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Effectiveness and safety of bictegravir/emtricitabine/tenofovir alafenamide in HIV late presenters.
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, Inmaculada; Rivero-Juárez, Antonio; Rivero, Antonio.
Affiliation
  • Corona D; Department of Infectious Diseases, Hospital Universitario Reina Sofia, Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Universidad de Córdoba (UCO), Córdoba, Spain.
  • Pérez-Valero I; Department of Infectious Diseases, Hospital Universitario Reina Sofia, Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Universidad de Córdoba (UCO), Córdoba, Spain; CIBERINFEC, ISCIII - CIBER de Enfermedades Infecciosas, Instituto de Salud Carlos III, 28029 Madrid, Spain. Electr
  • Camacho A; Department of Infectious Diseases, Hospital Universitario Reina Sofia, Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Universidad de Córdoba (UCO), Córdoba, Spain; CIBERINFEC, ISCIII - CIBER de Enfermedades Infecciosas, Instituto de Salud Carlos III, 28029 Madrid, Spain.
  • Gutiérrez Liarte Á; Hospital Universitario de la Princesa. Madrid, Spain.
  • Montero-Alonso M; Hospital Universitario y Politécnico de La Fe. Valencia, Spain.
  • Alemán MR; Hospital Universitario de Canarias. Canarias, Spain.
  • Ruiz-Seco P; Servicio de Medicina Interna. Hospital Universitario Infanta Sofía. Madrid, Spain.
  • Pérez González A; Group of Virology and Pathogenesis, Galicia Sur Health Research Institute (IIS Galicia Sur), Internal Medicine Department, Vigo, Spain.
  • Riera M; Hospital Universitario Son Espases, Islas Baleares, Spain.
  • Jarrin I; CIBERINFEC, ISCIII - CIBER de Enfermedades Infecciosas, Instituto de Salud Carlos III, 28029 Madrid, Spain; National Center for Epidemiology, Institute of Health Carlos III, Madrid, Spain.
  • Rivero-Juárez A; Department of Infectious Diseases, Hospital Universitario Reina Sofia, Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Universidad de Córdoba (UCO), Córdoba, Spain; CIBERINFEC, ISCIII - CIBER de Enfermedades Infecciosas, Instituto de Salud Carlos III, 28029 Madrid, Spain.
  • Rivero A; Department of Infectious Diseases, Hospital Universitario Reina Sofia, Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Universidad de Córdoba (UCO), Córdoba, Spain; CIBERINFEC, ISCIII - CIBER de Enfermedades Infecciosas, Instituto de Salud Carlos III, 28029 Madrid, Spain.
Int J Antimicrob Agents ; 63(1): 107016, 2024 Jan.
Article in En | MEDLINE | ID: mdl-37890734
ABSTRACT

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.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Piperazines / Pyridones / HIV Infections / Acquired Immunodeficiency Syndrome / Anti-HIV Agents / Alanine / Tenofovir / Amides / Heterocyclic Compounds, 3-Ring Limits: Adult / Female / Humans / Male Language: En Journal: Int J Antimicrob Agents Year: 2024 Type: Article Affiliation country: Spain

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Piperazines / Pyridones / HIV Infections / Acquired Immunodeficiency Syndrome / Anti-HIV Agents / Alanine / Tenofovir / Amides / Heterocyclic Compounds, 3-Ring Limits: Adult / Female / Humans / Male Language: En Journal: Int J Antimicrob Agents Year: 2024 Type: Article Affiliation country: Spain