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Clinical outcomes of dolutegravir treatment in people living with HIV in Brazil: protocol for the CODE cohort

dc.contributor.authorBrites, Carlos
dc.contributor.authorLuz, Estela
dc.contributor.authorStelitano, Cristiani
dc.contributor.authorBahia, Fabianna
dc.contributor.authorde Lacerda, Marcus Vinícius Guimarães
dc.contributor.authorRamalho, Aline
dc.contributor.authorCardoso, Sandra Wagner
dc.contributor.authorMadruga, Valdez
dc.contributor.authorReuter, Tânia
dc.contributor.authorBarbosa, Alexandre Naime [UNESP]
dc.contributor.authorSperhack, Rosa Dea
dc.contributor.authorBay, Monica Baumgardt
dc.contributor.authorNewman, Tâmara
dc.contributor.authorMorejon, Karen
dc.contributor.authorPatelli, Maria
dc.contributor.authorLeal, Fábio
dc.contributor.authorSprinz, Eduardo
dc.contributor.authorMurray-Krezan, Cristina
dc.contributor.authorCarmody, Mary
dc.contributor.authorAnderson, Jess
dc.contributor.authorAragon, Alejandro
dc.contributor.authorChase, Benjamin
dc.contributor.authorZajdenverg, Roberto
dc.contributor.authorJones, Bryn
dc.contributor.authorDutra, Fatima
dc.contributor.authorPage, Kimberly
dc.date.accessioned2026-06-08T13:54:31Z
dc.date.issued2025-10-08
dc.description.abstractThe Clinical Outcomes of Dolutegravir Treatment in People Living with HIV in Brazil (CODE) cohort study is a multicenter, prospective, observational study designed to evaluate the safety and efficacy of Dolutegravir (DTG)-based antiretroviral therapy (ART) among people living with HIV across diverse settings in Brazil. With the recent global shift towards DTG as a preferred option for first-line ART, particularly in low- and middle-income countries, there is vital need for comprehensive real-world data to inform its widespread use. CODE aims to fill this knowledge gap by assessing the clinical outcomes of both ART-naïve and ART-experienced patients initiating DTG-based regimens, as well as those who have switched from non-DTG-based ART. The primary objective of this study is to determine the proportion of patients who discontinue DTG due to any adverse events, specifically focusing on metabolic and psychiatric outcomes. Secondary objectives include evaluating the rates of virological suppression, the occurrence of immune reconstitution inflammatory syndrome (IRIS), changes in body mass index (BMI), and the development of HIV drug resistance. The CODE cohort will enroll approximately 5000 participants from multiple clinical sites across Brazil, including 2500 ART-naïve individuals, 1000 patients switching to DTG-based regimens for various reasons, and a comparator group of 1500 individuals who initiated non-DTG-based ART between 2013 and 2016, before DTG was available in the country. Participants will be followed for up to 36 months, with data collection points at baseline, 6, 12, 24, and 36 months. This study is expected to generate critical insights into the long-term outcomes associated with DTG-based ART, particularly in real-world settings that reflect the complexities of routine clinical care. By providing robust data on the effectiveness and safety of DTG in a diverse patient population, the CODE study aims to contribute to the optimization of HIV treatment strategies both in Brazil and globally.Key words: HIV-1, Dolutegravir, Outcomes, Brazil
dc.description.affiliationUniversidade Federal da Bahia/Fundação Bahiana de Infectologia, Salvador, Bahia, Brazil
dc.description.affiliationCentro Estadual Especializado em Diagnóstico Assistência e Pesquisa, Bahia, Brazil
dc.description.affiliationFundação de Medicina Tropical Tropical do Amazonas, Manaus, Amazonas, Brazil
dc.description.affiliationHospital Geral de Nova Iguaçu, Rio de Janeiro, Brazil
dc.description.affiliationInstituto Nacional de Infectologia Evandro Chagas, Rio de Janeiro, Brazil
dc.description.affiliationCentro de Referência e Tratamento DST/AIDS, São Paulo, Brazil
dc.description.affiliationHospital Universitário Cassiano Antônio de Moraes, Espirito Santo, Brazil
dc.description.affiliationFaculdade de Medicina de Botucatu, Universidade Estadual Paulista, São Paulo, Brazil
dc.description.affiliationFundação Universidade de Caxias do Sul, Caxias do Sul, Rio Grande do Sul, Brazil
dc.description.affiliationDepartamento de Infectologia, Universidade Federal do Rio Grande do Norte, Natal, Brazil
dc.description.affiliationInstituto de Infectologia Emílio Ribas, São Paulo, Brazil
dc.description.affiliationHospital das Clínicas da Faculdade de Medicina de Ribeirao Preto, Universidade São Paulo, São Paulo, Brazil
dc.description.affiliationSociedade Campineira de Educação e Instrução, São Paulo, Brazil
dc.description.affiliationUniversidade Municipal de São Caetano do Sul, São Paulo, Brazil
dc.description.affiliationHospital de Clínicas de Porto Alegre, Porto Alegre, Rio Grande do Sul, Brazil
dc.description.affiliationDepartment of Medicine, University of Pittsburgh, Pittsburgh, PA, United States of America
dc.description.affiliationGillings School of Public Health, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States of America
dc.description.affiliationDepartment of Internal Medicine, University of New Mexico Health Sciences Scenter, Albuquerque, NM, United States of America
dc.description.affiliationGSK Brazil, Rio de Janeiro, Brazil
dc.description.affiliationViiV Healthcare, London, UK
dc.description.affiliationUnespFaculdade de Medicina de Botucatu, Universidade Estadual Paulista, São Paulo, Brazil
dc.identifierhttps://app.dimensions.ai/details/publication/pub.1193702808
dc.identifier.dimensionspub.1193702808
dc.identifier.doi10.1186/s12879-025-11700-0
dc.identifier.issn1471-2334
dc.identifier.orcid0000-0002-1062-7179
dc.identifier.orcid0000-0002-2187-4722
dc.identifier.orcid0000-0002-5569-1756
dc.identifier.orcid0000-0003-1986-3765
dc.identifier.orcid0000-0003-4343-8304
dc.identifier.orcid0000-0002-5488-1080
dc.identifier.orcid0009-0000-8117-9185
dc.identifier.orcid0000-0001-9296-367X
dc.identifier.orcid0000-0001-5230-0003
dc.identifier.orcid0000-0003-0977-4507
dc.identifier.orcid0000-0003-3374-9985
dc.identifier.orcid0000-0002-4673-6991
dc.identifier.pmcidPMC12505586
dc.identifier.pmid41062955
dc.identifier.urihttps://hdl.handle.net/11449/325176
dc.publisherSpringer Nature
dc.relation.ispartofBMC Infectious Diseases; n. 1; v. 25; p. 1248
dc.rights.accessRightsAcesso abertopt
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dc.rights.sourceRightsgold
dc.sourceDimensions
dc.titleClinical outcomes of dolutegravir treatment in people living with HIV in Brazil: protocol for the CODE cohort
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationa3cdb24b-db92-40d9-b3af-2eacecf9f2ba
relation.isOrgUnitOfPublication.latestForDiscoverya3cdb24b-db92-40d9-b3af-2eacecf9f2ba
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt

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