Effectiveness and safety of bictegravir/emtricitabine/tenofovir alafenamide in HIV late presenters

•Effectiveness of BIC/FTC/TAF was high among HIV late presenters starting ART•In this setting, BIC/FTC/TAF also demonstrated a good safety and tolerability profile•Among people starting ART with AIDS, BIC/FTC/TAF performance was even higher The efficacy of BIC/FTC/TAF in HIV late presenters initiati...

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Veröffentlicht in:International journal of antimicrobial agents 2024-01, Vol.63 (1), p.107016-107016, Article 107016
Hauptverfasser: Corona, Diana, Pérez-Valero, Ignacio, Camacho, Angela, Liarte, Ángela Gutiérrez, Montero-Alonso, Marta, Alemán, María Remedios, Ruiz-Seco, Pilar, González, Alexandre Pérez, Riera, Melchor, Jarrin, Inmaculada, Rivero-Juárez, Antonio, Rivero, Antonio
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container_end_page 107016
container_issue 1
container_start_page 107016
container_title International journal of antimicrobial agents
container_volume 63
creator Corona, Diana
Pérez-Valero, Ignacio
Camacho, Angela
Liarte, Ángela Gutiérrez
Montero-Alonso, Marta
Alemán, María Remedios
Ruiz-Seco, Pilar
González, Alexandre Pérez
Riera, Melchor
Jarrin, Inmaculada
Rivero-Juárez, Antonio
Rivero, Antonio
description •Effectiveness of BIC/FTC/TAF was high among HIV late presenters starting ART•In this setting, BIC/FTC/TAF also demonstrated a good safety and tolerability profile•Among people starting ART with AIDS, BIC/FTC/TAF performance was even higher The efficacy of BIC/FTC/TAF in HIV late presenters initiating ART has not been sufficiently evaluated. The aim of this study was to assess the effectiveness and tolerability of BIC/FTC/TAF compared to other first-line antiretroviral regimens in treatment-naïve adult individuals from the CoRIS Cohort starting ART with CD4 counts
doi_str_mv 10.1016/j.ijantimicag.2023.107016
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The aim of this study was to assess the effectiveness and tolerability of BIC/FTC/TAF compared to other first-line antiretroviral regimens in treatment-naïve adult individuals from the CoRIS Cohort starting ART with CD4 counts &lt;200 cells/mm3 and/or AIDS-defining conditions between Jan 1, 2019 and Nov 30, 2020. Logistic regression models were used to estimate odds ratios (ORs) of association between initial regimen and achievement of viral suppression (VS) (primary objective), defined as HIV RNA &lt;50 cop/ml, and immunological recovery (IR) (secondary objective), defined as CD4 count &gt;200 cells/mm3, at weeks 24 and 48 after initiation of ART. We evaluated 314 individuals (84.7% men, median age 40 years). Of them, 158 initiated with BIC/FTC/TAF. At inclusion, 117 had an AIDS-defining condition. In multivariable analyses, individuals with AIDS-defining conditions initiating ART with BIC/FTC/TAF achieved higher rates of VS at 24 weeks than other regimens (aOR: 0.2; 95%CI: 0.06 – 0.64) and, at 48 weeks than DTG/ABC/3TC (aOR: 0.06; 95%CI: 0.01 – 0.76) and DTG + TDF/3TC (aOR: 0.2; 95% CI: 0.47 – 0.9). No other differences in VS or IR were observed. At 24 and 48 weeks after ART initiation, treatment discontinuations were lower with BIC/FTC/TAF than with other regimens (3.2% and 7.6% vs. 24.4% and 37.8%, respectively; p&lt;0.005). Our results suggest that BIC/FTC/TAF could be a preferred regimen as initial therapy in HIV late presenters due to its high effectiveness and good tolerability.