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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 |