Post-exposure prophylaxis with doxycycline ...
Document type :
Article dans une revue scientifique: Article original
PMID :
Permalink :
Title :
Post-exposure prophylaxis with doxycycline to prevent sexually transmitted infections in men who have sex with men: an open-label randomised substudy of the anrs ipergay trial
Author(s) :
Molina, Jean-Michel [Auteur]
Charreau, Isabelle [Auteur]
Chidiac, Christian [Auteur]
Pialoux, Gilles [Auteur]
Cua, Eric [Auteur]
Delaugerre, Constance [Auteur]
Capitant, Catherine [Auteur]
Rojas-Castro, Daniela [Auteur]
Fonsart, Julien [Auteur]
Bercot, Beatrice [Auteur]
Bebear, Cecile [Auteur]
Cotte, Laurent [Auteur]
Robineau, Olivier [Auteur]
Centre Hospitalier Gustave Dron [Tourcoing]
Raffi, François [Auteur]
Charbonneau, Pierre [Auteur]
Aslan, Alexandre [Auteur]
Chas, Julie [Auteur]
Niedbalski, Laurence [Auteur]
Spire, Bruno [Auteur]
Sagaon-Teyssier, Luis [Auteur]
Carette, Diane [Auteur]
Le Mestre, Soizic [Auteur]
Dore, Veronique [Auteur]
Meyer, Laurence [Auteur]
Charreau, Isabelle [Auteur]
Chidiac, Christian [Auteur]
Pialoux, Gilles [Auteur]
Cua, Eric [Auteur]
Delaugerre, Constance [Auteur]
Capitant, Catherine [Auteur]
Rojas-Castro, Daniela [Auteur]
Fonsart, Julien [Auteur]
Bercot, Beatrice [Auteur]
Bebear, Cecile [Auteur]
Cotte, Laurent [Auteur]
Robineau, Olivier [Auteur]
Centre Hospitalier Gustave Dron [Tourcoing]
Raffi, François [Auteur]
Charbonneau, Pierre [Auteur]
Aslan, Alexandre [Auteur]
Chas, Julie [Auteur]
Niedbalski, Laurence [Auteur]
Spire, Bruno [Auteur]
Sagaon-Teyssier, Luis [Auteur]
Carette, Diane [Auteur]
Le Mestre, Soizic [Auteur]
Dore, Veronique [Auteur]
Meyer, Laurence [Auteur]
Journal title :
The Lancet Infectious Diseases
Abbreviated title :
Lancet Infect. Dis.
Volume number :
18
Pages :
308-317
Publication date :
2018-03-01
ISSN :
1473-3099
HAL domain(s) :
Sciences du Vivant [q-bio]
English abstract : [en]
Increased rates of sexually transmitted infections (STIs) have been reported among men who have sex with men. We aimed to assess whether post-exposure prophylaxis (PEP) with doxycycline could reduce the incidence of ...
Show more >Increased rates of sexually transmitted infections (STIs) have been reported among men who have sex with men. We aimed to assess whether post-exposure prophylaxis (PEP) with doxycycline could reduce the incidence of STIs. All participants attending their scheduled visit in the open-label extension of the ANRS IPERGAY trial in France (men aged 18 years or older having condomless sex with men and using pre-exposure prophylaxis for HIV with tenofovir disoproxil fumarate plus emtricitabine) were eligible for inclusion in this open-label randomised study. Participants were randomly assigned (1:1) at a central site to take a single oral dose of 200 mg doxycycline PEP within 24 h after sex or no prophylaxis. The primary endpoint was the occurrence of a first STI (gonorrhoea, chlamydia, or syphilis) during the 10-month follow-up. The cumulative probability of occurrence of the primary endpoint was estimated in each group with the Kaplan-Meier method and compared with the log-rank test. The primary efficacy analysis was done on the intention-to-treat population, comprising all randomised participants. All participants received risk-reduction counselling and condoms, and were tested regularly for HIV. This trial is registered with ClinicalTrials.gov number, NCT01473472. Between July 20, 2015, and Jan 21, 2016, we randomly assigned 232 participants (n=116 in the doxycycline PEP group and n=116 in the no-PEP group) who were followed up for a median of 8·7 months (IQR 7·8-9·7). Participants in the PEP group used a median of 680 mg doxycycline per month (IQR 280-1450). 