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

Objectives: The efficacy of BIC/FTC/TAF in HIV late presenters initiating antiretroviral therapy (ART) has not been sufficiently evaluated. Methods: 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...

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Autores: Corona, Diana, Pérez-Valero, Ignacio, Camacho, Angela, Gutiérrez Liarte, Ángela, Montero-Alonso, Marta, Alemán, María Remedios, Ruiz-Seco, Pilar, Pérez González, Alexandre, Riera, Melchor, Jarrin Vera, Inmaculada, Rivero-Juarez, Antonio, Rivero, Antonio
Tipo de recurso: artículo
Fecha de publicación:2024
País:España
Institución:Instituto de Salud Carlos III (ISCIII)
Repositorio:Repisalud
Idioma:inglés
OAI Identifier:oai:repisalud.isciii.es:20.500.12105/18995
Acceso en línea:http://hdl.handle.net/20.500.12105/18995
Access Level:acceso abierto
Palabra clave:Anti-HIV Agents
Acquired Immunodeficiency Syndrome
HIV Infections
Piperazines
Pyridones
Alanine
Amides
Heterocyclic Compounds, 3-Ring
Adult
Male
Humans
Female
Drug Combinations
Emtricitabine
Tenofovir
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spelling Effectiveness and safety of bictegravir/emtricitabine/tenofovir alafenamide in HIV late presentersCorona, DianaPérez-Valero, IgnacioCamacho, AngelaGutiérrez Liarte, ÁngelaMontero-Alonso, MartaAlemán, María RemediosRuiz-Seco, PilarPérez González, AlexandreRiera, MelchorJarrin Vera, InmaculadaRivero-Juarez, AntonioRivero, AntonioAnti-HIV AgentsAcquired Immunodeficiency SyndromeHIV InfectionsPiperazinesPyridonesAlanineAmidesHeterocyclic Compounds, 3-RingAdultMaleHumansFemaleDrug CombinationsEmtricitabineTenofovirObjectives: The efficacy of BIC/FTC/TAF in HIV late presenters initiating antiretroviral therapy (ART) has not been sufficiently evaluated. Methods: 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 <200 cells/mm3 and/or AIDS-defining conditions between January 1st 2019 and November 30th 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 <50 cop/mL, and immunological recovery (IR) (secondary objective), defined as CD4 count >200 cells/mm3, at weeks 24 and 48 after initiation of ART. Results: 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 < 0.005). Conclusion: Our results suggest that BIC/FTC/TAF could be a preferred regimen as initial therapy in HIV late presenters because of its high effectiveness and good tolerability.ElsevierGilead Sciences (Spain)Ministerio de Sanidad (España)Plan Nacional de I+D+i (España)Unión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF)Instituto de Salud Carlos IIIUnión Europea. Comisión Europea. NextGenerationEUMinisterio de Ciencia e Innovación (España)Centro de Investigación Biomédica en Red - CIBERINFEC (Enfermedades Infecciosas)20242024-03-1820242024-01-0120242024-01-01research articlehttp://purl.org/coar/resource_type/c_2df8fbb1VoRhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleapplication/pdfapplication/pdfhttp://hdl.handle.net/20.500.12105/18995reponame:Repisaludinstname:Instituto de Salud Carlos III (ISCIII)Inglésengopen accesshttp://purl.org/coar/access_right/c_abf2Attribution-NonCommercial-NoDerivatives 4.0 Internacionalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessoai:repisalud.isciii.es:20.500.12105/189952026-06-12T12:43:37Z
dc.title.none.fl_str_mv Effectiveness and safety of bictegravir/emtricitabine/tenofovir alafenamide in HIV late presenters
title Effectiveness and safety of bictegravir/emtricitabine/tenofovir alafenamide in HIV late presenters
spellingShingle Effectiveness and safety of bictegravir/emtricitabine/tenofovir alafenamide in HIV late presenters
Corona, Diana
Anti-HIV Agents
Acquired Immunodeficiency Syndrome
HIV Infections
Piperazines
Pyridones
Alanine
Amides
Heterocyclic Compounds, 3-Ring
Adult
Male
Humans
Female
Drug Combinations
Emtricitabine
Tenofovir
title_short Effectiveness and safety of bictegravir/emtricitabine/tenofovir alafenamide in HIV late presenters
title_full Effectiveness and safety of bictegravir/emtricitabine/tenofovir alafenamide in HIV late presenters
title_fullStr Effectiveness and safety of bictegravir/emtricitabine/tenofovir alafenamide in HIV late presenters
title_full_unstemmed Effectiveness and safety of bictegravir/emtricitabine/tenofovir alafenamide in HIV late presenters
title_sort Effectiveness and safety of bictegravir/emtricitabine/tenofovir alafenamide in HIV late presenters
dc.creator.none.fl_str_mv Corona, Diana
Pérez-Valero, Ignacio
Camacho, Angela
Gutiérrez Liarte, Ángela
Montero-Alonso, Marta
Alemán, María Remedios
Ruiz-Seco, Pilar
Pérez González, Alexandre
Riera, Melchor
Jarrin Vera, Inmaculada
Rivero-Juarez, Antonio
Rivero, Antonio
author Corona, Diana
author_facet Corona, Diana
Pérez-Valero, Ignacio
Camacho, Angela
Gutiérrez Liarte, Ángela
Montero-Alonso, Marta
Alemán, María Remedios
Ruiz-Seco, Pilar
Pérez González, Alexandre
Riera, Melchor
Jarrin Vera, Inmaculada
Rivero-Juarez, Antonio
Rivero, Antonio
author_role author
author2 Pérez-Valero, Ignacio
Camacho, Angela
Gutiérrez Liarte, Ángela
Montero-Alonso, Marta
Alemán, María Remedios
Ruiz-Seco, Pilar
Pérez González, Alexandre
Riera, Melchor
Jarrin Vera, Inmaculada
Rivero-Juarez, Antonio
Rivero, Antonio
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Gilead Sciences (Spain)
Ministerio de Sanidad (España)
Plan Nacional de I+D+i (España)
Unión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF)
Instituto de Salud Carlos III
Unión Europea. Comisión Europea. NextGenerationEU
Ministerio de Ciencia e Innovación (España)
Centro de Investigación Biomédica en Red - CIBERINFEC (Enfermedades Infecciosas)

