩曲他滨的固定剂量组合)或安慰剂。主要终点是 HIV-1 感染的诊断。通过每次随访时清点返还的药丸和通过从冷冻血浆样本中估计替诺福韦浓度来评估药丸摄取情况。每次就诊时,参与者都会接受采访,以评估 PrEP 使用模式。所有参加 ANRS IPERGAY 试验双盲阶段改良意向治疗人群的参与者均有资格进行此项事后分析。我们计算了在高 PrEP 依从性下(每月系统服用或经常在性行为期间服用 15 片或更少)较少性行为的时间段内的总随访时间。为了估计 HIV 获得的时间,使用冷冻样本进行了第四代 HIV-1/2 ELISA 检测、血浆 HIV-1 RNA 检测和 Western blot 分析,根据 Fiebig 分期定义了 HIV 感染的阶段。在高 PrEP 依从性且较少性行为的个体中,比较了两组之间的 HIV 发病率。ANRS IPERGAY 试验在 ClinicalTrials.gov 注册,NCT01473472。

结果

2012 年 2 月 22 日至 2014 年 10 月 17 日期间,随机分配接受 PrEP(n=199)或安慰剂(n=201)的 400 名参与者被纳入本分析。270 名参与者在研究期间至少有一次低频率性行为和高 PrEP 依从性,代表了 134 人年的随访和总研究随访的 31%。在这些期间,两组参与者报告的每月平均性行为次数中位数为 5.0(IQR 2.0-10.0),每月平均使用药丸中位数为 9.5(6.0-13.0)。安慰剂组诊断出 6 例 HIV-1 感染(HIV 发病率为 9.2/100 人年;95%CI 3.4-20.1),而替诺福韦酯富马酸二吡呋酯加恩曲他滨组未诊断出 HIV-1 感染(HIV 发病率为 0/100 人年;0-5.4;p=0.013),HIV 发病率相对降低 100%(95%CI 39-100)。

结论

对于性行为频率较低的男男性行为者,可以选择每日或按需 PrEP 方案。

资助

ANRS(法国北部和南部艾滋病-艾滋病毒肝炎)、加拿大艾滋病毒试验网络、皮埃尔·伯格基金会(Sidaction)、吉利德科学公司和比尔和梅琳达·盖茨基金会。

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