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.
Adult
Anti-HIV Agents
/ administration & dosage
Canada
Double-Blind Method
France
HIV Infections
/ diagnosis
HIV-1
/ drug effects
Homosexuality, Male
Humans
Incidence
Male
Medication Adherence
Pre-Exposure Prophylaxis
/ methods
Sexual Behavior
Sexual and Gender Minorities
Tenofovir
/ administration & dosage
Journal
The lancet. HIV
ISSN: 2352-3018
Titre abrégé: Lancet HIV
Pays: Netherlands
ID NLM: 101645355
Informations de publication
Date de publication:
02 2020
02 2020
Historique:
received:
14
05
2019
revised:
02
08
2019
accepted:
09
08
2019
pubmed:
1
12
2019
medline:
4
9
2020
entrez:
1
12
2019
Statut:
ppublish
Résumé
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. 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. 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). 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. 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.
Sections du résumé
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.
Identifiants
pubmed: 31784343
pii: S2352-3018(19)30341-8
doi: 10.1016/S2352-3018(19)30341-8
pii:
doi:
Substances chimiques
Anti-HIV Agents
0
Tenofovir
99YXE507IL
Banques de données
ClinicalTrials.gov
['NCT01473472']
Types de publication
Journal Article
Multicenter Study
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e113-e120Investigateurs
Jean-Pierre Aboulker
(JP)
Nathalie Bajos
(N)
Jean-Guy Baril
(JG)
Michel Besnier
(M)
Johan Binesse
(J)
Diane Carette
(D)
Grégoire Cattin
(G)
Antoine Chéret
(A)
Christian Chidiac
(C)
Elias Choucair
(E)
Jean-François Delfraissy
(JF)
Baptiste Demoulin
(B)
Alpha Diallo
(A)
Isabelle Durant-Zaleski
(I)
Véronique Doré
(V)
Nicolas Etien
(N)
Françoise Euphrasie
(F)
Julien Fonsart
(J)
Valérie Foubert
(V)
Séverine Gibowski
(S)
Gabriel Girard
(G)
Brigitte Guillon
(B)
Soizic Le Mestre
(S)
France Lert
(F)
Nicolas Leturque
(N)
Nicolas Lorente
(N)
Anaïs Mennecier
(A)
Michel Morin
(M)
Emmanuelle Netzer
(E)
Joanne Otis
(J)
Armelle Pasquet
(A)
Gilles Peytavin
(G)
Gilles Pialoux
(G)
Marie Préau
(M)
Cécile Rabian
(C)
Willy Rozenbaum
(W)
Luis Sagaon-Teyssier
(L)
Yacine Saïdi
(Y)
Marine Saouzanet
(M)
Marie-Christine Simon
(MC)
Marie Suzan-Monti
(M)
David Thompson
(D)
Julie Timsit
(J)
Benoît Trottier
(B)
Mark Wainberg
(M)
Commentaires et corrections
Type : CommentIn
Informations de copyright
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