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DOLAVI Real-Life Study of Dolutegravir Plus Lamivudine in Naive HIV-1 Patients (48 Weeks)

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dc.contributor.author Hidalgo-Tenorio, Carmen
dc.contributor.author Pasquau, Juan
dc.contributor.author Vinuesa, David
dc.contributor.author Ferra, Sergio
dc.contributor.author Terron, Alberto
dc.contributor.author SanJoaquin, Isabel
dc.contributor.author Payeras, Antoni
dc.contributor.author Juan-Martínez, Onofre
dc.contributor.author López-Ruz, Miguel-Ángel
dc.contributor.author Omar, Mohamed
dc.contributor.author de-la-Torre-Lima, Javier
dc.contributor.author López-Lirola, Ana
dc.contributor.author Palomares, Jesús
dc.contributor.author Blanco, José-Ramón
dc.contributor.author Montero, Marta
dc.contributor.author García-Vallecillos, Coral
dc.date.accessioned 2025-11-26T11:36:12Z
dc.date.available 2025-11-26T11:36:12Z
dc.date.issued 2022-03
dc.identifier.citation Hidalgo-Tenorio C, Pasquau J, Vinuesa D, Ferra S, Terrón A, SanJoaquín I, et al. DOLAVI Real-Life Study of Dolutegravir Plus Lamivudine in Naive HIV-1 Patients (48 Weeks). Viruses. 4 de marzo de 2022;14(3):524.
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/22566
dc.description.abstract Brief: Real-world data in naïve HIV-1 patients demonstrate that dolutegravir plus lamivudine in a multiple tablet regimen is effective, safe, and satisfactory; it causes moderately increasing weight and abdominal circumference and is administrable on a test-and-treat strategy. Background: Our objectives were to determine the real-life effectiveness and safety of DT with dolutegravir (50 mg/QD) plus lamivudine (300 mg/QD) in a multiple-tablet regimen (MTR) in naïve PLHIV followed up for 48 weeks and to evaluate the compliance and satisfaction of patients. Material and methods: An open, single-arm, multicenter, non-randomized clinical trial from May 2019 through September 2020 with a 48-week follow-up. Results: The study included 88 PLHIV patients (87.5% male) with a mean age of 35.9 years; 76.1% were MSM patients. The mean baseline CD4 was 516.4 cells/uL, with a viral load (VL) of 4.49 log10, and 11.4% were in the AIDS stage. DT started within 7 days of first specialist consultation in all patients and the same day in 84.1%; 3.4% had baseline resistance mutations (K103N, V106I + E138A, and V108I); 12.5% were lost to follow-up. At week 48, 86.3% had VL < 50 cop/uL by intention-to-treat analysis and 98.7% by per-protocol (PP) analysis. Virological failure (VF) was recorded in 1.1%, with no resistance mutation. One blip was detected in 5.2% without VF. Three reported anxiety, dizziness, and cephalgia, respectively, at week 4 and one reported insomnia at week 24; none reported adverse events at week 48. The mean weight was 4 kg higher at 48 weeks (p = 0.0001) and abdominal circumference 3 cm larger at 24 weeks (p = 0.022). No forgetfulness occurred in 98.7% of patients. Patient satisfaction was 90/100 at 4, 24, and 48 weeks. Conclusion: Real-world data demonstrate that dolutegravir plus lamivudine in MTR is effective, safe, and satisfactory, moderately increasing weight and abdominal circumference and administrable on a test-and-treat strategy.
dc.language.iso eng
dc.publisher MDPI
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 Anti-HIV Agents/therapeutic use
dc.subject.mesh Drug Therapy, Combination
dc.subject.mesh Female
dc.subject.mesh HIV Infections/drug therapy
dc.subject.mesh HIV Seropositivity
dc.subject.mesh HIV-1/genetics
dc.subject.mesh Heterocyclic Compounds, 3-Ring/therapeutic use
dc.subject.mesh Homosexuality, Male
dc.subject.mesh Humans
dc.subject.mesh Lamivudine/therapeutic use
dc.subject.mesh Male
dc.subject.mesh Oxazines
dc.subject.mesh Piperazines
dc.subject.mesh Pyridones
dc.subject.mesh Sexual and Gender Minorities
dc.subject.mesh Viral Load
dc.title DOLAVI Real-Life Study of Dolutegravir Plus Lamivudine in Naive HIV-1 Patients (48 Weeks)
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 35336931
dc.relation.publisherversion https://www.mdpi.com/1999-4915/14/3/524
dc.identifier.doi 10.3390/v14030524
dc.journal.title Viruses-Basel
dc.identifier.essn 1999-4915


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Atribución/Reconocimiento-NoComercial-SinDerivados 4.0 Internacional Excepto si se señala otra cosa, la licencia del ítem se describe como Atribución/Reconocimiento-NoComercial-SinDerivados 4.0 Internacional

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