Durable Efficacy of Switching From a 3- or 4-Drug Tenofovir Alafenamide-Based Regimen to the 2-Drug Regimen Dolutegravir/Lamivudine in the TANGO Study Through Week 196
dc.rights.license | open | en_US |
dc.contributor.author | DE WIT, Stephane | |
hal.structure.identifier | Bordeaux population health [BPH] | |
hal.structure.identifier | Global Health in the Global South [GHiGS] | |
dc.contributor.author | BONNET, Fabrice | |
dc.contributor.author | OSIYEMI, Olayemi | |
dc.contributor.author | BISSHOP, Fiona | |
dc.contributor.author | OLALLA, Julian | |
dc.contributor.author | ROUTY, Jean-Pierre | |
dc.contributor.author | WYEN, Christoph | |
dc.contributor.author | MOODLEY, Riya | |
dc.contributor.author | PAPPA, Keith | |
dc.contributor.author | WANG, Ruolan | |
dc.contributor.author | OYEE, James | |
dc.contributor.author | SAGGU, Parminder | |
dc.contributor.author | LETANG, Emilio | |
dc.contributor.author | WYNNE, Brian | |
dc.contributor.author | JONES, Bryn | |
dc.contributor.author | SMITH, Kimberly Y | |
dc.contributor.author | AIT-KHALED, Mounir | |
dc.date.accessioned | 2024-05-02T11:13:24Z | |
dc.date.available | 2024-05-02T11:13:24Z | |
dc.date.issued | 2024-03-01 | |
dc.identifier.issn | 1944-7884 | en_US |
dc.identifier.uri | https://oskar-bordeaux.fr/handle/20.500.12278/199572 | |
dc.description.abstractEn | BACKGROUND: Switching to the 2-drug regimen dolutegravir/lamivudine demonstrated durable non-inferior efficacy vs continuing 3- or 4-drug tenofovir alafenamide-based regimens for maintaining virologic suppression in people with HIV-1 through Week 144 in TANGO. SETTING: 134 centers, 10 countries. METHODS: Adults with HIV-1 RNA <50 copies/mL for >6 months and no history of virologic failure were randomized to switch from stable tenofovir alafenamide-based regimens to dolutegravir/lamivudine on Day 1 (early-switch group) for 196 weeks. Those randomized to continue tenofovir alafenamide-based regimens on Day 1 who maintained virologic suppression at Week 144 switched to dolutegravir/lamivudine at Week 148 (late-switch group). Efficacy, safety, and tolerability (including weight and biomarker changes) of dolutegravir/lamivudine in early-switch and late-switch groups were assessed through Week 196. RESULTS: Overall, 369 participants switched to dolutegravir/lamivudine on Day 1 (early-switch) and 298 switched at Week 148 (late-switch). In the early-switch group, 83% (306/369) maintained virologic suppression through Year 4, and 3% (11/369) reported new adverse events between Weeks 144 and 196. The late-switch group at Week 196 and early-switch group at Week 48 had comparable proportions with virologic suppression (93% each) and similar safety profiles. No late-switch participants and 1 early-switch participant met confirmed virologic withdrawal criteria through Week 196, with no resistance-associated mutations observed. Treatment continued to be well tolerated long-term. CONCLUSION: Switching from tenofovir alafenamide-based regimens to dolutegravir/lamivudine showed durable efficacy, high barrier to resistance, and good tolerability through 4 years. These results support dolutegravir/lamivudine as a robust treatment for maintaining virologic suppression. | |
dc.language.iso | EN | en_US |
dc.rights | Attribution-NonCommercial-NoDerivs 3.0 United States | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/us/ | * |
dc.subject.en | Antiretroviral therapy | |
dc.subject.en | 2-drug regimen | |
dc.subject.en | Integrase strand transfer inhibitor | |
dc.title.en | Durable Efficacy of Switching From a 3- or 4-Drug Tenofovir Alafenamide-Based Regimen to the 2-Drug Regimen Dolutegravir/Lamivudine in the TANGO Study Through Week 196 | |
dc.title.alternative | J Acquir Immune Defic Syndr | en_US |
dc.type | Article de revue | en_US |
dc.identifier.doi | 10.1097/QAI.0000000000003395 | en_US |
dc.subject.hal | Sciences du Vivant [q-bio]/Santé publique et épidémiologie | en_US |
dc.identifier.pubmed | 38346427 | en_US |
bordeaux.journal | Journal of Acquired Immune Deficiency Syndromes - JAIDS | en_US |
bordeaux.hal.laboratories | Bordeaux Population Health Research Center (BPH) - UMR 1219 | en_US |
bordeaux.institution | Université de Bordeaux | en_US |
bordeaux.institution | INSERM | en_US |
bordeaux.team | GHIGS_BPH | en_US |
bordeaux.peerReviewed | oui | en_US |
bordeaux.inpress | non | en_US |
bordeaux.identifier.funderID | Institut de Recherche pour le Développement | en_US |
bordeaux.identifier.funderID | ViiV Healthcare | en_US |
hal.identifier | hal-04566132 | |
hal.version | 1 | |
hal.date.transferred | 2024-05-02T11:13:28Z | |
hal.popular | non | en_US |
hal.audience | Internationale | en_US |
hal.export | true | |
dc.rights.cc | Pas de Licence CC | en_US |
bordeaux.COinS | ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Journal%20of%20Acquired%20Immune%20Deficiency%20Syndromes%20-%20JAIDS&rft.date=2024-03-01&rft.eissn=1944-7884&rft.issn=1944-7884&rft.au=DE%20WIT,%20Stephane&BONNET,%20Fabrice&OSIYEMI,%20Olayemi&BISSHOP,%20Fiona&OLALLA,%20Julian&rft.genre=article |