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Efficacy and Safety of Switching to the 2-Drug Regimen Dolutegravir/Lamivudine Versus Continuing a 3-or 4-Drug Regimen for Maintaining Virologic Suppression in Adults Living With Human Immunodeficiency Virus 1 (HIV-1): Week 48 Results From the Phase 3, No

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dc.contributor.author Llibre, Josep-M
dc.contributor.author Brites, Carlos
dc.contributor.author Cheng, Chien-Yu
dc.contributor.author Osiyemi, Olayemi
dc.contributor.author Galera, Carlos
dc.contributor.author Hocqueloux, Laurent
dc.contributor.author Maggiolo, Franco
dc.contributor.author Degen, Olaf
dc.contributor.author Taylor, Stephen
dc.contributor.author Blair, Elizabeth
dc.contributor.author Man, Choy
dc.contributor.author Wynne, Brian
dc.contributor.author Oyee, James
dc.contributor.author Underwood, Mark
dc.contributor.author Curtis, Lloyd
dc.contributor.author Bontempo, Gilda
dc.contributor.author van-Wyk, Jean
dc.date.accessioned 2025-11-19T15:37:25Z
dc.date.available 2025-11-19T15:37:25Z
dc.date.issued 2023-02
dc.identifier.citation Llibre JM, Brites C, Cheng CY, Osiyemi O, Galera C, Hocqueloux L, et al. Efficacy and Safety of Switching to the 2-Drug Regimen Dolutegravir/Lamivudine Versus Continuing a 3- or 4-Drug Regimen for Maintaining Virologic Suppression in Adults Living With Human Immunodeficiency Virus 1 (HIV-1): Week 48 Results From the Phase 3, Noninferiority SALSA Randomized Trial. Clinical Infectious Diseases. 18 de febrero de 2023;76(4):720-9.
dc.identifier.issn 1058-4838
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/21322
dc.description.abstract BACKGROUND: In TANGO, switching to dolutegravir/lamivudine (DTG/3TC) demonstrated long-term noninferior efficacy vs continuing tenofovir alafenamide-based regimens in treatment-experienced adults with HIV-1. The phase 3 SALSA study evaluated efficacy and safety of switching to DTG/3TC compared with continuing various 3-/4-drug current antiretroviral regimens (CARs). METHODS: Adults with HIV-1 RNA <50 copies/mL and no previous virologic failure were randomized (1:1, stratified by baseline third agent class) to switch to once-daily fixed-dose combination DTG/3TC or continue CAR (primary endpoint: proportion of participants with HIV-1 RNA ?50 copies/mL at week 48; Snapshot, intention-to-treat-exposed population, 5% noninferiority margin). RESULTS: Overall, 493 adults (39% women; 39% aged ?50 years; 19% African American/African heritage; 14% Asian) were randomized to switch to DTG/3TC (n = 246) or continue CAR (n = 247). At week 48, 1 (0.4%) participant in the DTG/3TC group and 3 (1.2%) in the CAR group had HIV-1 RNA ?50 copies/mL (Snapshot), demonstrating noninferiority (adjusted difference, -0.8%; 95% CI, -2.4%, .8%). Zero participants met confirmed virologic withdrawal criteria; therefore, no resistance testing was performed. Drug-related adverse events were more frequent with DTG/3TC (20%) than CAR (6%) through week 48 but comparable post-week 24 (5% vs 2%, respectively). Proximal tubular renal function and bone turnover biomarkers improved with DTG/3TC. Both groups had generally minimal changes in lipids and inflammatory biomarkers. CONCLUSIONS: Switching to DTG/3TC was noninferior to continuing CAR for maintaining virologic suppression at week 48 with no observed resistance, supporting the efficacy, good safety, and high barrier to resistance of DTG/3TC. CLINICAL TRIALS REGISTRATION: www.clinicaltrials.gov, NCT04021290.
dc.language.iso eng
dc.publisher OXFORD UNIV PRESS INC
dc.rights Atribución/Reconocimiento-NoComercial-SinDerivados 4.0 Internacional
dc.rights.uri https://creativecommons.org/licenses/by-nc-nd/4.0/ *
dc.subject.mesh Adult
dc.subject.mesh Humans
dc.subject.mesh Female
dc.subject.mesh Male
dc.subject.mesh Lamivudine/therapeutic use
dc.subject.mesh HIV-1
dc.subject.mesh Anti-HIV Agents/therapeutic use
dc.subject.mesh HIV Infections/drug therapy
dc.subject.mesh Heterocyclic Compounds, 3-Ring/therapeutic use
dc.subject.mesh RNA, Viral
dc.subject.mesh Biomarkers
dc.title Efficacy and Safety of Switching to the 2-Drug Regimen Dolutegravir/Lamivudine Versus Continuing a 3-or 4-Drug Regimen for Maintaining Virologic Suppression in Adults Living With Human Immunodeficiency Virus 1 (HIV-1): Week 48 Results From the Phase 3, No
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 35235656
dc.relation.publisherversion https://academic.oup.com/cid/article/76/4/720/6541246
dc.identifier.doi 10.1093/cid/ciac130
dc.journal.title Clinical Infectious Diseases
dc.identifier.essn 1537-6591


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