Prevalence and Outcomes for Heavily Treatment-Experienced Individuals Living With Human Immunodeficiency Virus in a European Cohort.


Journal

Journal of acquired immune deficiency syndromes (1999)
ISSN: 1944-7884
Titre abrégé: J Acquir Immune Defic Syndr
Pays: United States
ID NLM: 100892005

Informations de publication

Date de publication:
01 06 2021
Historique:
received: 15 07 2020
accepted: 01 12 2020
pubmed: 16 2 2021
medline: 7 10 2021
entrez: 15 2 2021
Statut: ppublish

Résumé

Although antiretroviral treatments have improved survival of persons living with HIV, their long-term use may limit available drug options. We estimated the prevalence of heavily treatment-experienced (HTE) status and the potential clinical consequences of becoming HTE. EuroSIDA, a European multicenter prospective cohort study. A composite definition for HTE was developed, based on estimates of antiretroviral resistance and prior exposure to specific antiretroviral regimens. Risks of progressing to clinical outcomes were assessed by Poisson regression, comparing every HTE individual with 3 randomly selected controls who never became HTE. Of 15,570 individuals under follow-up in 2010-2016, 1617 (10.4%, 95% CI: 9.9% to 10.9%) were classified as HTE. 1093 individuals became HTE during prospective follow-up (HTE incidence rate 1.76, CI: 1.66 to 1.87 per 100 person-years of follow-up). The number of HTE individuals was highest in West/Central Europe (636/4019 persons, 15.7%) and lowest in East Europe (26/2279 persons, 1.1%). Although most HTE individuals maintained controlled viral loads (<400 copies/mL), many had low CD4 counts (≤350 cells/µL). After controlling for age, immunological parameters and pre-existing comorbidities, HTE status was not associated with the risk of new AIDS (adjusted incidence rate ratio, aIRR 1.44, CI: 0.86 to 2.40, P = 0.16) or non-AIDS clinical events (aIRR 0.96, CI: 0.74 to 1.25, P = 0.77). HTE prevalence increased with time. After adjusting for key confounding factors, there was no evidence for an increased risk of new AIDS or non-AIDS clinical events in HTE. Additional therapeutic options and effective management of comorbidities remain important to reduce clinical complications in HTE individuals.

Sections du résumé

BACKGROUND
Although antiretroviral treatments have improved survival of persons living with HIV, their long-term use may limit available drug options. We estimated the prevalence of heavily treatment-experienced (HTE) status and the potential clinical consequences of becoming HTE.
SETTING
EuroSIDA, a European multicenter prospective cohort study.
METHODS
A composite definition for HTE was developed, based on estimates of antiretroviral resistance and prior exposure to specific antiretroviral regimens. Risks of progressing to clinical outcomes were assessed by Poisson regression, comparing every HTE individual with 3 randomly selected controls who never became HTE.
RESULTS
Of 15,570 individuals under follow-up in 2010-2016, 1617 (10.4%, 95% CI: 9.9% to 10.9%) were classified as HTE. 1093 individuals became HTE during prospective follow-up (HTE incidence rate 1.76, CI: 1.66 to 1.87 per 100 person-years of follow-up). The number of HTE individuals was highest in West/Central Europe (636/4019 persons, 15.7%) and lowest in East Europe (26/2279 persons, 1.1%). Although most HTE individuals maintained controlled viral loads (<400 copies/mL), many had low CD4 counts (≤350 cells/µL). After controlling for age, immunological parameters and pre-existing comorbidities, HTE status was not associated with the risk of new AIDS (adjusted incidence rate ratio, aIRR 1.44, CI: 0.86 to 2.40, P = 0.16) or non-AIDS clinical events (aIRR 0.96, CI: 0.74 to 1.25, P = 0.77).
CONCLUSIONS
HTE prevalence increased with time. After adjusting for key confounding factors, there was no evidence for an increased risk of new AIDS or non-AIDS clinical events in HTE. Additional therapeutic options and effective management of comorbidities remain important to reduce clinical complications in HTE individuals.

Identifiants

pubmed: 33587506
doi: 10.1097/QAI.0000000000002635
pii: 00126334-202106010-00012
doi:

Substances chimiques

Anti-HIV Agents 0

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

806-817

Informations de copyright

Copyright © 2021 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

A.P.-M. reports personal fees from Gilead Sciences outside the submitted work; A.H.B was supported by Lundbeckfonden during the conduct of this study; J.B. reports personal fees from MSD, ViiV Healthcare, and Gilead Sciences outside the submitted work; and A.C. is employed by ViiV Healthcare. The remaining authors have no conflicts of interest to disclose.

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Auteurs

Annegret Pelchen-Matthews (A)

Centre for Clinical Research, Epidemiology, Modelling and Evaluation (CREME), Institute for Global Health, University College London, London, United Kingdom.

Álvaro H Borges (ÁH)

Department of Infectious Diseases Immunology, Statens Serum Institut, Copenhagen, Denmark.

Joanne Reekie (J)

Department of Infectious Diseases, Centre for Health and Infectious Disease Research, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Line D Rasmussen (LD)

Department of Infectious Diseases, Odense University Hospital, Odense, Denmark.

Lothar Wiese (L)

Sjællands Universitetshospital, Roskilde, Denmark.

Jonathan Weber (J)

St. Mary's Hospital, London, United Kingdom.

Christian Pradier (C)

CHU Nice Hopital de l' Archet 1, Nice, France.

Olaf Degen (O)

University Clinic Hamburg Eppendorf, Hamburg, Germany.

Roger Paredes (R)

Hospital Universitari Germans Trias i Pujol, Badalona, Spain.

Luba Tau (L)

Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.

Leo Flamholc (L)

Skåne University Hospital, Malmö, Sweden.

Magnus Gottfredsson (M)

Faculty of Medicine, University of Iceland, Reykjavik, Iceland.

Justyna Kowalska (J)

Medical University of Warsaw, Warsaw, Poland.

Elzbieta Jablonowska (E)

Clinic of Infectious Diseases and Hepatology, Medical University of Lodz, Lodz, Poland.

Iwona Mozer-Lisewska (I)

Poznan University of Medical Sciences, Poznan, Poland.

Roxana Radoi (R)

Victor Babes Clinical Hospital for Infectious and Tropical Diseases, Bucharest, Romania.

Marta Vasylyev (M)

HIV Unit, Lviv Regional Public Health Center, Lviv, Ukraine.

Anastasiia Kuznetsova (A)

Kharkov State Medical University, Kharkov, Ukraine.

Josip Begovac (J)

University Hospital for Infectious Diseases Dr. Fran Mihaljević, Zagreb, Croatia.

Veronica Svedhem (V)

Infectious Diseases Department, Karolinska University Hospital, Infectious Diseases Department, Stockholm, Sweden ; and.

Andrew Clark (A)

ViiV Healthcare, London, United Kingdom .

Alessandro Cozzi-Lepri (A)

Centre for Clinical Research, Epidemiology, Modelling and Evaluation (CREME), Institute for Global Health, University College London, London, United Kingdom.

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