Université de Paris Cité, Paris, France; Département de Maladies Infectieuses et Laboratoires de Virologie et de Pharmacologie, Hôpitaux Saint-Louis, Lariboisière, Assistance Publique Hôpitaux de Paris, Paris, France; INSERM UMR 944, Paris, France.
Université de Paris Cité, Paris, France; Département de Maladies Infectieuses et Laboratoires de Virologie et de Pharmacologie, Hôpitaux Saint-Louis, Lariboisière, Assistance Publique Hôpitaux de Paris, Paris, France; Department of Infectious Diseases, Hopital Bichat Claude Bernard and INSERM UMR 1137 IAME, Paris, France.
Lancet HIV. 2022 Aug;9(8):e554-e562. doi: 10.1016/S2352-3018(22)00133-3. Epub 2022 Jun 27.
BACKGROUND: There are few data available regarding the use of on-demand pre-exposure prophylaxis (PrEP) for HIV prevention. We aimed to assess PrEP effectiveness, adherence, and safety in adults using daily or on-demand PrEP. METHODS: We conducted a prospective observational cohort study (ANRS PREVENIR) at 26 sites in the Paris region, France. We enrolled HIV-negative adults (aged ≥18 years) at high risk of HIV infection who were starting or continuing PrEP. PrEP was prescribed as a fixed-dose combination of tenofovir disoproxil and emtricitabine (245 mg and 200 mg, respectively, per pill). PrEP could be prescribed as a daily regimen with one pill per day or, in men who have sex with men (MSM) or in transgender women who have sex with men, as an on-demand regimen following the IPERGAY dosing recommendation. At enrolment and every 3 months thereafter, participants were tested for HIV and provided information regarding the PrEP dosing regimen used. Adherence to PrEP was assessed by self-report and by tenofovir diphosphate concentrations in dried blood spots. The primary outcome of HIV-1 incidence was assessed using Poisson regression among participants who started PrEP. This study is registered with ClinicalTrials.gov, NCT03113123, and EudraCT, 2016A0157744. FINDINGS: Between May 3, 2017, and May 2, 2019, 3082 people were assessed for eligibility and 3065 participants were enrolled. 3056 (99·7%) of 3065 participants reported using PrEP and were included in the analyses. The median age was 36 years (IQR 29-43), 1344 (44·0%) of 3056 participants were PrEP-naive, and 3016 (98·7%) were MSM. At enrolment, 1540 (50·5%) of 3049 participants opted for daily PrEP dosing and 1509 (49·5%) opted for on-demand PrEP dosing; these proportions remained stable during follow-up. Median follow-up was 22·1 months (IQR 15·9-29·7) and incidence of study discontinuation was 17·6 participants (95% CI 16·5-18·7) per 100 person-years. At the data cutoff on Sept 30, 2020, there had been six HIV-1 seroconversions (three participants using daily PrEP and three using on-demand PrEP; all were MSM) over 5623 person-years. Overall HIV-1 incidence was 1·1 cases (95% CI 0·4-2·3) per 1000 person-years, and did not differ between participants using daily PrEP and those using on-demand PrEP (incidence rate ratio 1·00, 95% CI 0·13-7·49; p=0·99). Four participants (two using daily PrEP and two using on-demand PrEP) discontinued PrEP due to treatment-related adverse events (nausea [n=2], vomiting and diarrhoea [n=1], and lumbar pain [n=1]). INTERPRETATION: In this study, which enrolled mainly MSM, HIV-1 incidence on PrEP was low and did not differ between participants using daily PrEP and those using on-demand PrEP. On-demand PrEP therefore represents a valid alternative to daily PrEP for MSM, providing greater choice in HIV prevention. FUNDING: ANRS/Maladies Infectieuses Emergentes, Gilead Sciences, SIDACTION, and Région Ile de France. TRANSLATION: For the French translation of the abstract see Supplementary Materials section.
背景:目前关于按需暴露前预防(PrEP)用于 HIV 预防的数据有限。我们旨在评估使用每日或按需 PrEP 的成年人中 PrEP 的有效性、依从性和安全性。
方法:我们在法国巴黎地区的 26 个地点进行了一项前瞻性观察性队列研究(ANRS PREVENIR)。我们招募了 HIV 阴性、有感染 HIV 高风险的成年人(年龄≥18 岁),他们正在开始或继续使用 PrEP。PrEP 被开为替诺福韦地索普西和恩曲他滨的固定剂量组合(每片分别为 245mg 和 200mg)。PrEP 可以规定为每日方案,每天服用一片,或者对于男男性行为者(MSM)或与男性发生性行为的变性女性,可以根据 IPERGAY 剂量建议按需服用。在入组时和此后每 3 个月,参与者接受 HIV 检测,并提供他们使用的 PrEP 剂量方案信息。通过自我报告和干血斑中替诺福韦二磷酸浓度评估 PrEP 的依从性。通过泊松回归评估 HIV-1 发病率作为主要结局,参与者在开始 PrEP 时进行评估。这项研究在 ClinicalTrials.gov 注册,NCT03113123 和 EudraCT,2016A0157744。
结果:2017 年 5 月 3 日至 2019 年 5 月 2 日,评估了 3082 人是否符合入选条件,有 3065 人入组。3056 名(99.7%)报告使用 PrEP 的 3065 名参与者被纳入分析。中位年龄为 36 岁(IQR 29-43),3056 名参与者中 1344 名(44.0%)为 PrEP 初治者,3016 名(98.7%)为 MSM。入组时,1540 名(50.5%)的 3049 名参与者选择每日 PrEP 剂量,1509 名(49.5%)选择按需 PrEP 剂量;在随访期间,这些比例保持稳定。中位随访时间为 22.1 个月(IQR 15.9-29.7),研究中止率为 17.6 名(95%CI 16.5-18.7)/100 人年。截至 2020 年 9 月 30 日数据截止日期,5623 人年中发生了 6 例 HIV-1 血清转化(3 名使用每日 PrEP 的参与者和 3 名使用按需 PrEP 的参与者;均为 MSM)。总体 HIV-1 发病率为 1.1 例(95%CI 0.4-2.3)/1000 人年,每日 PrEP 组和按需 PrEP 组之间无差异(发病率比 1.00,95%CI 0.13-7.49;p=0.99)。4 名参与者(每日 PrEP 组 2 名,按需 PrEP 组 2 名)因治疗相关不良事件(恶心[2 名]、呕吐和腹泻[1 名]和腰痛[1 名])停用 PrEP。
解释:在这项主要招募 MSM 的研究中,PrEP 相关的 HIV-1 发病率较低,每日 PrEP 组和按需 PrEP 组之间无差异。因此,按需 PrEP 是 MSM 预防 HIV 的有效替代方案,为 HIV 预防提供了更多选择。
资金:ANRS/Maladies Infectieuses Emergentes、Gilead Sciences、SIDACTION 和法兰西岛大区。
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