Cargando…
DOLAVI Real-Life Study of Dolutegravir Plus Lamivudine in Naive HIV-1 Patients (48 Weeks)
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 object...
Autores principales: | , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8951045/ https://www.ncbi.nlm.nih.gov/pubmed/35336931 http://dx.doi.org/10.3390/v14030524 |
_version_ | 1784675289342672896 |
---|---|
author | Hidalgo-Tenorio, Carmen Pasquau, Juan Vinuesa, David Ferra, Sergio Terrón, Alberto SanJoaquín, Isabel Payeras, Antoni Martínez, Onofre Juan López-Ruz, Miguel Ángel Omar, Mohamed de la Torre-Lima, Javier López-Lirola, Ana Palomares, Jesús Blanco, José Ramón Montero, Marta García-Vallecillos, Coral |
author_facet | Hidalgo-Tenorio, Carmen Pasquau, Juan Vinuesa, David Ferra, Sergio Terrón, Alberto SanJoaquín, Isabel Payeras, Antoni Martínez, Onofre Juan López-Ruz, Miguel Ángel Omar, Mohamed de la Torre-Lima, Javier López-Lirola, Ana Palomares, Jesús Blanco, José Ramón Montero, Marta García-Vallecillos, Coral |
author_sort | Hidalgo-Tenorio, Carmen |
collection | PubMed |
description | 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 log(10), 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. |
format | Online Article Text |
id | pubmed-8951045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89510452022-03-26 DOLAVI Real-Life Study of Dolutegravir Plus Lamivudine in Naive HIV-1 Patients (48 Weeks) Hidalgo-Tenorio, Carmen Pasquau, Juan Vinuesa, David Ferra, Sergio Terrón, Alberto SanJoaquín, Isabel Payeras, Antoni Martínez, Onofre Juan López-Ruz, Miguel Ángel Omar, Mohamed de la Torre-Lima, Javier López-Lirola, Ana Palomares, Jesús Blanco, José Ramón Montero, Marta García-Vallecillos, Coral Viruses Article 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 log(10), 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. MDPI 2022-03-04 /pmc/articles/PMC8951045/ /pubmed/35336931 http://dx.doi.org/10.3390/v14030524 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Hidalgo-Tenorio, Carmen Pasquau, Juan Vinuesa, David Ferra, Sergio Terrón, Alberto SanJoaquín, Isabel Payeras, Antoni Martínez, Onofre Juan López-Ruz, Miguel Ángel Omar, Mohamed de la Torre-Lima, Javier López-Lirola, Ana Palomares, Jesús Blanco, José Ramón Montero, Marta García-Vallecillos, Coral DOLAVI Real-Life Study of Dolutegravir Plus Lamivudine in Naive HIV-1 Patients (48 Weeks) |
title | DOLAVI Real-Life Study of Dolutegravir Plus Lamivudine in Naive HIV-1 Patients (48 Weeks) |
title_full | DOLAVI Real-Life Study of Dolutegravir Plus Lamivudine in Naive HIV-1 Patients (48 Weeks) |
title_fullStr | DOLAVI Real-Life Study of Dolutegravir Plus Lamivudine in Naive HIV-1 Patients (48 Weeks) |
title_full_unstemmed | DOLAVI Real-Life Study of Dolutegravir Plus Lamivudine in Naive HIV-1 Patients (48 Weeks) |
title_short | DOLAVI Real-Life Study of Dolutegravir Plus Lamivudine in Naive HIV-1 Patients (48 Weeks) |
title_sort | dolavi real-life study of dolutegravir plus lamivudine in naive hiv-1 patients (48 weeks) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8951045/ https://www.ncbi.nlm.nih.gov/pubmed/35336931 http://dx.doi.org/10.3390/v14030524 |
work_keys_str_mv | AT hidalgotenoriocarmen dolavireallifestudyofdolutegravirpluslamivudineinnaivehiv1patients48weeks AT pasquaujuan dolavireallifestudyofdolutegravirpluslamivudineinnaivehiv1patients48weeks AT vinuesadavid dolavireallifestudyofdolutegravirpluslamivudineinnaivehiv1patients48weeks AT ferrasergio dolavireallifestudyofdolutegravirpluslamivudineinnaivehiv1patients48weeks AT terronalberto dolavireallifestudyofdolutegravirpluslamivudineinnaivehiv1patients48weeks AT sanjoaquinisabel dolavireallifestudyofdolutegravirpluslamivudineinnaivehiv1patients48weeks AT payerasantoni dolavireallifestudyofdolutegravirpluslamivudineinnaivehiv1patients48weeks AT martinezonofrejuan dolavireallifestudyofdolutegravirpluslamivudineinnaivehiv1patients48weeks AT lopezruzmiguelangel dolavireallifestudyofdolutegravirpluslamivudineinnaivehiv1patients48weeks AT omarmohamed dolavireallifestudyofdolutegravirpluslamivudineinnaivehiv1patients48weeks AT delatorrelimajavier dolavireallifestudyofdolutegravirpluslamivudineinnaivehiv1patients48weeks AT lopezlirolaana dolavireallifestudyofdolutegravirpluslamivudineinnaivehiv1patients48weeks AT palomaresjesus dolavireallifestudyofdolutegravirpluslamivudineinnaivehiv1patients48weeks AT blancojoseramon dolavireallifestudyofdolutegravirpluslamivudineinnaivehiv1patients48weeks AT monteromarta dolavireallifestudyofdolutegravirpluslamivudineinnaivehiv1patients48weeks AT garciavallecilloscoral dolavireallifestudyofdolutegravirpluslamivudineinnaivehiv1patients48weeks |