dc.subject.none.fl_str_mv Anti-HIV Agents
Acquired Immunodeficiency Syndrome
HIV Infections
Piperazines
Pyridones
Alanine
Amides
Heterocyclic Compounds, 3-Ring
Adult
Male
Humans
Female
Drug Combinations
Emtricitabine
Tenofovir
topic Anti-HIV Agents
Acquired Immunodeficiency Syndrome
HIV Infections
Piperazines
Pyridones
Alanine
Amides
Heterocyclic Compounds, 3-Ring
Adult
Male
Humans
Female
Drug Combinations
Emtricitabine
Tenofovir
description Objectives: The efficacy of BIC/FTC/TAF in HIV late presenters initiating antiretroviral therapy (ART) has not been sufficiently evaluated. Methods: 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 <200 cells/mm3 and/or AIDS-defining conditions between January 1st 2019 and November 30th 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 <50 cop/mL, and immunological recovery (IR) (secondary objective), defined as CD4 count >200 cells/mm3, at weeks 24 and 48 after initiation of ART. Results: 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 < 0.005). Conclusion: Our results suggest that BIC/FTC/TAF could be a preferred regimen as initial therapy in HIV late presenters because of its high effectiveness and good tolerability.
publishDate 2024
dc.date.none.fl_str_mv 2024
2024-03-18
2024
2024-01-01
2024
2024-01-01
dc.type.none.fl_str_mv research article
http://purl.org/coar/resource_type/c_2df8fbb1
VoR
http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.openaire.fl_str_mv info:eu-repo/semantics/article
format article
dc.identifier.none.fl_str_mv http://hdl.handle.net/20.500.12105/18995
url http://hdl.handle.net/20.500.12105/18995
dc.language.none.fl_str_mv Inglés
eng
language_invalid_str_mv Inglés
language eng
dc.rights.none.fl_str_mv open access
http://purl.org/coar/access_right/c_abf2
Attribution-NonCommercial-NoDerivatives 4.0 Internacional
http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.openaire.fl_str_mv info:eu-repo/semantics/openAccess
rights_invalid_str_mv open access
http://purl.org/coar/access_right/c_abf2
Attribution-NonCommercial-NoDerivatives 4.0 Internacional
http://creativecommons.org/licenses/by-nc-nd/4.0/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:Repisalud
instname:Instituto de Salud Carlos III (ISCIII)
instname_str Instituto de Salud Carlos III (ISCIII)
reponame_str Repisalud
collection Repisalud
repository.name.fl_str_mv
repository.mail.fl_str_mv
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