</description><identifier>ISSN: 0924-8579</identifier><identifier>EISSN: 1872-7913</identifier><identifier>DOI: 10.1016/j.ijantimicag.2023.107016</identifier><identifier>PMID: 37890734</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Acquired Immunodeficiency Syndrome - drug therapy ; Adult ; adults ; Alanine ; Amides ; Anti-HIV Agents - adverse effects ; antiretroviral agents ; Coris ; Drug Combinations ; Emtricitabine - adverse effects ; Female ; Heterocyclic Compounds, 3-Ring ; HIV Infections - drug therapy ; Humans ; Male ; Piperazines ; Pyridones ; regression analysis ; RNA ; Tenofovir - analogs &amp; derivatives ; therapeutics</subject><ispartof>International journal of antimicrobial agents, 2024-01, Vol.63 (1), p.107016-107016, Article 107016</ispartof><rights>2023</rights><rights>Copyright © 2023 The Authors. Published by Elsevier Ltd.. 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The aim of this study was to assess the effectiveness and tolerability of BIC/FTC/TAF compared to other first-line antiretroviral regimens in treatment-naïve adult individuals from the CoRIS Cohort starting ART with CD4 counts &lt;200 cells/mm3 and/or AIDS-defining conditions between Jan 1, 2019 and Nov 30, 2020. Logistic regression models were used to estimate odds ratios (ORs) of association between initial regimen and achievement of viral suppression (VS) (primary objective), defined as HIV RNA &lt;50 cop/ml, and immunological recovery (IR) (secondary objective), defined as CD4 count &gt;200 cells/mm3, at weeks 24 and 48 after initiation of ART. We evaluated 314 individuals (84.7% men, median age 40 years). Of them, 158 initiated with BIC/FTC/TAF. At inclusion, 117 had an AIDS-defining condition. In multivariable analyses, individuals with AIDS-defining conditions initiating ART with BIC/FTC/TAF achieved higher rates of VS at 24 weeks than other regimens (aOR: 0.2; 95%CI: 0.06 – 0.64) and, at 48 weeks than DTG/ABC/3TC (aOR: 0.06; 95%CI: 0.01 – 0.76) and DTG + TDF/3TC (aOR: 0.2; 95% CI: 0.47 – 0.9). No other differences in VS or IR were observed. At 24 and 48 weeks after ART initiation, treatment discontinuations were lower with BIC/FTC/TAF than with other regimens (3.2% and 7.6% vs. 24.4% and 37.8%, respectively; p&lt;0.005). 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The aim of this study was to assess the effectiveness and tolerability of BIC/FTC/TAF compared to other first-line antiretroviral regimens in treatment-naïve adult individuals from the CoRIS Cohort starting ART with CD4 counts &lt;200 cells/mm3 and/or AIDS-defining conditions between Jan 1, 2019 and Nov 30, 2020. Logistic regression models were used to estimate odds ratios (ORs) of association between initial regimen and achievement of viral suppression (VS) (primary objective), defined as HIV RNA &lt;50 cop/ml, and immunological recovery (IR) (secondary objective), defined as CD4 count &gt;200 cells/mm3, at weeks 24 and 48 after initiation of ART. We evaluated 314 individuals (84.7% men, median age 40 years). Of them, 158 initiated with BIC/FTC/TAF. At inclusion, 117 had an AIDS-defining condition. In multivariable analyses, individuals with AIDS-defining conditions initiating ART with BIC/FTC/TAF achieved higher rates of VS at 24 weeks than other regimens (aOR: 0.2; 95%CI: 0.06 – 0.64) and, at 48 weeks than DTG/ABC/3TC (aOR: 0.06; 95%CI: 0.01 – 0.76) and DTG + TDF/3TC (aOR: 0.2; 95% CI: 0.47 – 0.9). No other differences in VS or IR were observed. At 24 and 48 weeks after ART initiation, treatment discontinuations were lower with BIC/FTC/TAF than with other regimens (3.2% and 7.6% vs. 24.4% and 37.8%, respectively; p&lt;0.005). 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subjects Acquired Immunodeficiency Syndrome - drug therapy
Adult
adults
Alanine
Amides
Anti-HIV Agents - adverse effects
antiretroviral agents
Coris
Drug Combinations
Emtricitabine - adverse effects
Female
Heterocyclic Compounds, 3-Ring
HIV Infections - drug therapy
Humans
Male
Piperazines
Pyridones
regression analysis
RNA
Tenofovir - analogs & derivatives
therapeutics
title Effectiveness and safety of bictegravir/emtricitabine/tenofovir alafenamide in HIV late presenters
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