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.
Open accessAbstract
Background 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.Methods 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.Findings 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).Interpretation Doxycycline PEP reduced the occurrence of a first episode of bacterial STI in high-risk men who have sex with men.Funding France Recherche Nord & Sud Sida-HIV Hépatites (ANRS) and Bill & Melinda Gates Foundation.
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STI PEP with doxycycline 200 mg taken after unprotected anal sex among MSM and transgender women reduced incident chlamydia and syphilis by 70% and 73%, respectively, but had no effect on gonorrhea.
“STI PEP in the form of doxycycline 200 mg taken after unprotected anal sex has been studied among MSM and transgender women; results demonstrated reduction in incident chlamydia and syphilis by 70% and 73%, respectively, but no effect on gonorrhea (93).”
From Sexually Transmitted Infections Treatment Guidelines, 2021 (2021) · cites this paper as [93]
Among MSM, doxycycline taken as PEP in a single oral dose ≤24 hours after sex decreased infection with Treponema pallidum and C. trachomatis; however, no substantial effect was observed for infection with N. gonorrhoeae.
“Among MSM, doxycycline taken as PEP in a single oral dose ≤24 hours after sex decreased infection with Treponema pallidum and C. trachomatis; however, no substantial effect was observed for infection with N. gonorrhoeae (93).”
From Sexually Transmitted Infections Treatment Guidelines, 2021 (2021) · cites this paper as [93]
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References 29 · Cited by 449
- Authors
- Molina, J.-M., Charreau, I., Chidiac, C., Pialoux, G., Cua, E., Delaugerre, C., Capitant, C., Rojas-Castro, D., Fonsart, J., Bercot, B., Bébéar, C., Cotte, L., Robineau, O., Raffi, F., Charbonneau, P., Aslan, A., Chas, J., Niedbalski, L., Spire, B., Sagaon-Teyssier, L., Carette, D., Mestre, S. L., Doré, V., Meyer, L., Pintado, C., Loze, B., Gatey, C., Ponscarme, D., Penot, P., Veron, R., Delgado, J., Dalle, E., Parlier, S., Madelaine, I., Danet, M., Mahjoub, N., Mezreb, N., Moudachirou, K., Morel, S., Conort, G., Lorho, F., Meunier, M., Rozenbaum, W., Monfort, C., Foucoin, J., Boissavy, B., Cousseau, S., Huon, S., Danet, M., Djessima, A., Berrebi, V., Adda, A., le Nagat, S., Zarka, L., Berdougo, J., Mzoughi, N., Clement, F., Decouty, A., Chapolard, C., Godinot, M., Adouard-groslafeige, C., Koffi, J., Pansu, A., Becker, A., Pailhes, S., Bonnet, F., Jeanblanc, F., Brochier, C., Teruin, X., Rouby, S., Gilly, L., Etienne, C., Tolonin, F., Breaud, S., Péchenot, V., Bagge, S., Cepitelli, T., Roger, P., Rosenthal, E., Cheret, A., Cornavin, P., Vandamme, S., Lambec, J., Dumon, N., Leclanche, O., Huleux, T., Biekre, R., Melliez, H., Bazus, H., Pasquet, A., Bernaud, C., Besnier, M., Bonnet, B., Hall, N., Cavellec, M., Hue, H., Larmet, L., Colas, M., Choquet, R., Fouéré, S., Netzer, E., Leturque, N., Binesse, J., Foubert, V., Saouzanet, M., Euphrasie, F., Guillon, B., Saïdi, Y., Suzan, M., Cattin, G., Demoulin, B., & Lorente, N.
- Affiliations
- Inserm (FR)
- Hôpital de la Croix-Rousse (FR)
- Hôpital Tenon (FR)
- Laboratoire de Biochimie (FR)
- Université de Bordeaux (FR)
- Centre Hospitalier de Tourcoing (FR)
- Agence Nationale de Recherches sur le Sida et les Hépatites Virales (FR)
- Université Paris-Sud (FR)
- Corresponding author
- Molina, Jean-Michel
- ORCID
- Venue
- The Lancet Infectious Diseases
- Publisher
- Elsevier BV
- Published
- 2018-03
- Volume
- 18
- Issue
- 3
- Pages
- 308-317
- ISSN
- 1473-3099 (ISSN-L)
- OpenAlex
- W2774560050
- Cited by
- 449
- References
- 29
- Citations by year
- 2026: 64 · 2025: 108 · 2024: 103 · 2023: 60 · 2022: 33 · 2021: 22 · 2020: 21 · 2019: 25 · 2018: 11 · 2017: 1
- FWCI
- 12.20
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- The Lancet Infectious Diseases (acceptedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Funders
- Bill and Melinda Gates Foundation
- Institut National de la Santé et de la Recherche Médicale (SC10-US19)
- Agence Nationale de Recherches sur le Sida et les Hépatites Virales
- Centre Hospitalier Universitaire de Bordeaux
- Topics
- Health Sciences › Medicine › Infectious Diseases › HIV/AIDS Research and Interventions
- Life Sciences › Immunology and Microbiology › Microbiology › Reproductive tract infections research
- Health Sciences › Medicine › Epidemiology › HIV, Drug Use, Sexual Risk
- Keywords
- post-exposure prophylaxis, doxycycline, sexually transmitted infections, men who have sex with men, unprotected sex, HIV pre-exposure prophylaxis, tenofovir disoproxil fumarate, emtricitabine, gonorrhea, chlamydia, syphilis, open-label extension
- MeSH terms
- Adolescent, Adult, Anti-Bacterial Agents, Doxycycline, Humans, Male, Middle Aged, Sexually Transmitted Diseases, Homosexuality, Male, Young Adult, Post-Exposure Prophylaxis
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