Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/200633
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dc.contributor.authorWang, Ruolan-
dc.contributor.authorWright, Jonathan-
dc.contributor.authorSaggu, Parminder-
dc.contributor.authorAit-Khaled, Mounir-
dc.contributor.authorMoodley, Riya-
dc.contributor.authorParry, Chris M.-
dc.contributor.authorLutz, Thomas-
dc.contributor.authorPodzamczer Palter, Daniel-
dc.contributor.authorMoore, Richard-
dc.contributor.authorGórgolas Hernández-Mora, Miguel-
dc.contributor.authorKinder, Clifford-
dc.contributor.authorWynne, Brian-
dc.contributor.authorWyk, Jean van-
dc.contributor.authorUnderwood, Mark-
dc.date.accessioned2023-07-14T10:19:23Z-
dc.date.available2023-07-14T10:19:23Z-
dc.date.issued2023-06-11-
dc.identifier.issn1999-4915-
dc.identifier.urihttps://hdl.handle.net/2445/200633-
dc.description.abstractThe TANGO study (ClinicalTrials.gov, NCT03446573) demonstrated that switching to dolutegravir/lamivudine (DTG/3TC) was non-inferior to continuing tenofovir alafenamide-based regimens (TBR) through week 144. Retrospective baseline proviral DNA genotypes were performed for 734 participants (post-hoc analysis) to assess the impact of archived, pre-existing drug resistance on 144-week virologic outcomes by last on-treatment viral load (VL) and Snapshot. A total of 320 (86%) participants on DTG/3TC and 318 (85%) on TBR had both proviral genotype data and & GE;1 on-treatment post-baseline VL results and were defined as the proviral DNA resistance analysis population. Archived International AIDS Society-USA major nucleoside reverse transcriptase inhibitor, non-nucleoside reverse transcriptase inhibitor, protease inhibitor, and integrase strand transfer inhibitor resistance-associated mutations (RAMs) were observed in 42 (7%), 90 (14%), 42 (7%), and 11 (2%) participants, respectively, across both groups; 469 (74%) had no major RAMs at baseline. M184V/I (1%), K65N/R (<1%), and thymidine analogue mutations (2%) were infrequent. Through week 144, >99% of participants on DTG/3TC and 99% on TBR were virologically suppressed (last on-treatment VL <50 copies/mL) regardless of the presence of major RAMs. Results from the sensitivity analysis by Snapshot were consistent with the last available on-treatment VL. In TANGO, archived, pre-existing major RAMs did not impact virologic outcomes through week 144.-
dc.format.extent9 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherMDPI AG-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3390/v15061350-
dc.relation.ispartofViruses, 2023, vol. 15, num. 6-
dc.relation.urihttps://doi.org/10.3390/v15061350-
dc.rightscc by (c) Wang, Ruolan et al, 2023-
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))-
dc.subject.classificationPersones seropositives-
dc.subject.classificationAntiretrovirals-
dc.subject.otherHIV-positive persons-
dc.subject.otherAntiretroviral agents-
dc.titleAssessing the Virologic Impact of Archived Resistance in the Dolutegravir/Lamivudine 2-Drug Regimen HIV-1 Switch Study TANGO through Week 144-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.date.updated2023-07-13T09:00:56Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid37376649-
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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