Population-level impact of expanding PrEP coverage by offering long-acting injectable PrEP to MSM in three high-resource settings: a model comparison analysis.


Journal

Journal of the International AIDS Society
ISSN: 1758-2652
Titre abrégé: J Int AIDS Soc
Pays: Switzerland
ID NLM: 101478566

Informations de publication

Date de publication:
07 2023
Historique:
received: 02 11 2022
accepted: 03 05 2023
medline: 14 7 2023
pubmed: 13 7 2023
entrez: 13 7 2023
Statut: ppublish

Résumé

Long-acting injectable cabotegravir (CAB-LA) demonstrated superiority to daily tenofovir disoproxil fumarate/emtricitabine (TDF/FTC) for HIV pre-exposure prophylaxis (PrEP) in the HPTN 083/084 trials. We compared the potential impact of expanding PrEP coverage by offering CAB-LA to men who have sex with men (MSM) in Atlanta (US), Montreal (Canada) and the Netherlands, settings with different HIV epidemics. Three risk-stratified HIV transmission models were independently parameterized and calibrated to local data. In Atlanta, Montreal and the Netherlands, the models, respectively, estimated mean TDF/FTC coverage starting at 29%, 7% and 4% in 2022, and projected HIV incidence per 100 person-years (PY), respectively, decreasing from 2.06 to 1.62, 0.08 to 0.03 and 0.07 to 0.001 by 2042. Expansion of PrEP coverage was simulated by recruiting new CAB-LA users and by switching different proportions of TDF/FTC users to CAB-LA. Population effectiveness and efficiency of PrEP expansions were evaluated over 20 years in comparison to baseline scenarios with TDF/FTC only. Increasing PrEP coverage by 11 percentage points (pp) from 29% to 40% by 2032 was expected to avert a median 36% of new HIV acquisitions in Atlanta. Substantially larger increases (by 33 or 26 pp) in PrEP coverage (to 40% or 30%) were needed to achieve comparable reductions in Montreal and the Netherlands, respectively. A median 17 additional PYs on PrEP were needed to prevent one acquisition in Atlanta with 40% PrEP coverage, compared to 1000+ in Montreal and 4000+ in the Netherlands. Reaching 50% PrEP coverage by 2032 by recruiting CAB-LA users among PrEP-eligible MSM could avert >45% of new HIV acquisitions in all settings. Achieving targeted coverage 5 years earlier increased the impact by 5-10 pp. In the Atlanta model, PrEP expansions achieving 40% and 50% coverage reduced differences in PrEP access between PrEP-indicated White and Black MSM from 23 to 9 pp and 4 pp, respectively. Achieving high PrEP coverage by offering CAB-LA can impact the HIV epidemic substantially if rolled out without delays. These PrEP expansions may be efficient in settings with high HIV incidence (like Atlanta) but not in settings with low HIV incidence (like Montreal and the Netherlands).

Identifiants

pubmed: 37439080
doi: 10.1002/jia2.26109
pmc: PMC10339001
doi:

Substances chimiques

Emtricitabine G70B4ETF4S
Tenofovir 99YXE507IL
cabotegravir HMH0132Z1Q

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e26109

Subventions

Organisme : NIAID NIH HHS
ID : UM1 AI068617
Pays : United States

Informations de copyright

© 2023 The Authors. Journal of the International AIDS Society published by John Wiley & Sons Ltd on behalf of the International AIDS Society.

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Auteurs

Sarah E Stansfield (SE)

Fred Hutchinson Cancer Center, Seattle, Washington, USA.

Jesse Heitner (J)

Massachusetts General Hospital, Boston, Massachusetts, USA.

Kate M Mitchell (KM)

HIV Prevention Trials Network Modelling Centre, Imperial College London, London, UK.
Department of Nursing and Community Health, Glasgow Caledonian University London, London, UK.
MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.

Carla M Doyle (CM)

Department of Epidemiology and Biostatistics, School of Population and Global Health, McGill University, Montréal, Québec, Canada.

Rachael M Milwid (RM)

Department of Epidemiology and Biostatistics, School of Population and Global Health, McGill University, Montréal, Québec, Canada.

Mia Moore (M)

Fred Hutchinson Cancer Center, Seattle, Washington, USA.

Deborah J Donnell (DJ)

Fred Hutchinson Cancer Center, Seattle, Washington, USA.
University of Washington, Seattle, Washington, USA.

Brett Hanscom (B)

Fred Hutchinson Cancer Center, Seattle, Washington, USA.

Yiqing Xia (Y)

Department of Epidemiology and Biostatistics, School of Population and Global Health, McGill University, Montréal, Québec, Canada.

Mathieu Maheu-Giroux (M)

Department of Epidemiology and Biostatistics, School of Population and Global Health, McGill University, Montréal, Québec, Canada.

David van de Vijver (DV)

Viroscience Department, Erasmus Medical Centre, Rotterdam, the Netherlands.

Haoyi Wang (H)

Viroscience Department, Erasmus Medical Centre, Rotterdam, the Netherlands.
Department of Work and Social Psychology, Maastricht University, Maastricht, the Netherlands.

Ruanne Barnabas (R)

Massachusetts General Hospital, Boston, Massachusetts, USA.

Marie-Claude Boily (MC)

MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.

Dobromir T Dimitrov (DT)

Fred Hutchinson Cancer Center, Seattle, Washington, USA.
University of Washington, Seattle, Washington, USA.

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