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.
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.
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.
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]).
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.
ANRS/Maladies Infectieuses Emergentes, Gilead Sciences, SIDACTION, and Région Ile de France.
For the French translation of the abstract see Supplementary Materials section.
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。
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。
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。
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。
ANRS/Maladies Infectieuses Emergentes、Gilead Sciences、SIDACTION 和法兰西岛大区。