73 participants presented with a new STI during follow-up, 28 in the PEP group (9-month probability 22%, 95% CI 15-32) and 45 in the no-PEP group (42%, 33-53; log-rank test p=0·007). The occurrence of a first STI in participants taking PEP was lower than in those not taking PEP (hazard ratio [HR] 0·53; 95% CI 0·33-0·85; p=0·008). Similar results were observed for the occurrence of a first episode of chlamydia (HR 0·30; 95% CI 0·13-0·70; p=0·006) and of syphilis (0·27; 0·07-0·98; p=0·047); for a first episode of gonorrhoea the results did not differ significantly (HR 0·83; 0·47-1·47; p=0·52). No HIV seroconversion was observed, and 72 (71%) of all 102 STIs were asymptomatic. Rates of serious adverse events were similar in the two study groups. Gastrointestinal adverse events were reported in 62 (53%) participants in the PEP group and 47 (41%) in the no-PEP group (p=0·05). Doxycycline PEP reduced the occurrence of a first episode of bacterial STI in high-risk men who have sex with men. France Recherche Nord & Sud Sida-HIV Hépatites (ANRS) and Bill & Melinda Gates Foundation.Show less >
Show more >Increased rates of sexually transmitted infections (STIs) have been reported among men who have sex with men. We aimed to assess whether post-exposure prophylaxis (PEP) with doxycycline could reduce the incidence of STIs. All participants attending their scheduled visit in the open-label extension of the ANRS IPERGAY trial in France (men aged 18 years or older having condomless sex with men and using pre-exposure prophylaxis for HIV with tenofovir disoproxil fumarate plus emtricitabine) were eligible for inclusion in this open-label randomised study. Participants were randomly assigned (1:1) at a central site to take a single oral dose of 200 mg doxycycline PEP within 24 h after sex or no prophylaxis. The primary endpoint was the occurrence of a first STI (gonorrhoea, chlamydia, or syphilis) during the 10-month follow-up. The cumulative probability of occurrence of the primary endpoint was estimated in each group with the Kaplan-Meier method and compared with the log-rank test. The primary efficacy analysis was done on the intention-to-treat population, comprising all randomised participants. All participants received risk-reduction counselling and condoms, and were tested regularly for HIV. This trial is registered with ClinicalTrials.gov number, NCT01473472. Between July 20, 2015, and Jan 21, 2016, we randomly assigned 232 participants (n=116 in the doxycycline PEP group and n=116 in the no-PEP group) who were followed up for a median of 8·7 months (IQR 7·8-9·7). Participants in the PEP group used a median of 680 mg doxycycline per month (IQR 280-1450). 73 participants presented with a new STI during follow-up, 28 in the PEP group (9-month probability 22%, 95% CI 15-32) and 45 in the no-PEP group (42%, 33-53; log-rank test p=0·007). The occurrence of a first STI in participants taking PEP was lower than in those not taking PEP (hazard ratio [HR] 0·53; 95% CI 0·33-0·85; p=0·008). Similar results were observed for the occurrence of a first episode of chlamydia (HR 0·30; 95% CI 0·13-0·70; p=0·006) and of syphilis (0·27; 0·07-0·98; p=0·047); for a first episode of gonorrhoea the results did not differ significantly (HR 0·83; 0·47-1·47; p=0·52). No HIV seroconversion was observed, and 72 (71%) of all 102 STIs were asymptomatic. Rates of serious adverse events were similar in the two study groups. Gastrointestinal adverse events were reported in 62 (53%) participants in the PEP group and 47 (41%) in the no-PEP group (p=0·05). Doxycycline PEP reduced the occurrence of a first episode of bacterial STI in high-risk men who have sex with men. France Recherche Nord & Sud Sida-HIV Hépatites (ANRS) and Bill & Melinda Gates Foundation.Show less >
Language :
Anglais
Audience :
Internationale
Popular science :
Non
Administrative institution(s) :
CHU Lille
Université de Lille
Université de Lille
Submission date :
2019-12-09T16:49:50Z
2024-04-03T10:12:12Z
2024-04-03T10:12:12Z