Publication:
Effectiveness and tolerability of dolutegravir and abacavir/lamivudine administered as two separate pills compared to their equivalent single‐tablet regimen in a multicentre cohort in Spain

dc.contributor.authorSuárez‐García, Inés
dc.contributor.authorAlejos, Belén
dc.contributor.authorRuiz-Alguero, Marta
dc.contributor.authorGarcía Yubero, Cristina
dc.contributor.authorMoreno, Cristina
dc.contributor.authorBernal, Enrique
dc.contributor.authorPérez‐Is, Laura
dc.contributor.authorZubero, Zuriñe
dc.contributor.authordeZárraga Fernández, Miguel Alberto
dc.contributor.authorSamperiz Abad, Gloria
dc.contributor.authorJarrin Vera, Inmaculada
dc.contributor.authorCohort of the Spanish HIV/AIDS Research Network (CoRIS)
dc.contributor.funderInstituto de Salud Carlos III
dc.contributor.funderUnión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF)
dc.contributor.funderRed de Investigación Cooperativa en Investigación en Sida (España)es_ES
dc.date.accessioned2022-04-19T13:05:52Z
dc.date.available2022-04-19T13:05:52Z
dc.date.issued2021
dc.description.abstractIntroduction: We aimed to assess the effectiveness and tolerability of dolutegravir (DTG), abacavir (ABC) and lamivudine (3TC) administered as branded STR (DTG/ABC/3TC) or as two separate pills (DTG and either branded ABC/3TC [DTG+(ABC/3TC)b] or generic ABC/3TC [DTG+(ABC/3TC)g]). Methods: We included individuals from the multicentre cohort of the Spanish HIV/AIDS Research Network (CoRIS) who received DTG/ABC/3TC, DTG+(ABC/3TC)b or DTG+(ABC/3TC)g during 2015 to 2018. We used multivariable logistic regression to compare the proportion of antiretroviral-naïve individuals who achieved viral suppression (VS) (viral load ≤50 copies/mL) at 24 weeks of initiating with DTG+(ABC/3TC)b or DTG+(ABC/3TC)g versus DTG/ABC/3TC. We also calculated the proportion of virologically suppressed individuals who maintained VS at 24 weeks after switching from DTG/ABC/3TC to DTG+(ABC/3TC)g. Results: During the study period, 829, 68 and 47 treatment-naïve individuals started treatment with DTG/ABC/3TC, DTG+(ABC/3TC)b or DTG+(ABC/3TC)g respectively. The proportions of individuals who changed their regimens due to side effects during the first 24 weeks were 3.7%, 4.4% and 6.4% respectively (p = 0.646). We did not find significant differences in VS at 24 weeks among individuals starting with DTG+(ABC/3TC)b or DTG+(ABC/3TC)g compared to those initiating with DTG/ABC/3TC. Among 177 virologically suppressed individuals who switched from DTG/ABC/3TC to DTG+(ABC/3TC)g, 170 (96.0%) maintained VS at 24 weeks. Conclusions: In naïve individuals, the effectiveness and tolerability at 24 weeks of DTG plus ABC/3TC administered as two separate pills, either as branded or generic ABC/3TC, was similar to the STR DTG/ABC/3TC. Switching the STR DTG/ABC/3TC to its separate components DTG+(ABC/3TC)g in virologically suppressed individuals did not seem to impair its effectiveness.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipThis study was funded by the Instituto de Salud Carlos III (EPY 115/18 and Acción Estratégica en Salud, PI17/00774) and co-funded by the European Regional Environment Fund, “A way to make Europe”. CoRIS is supported by the Instituto de Salud Carlos III through the Red Temática de Investigación Cooperativa en Sida (RD06/006, RD12/0017/0018 and RD16/0002/0006) as part of the Plan Nacional I+D+i and co-financed by Instituto de Salud Carlos III-Subdirección General de Evaluación and the Fondo Europeo de Desarrollo Regional (FEDER).es_ES
dc.format.number7es_ES
dc.format.pagee25758es_ES
dc.format.volume24es_ES
dc.identifier.citationJ Int AIDS Soc. 2021;24(7):e25758.es_ES
dc.identifier.doi10.1002/jia2.25758es_ES
dc.identifier.e-issn1758-2652es_ES
dc.identifier.issn1758-2652es_ES
dc.identifier.journalJournal of the International AIDS Societyes_ES
dc.identifier.pubmedID34291580es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/14114
dc.language.isoenges_ES
dc.publisherWiley
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/RD06/006es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/RD16/0002/0006es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/RD12/0017/0018es_ES
dc.relation.projectFISinfo:fis/Instituto de Salud Carlos III/Programa Estatal de Fomento de la Investigación Científica y Técnica de Excelencia/Subprograma Estatal de Generación de Conocimiento/PI17 - Proyectos de investigacion en salud (AES 2017). Modalidad proyectos en salud. (2017)/PI17/00774es_ES
dc.relation.projectFISinfo:eu-repo/grantAgreement/ES/EPY115/18es_ES
dc.relation.publisherversionhttps://doi.org/10.1002/jia2.25758es_ES
dc.repisalud.centroISCIII::Centro Nacional de Epidemiologíaes_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectHIV infectionses_ES
dc.subjectAntiretroviral therapyes_ES
dc.subjectCohort studieses_ES
dc.subjectGeneric drugses_ES
dc.subjectSingle-tablet regimenses_ES
dc.titleEffectiveness and tolerability of dolutegravir and abacavir/lamivudine administered as two separate pills compared to their equivalent single‐tablet regimen in a multicentre cohort in Spaines_ES
dc.typeresearch articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
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