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Long-term outcome of lamivudine/dolutegravir dual therapy in HIV-infected, virologically suppressed patients

BACKGROUND: The use of DTG-containing two-drug regimens is one of the most promising solutions to the need to ease the management of HIV treatment without harming its efficacy and safety. We report long- term results in patients switched, while virologically suppressed, to the combination of doluteg...

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Autores principales: Maggiolo, Franco, Gulminetti, Roberto, Pagnucco, Layla, Digaetano, Margherita, Cervo, Adriana, Valenti, Daniela, Callegaro, Annapaola, Mussini, Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9558382/
https://www.ncbi.nlm.nih.gov/pubmed/36224538
http://dx.doi.org/10.1186/s12879-022-07769-6
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author Maggiolo, Franco
Gulminetti, Roberto
Pagnucco, Layla
Digaetano, Margherita
Cervo, Adriana
Valenti, Daniela
Callegaro, Annapaola
Mussini, Cristina
author_facet Maggiolo, Franco
Gulminetti, Roberto
Pagnucco, Layla
Digaetano, Margherita
Cervo, Adriana
Valenti, Daniela
Callegaro, Annapaola
Mussini, Cristina
author_sort Maggiolo, Franco
collection PubMed
description BACKGROUND: The use of DTG-containing two-drug regimens is one of the most promising solutions to the need to ease the management of HIV treatment without harming its efficacy and safety. We report long- term results in patients switched, while virologically suppressed, to the combination of dolutegravir (DTG) plus lamivudine (3TC). METHODS: This is a prospective, clinical, uncontrolled cohort enrolling ART-experienced people living with HIV (PLWH) with HIV-RNA < 50 copies/ml for 6 months or longer, negative hepatitis B virus surface antigen, and without known M184V/I mutations. Kaplan-Meiers curves are used to describe persistency of virological suppression on therapy and a Cox regression model to evaluate baseline characteristics and the risk of stopping therapy. RESULTS: 218 individuals switched their regimen since 2015. The mean estimated follow-up was of 64.3 months (95% CI 61.3–67.3) for approximately 1000 patient/years. After 5 years of follow-up, 77.1% were still on the DTG-3TC combination. No virologic failure was detected throughout the whole study period, and only 15 subjects presented single isolated viral blips above 50 copies/ml. Most patients stopped therapy because of reasons unrelated to study drugs (lost to follow-up; patients’ decision; moved to other Centers), but due to the unselected nature of the casuistry; 11 subjects died in the 5 years of follow-up mostly because of pre-existing co-morbidities (6 neoplastic diseases and 2 end-stage liver disease). The median baseline CD4 count was 669 cells/mcl (IQR 483–927). After 5 years it raised to 899 cells/mcl (IQR 646–1160) (P < 0.001) without a significant change of CD8 counts that lowered from 767 cells/mcl (IQR 532–1034) to 683 cells/mcl (IQR 538–988). Consequently, the CD4/CD8 ratio varied from 0.93 (IQR 0.60–1.30) to 1.15 (IQR 0.77–1.45) (P < 0.0001). A non-significant (P = 0.320) increment of mean creatinine, 0.06 mg/dl in magnitude, was observed over the whole follow-up. CONCLUSION: These long-term results over 5 years reinforce the durability and good tolerability of DTG-3TC. Our results continue to support the recommended switch use of this 2DR as a well-accepted treatment option for ART-experienced PLWH.
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spelling pubmed-95583822022-10-14 Long-term outcome of lamivudine/dolutegravir dual therapy in HIV-infected, virologically suppressed patients Maggiolo, Franco Gulminetti, Roberto Pagnucco, Layla Digaetano, Margherita Cervo, Adriana Valenti, Daniela Callegaro, Annapaola Mussini, Cristina BMC Infect Dis Research BACKGROUND: The use of DTG-containing two-drug regimens is one of the most promising solutions to the need to ease the management of HIV treatment without harming its efficacy and safety. We report long- term results in patients switched, while virologically suppressed, to the combination of dolutegravir (DTG) plus lamivudine (3TC). METHODS: This is a prospective, clinical, uncontrolled cohort enrolling ART-experienced people living with HIV (PLWH) with HIV-RNA < 50 copies/ml for 6 months or longer, negative hepatitis B virus surface antigen, and without known M184V/I mutations. Kaplan-Meiers curves are used to describe persistency of virological suppression on therapy and a Cox regression model to evaluate baseline characteristics and the risk of stopping therapy. RESULTS: 218 individuals switched their regimen since 2015. The mean estimated follow-up was of 64.3 months (95% CI 61.3–67.3) for approximately 1000 patient/years. After 5 years of follow-up, 77.1% were still on the DTG-3TC combination. No virologic failure was detected throughout the whole study period, and only 15 subjects presented single isolated viral blips above 50 copies/ml. Most patients stopped therapy because of reasons unrelated to study drugs (lost to follow-up; patients’ decision; moved to other Centers), but due to the unselected nature of the casuistry; 11 subjects died in the 5 years of follow-up mostly because of pre-existing co-morbidities (6 neoplastic diseases and 2 end-stage liver disease). The median baseline CD4 count was 669 cells/mcl (IQR 483–927). After 5 years it raised to 899 cells/mcl (IQR 646–1160) (P < 0.001) without a significant change of CD8 counts that lowered from 767 cells/mcl (IQR 532–1034) to 683 cells/mcl (IQR 538–988). Consequently, the CD4/CD8 ratio varied from 0.93 (IQR 0.60–1.30) to 1.15 (IQR 0.77–1.45) (P < 0.0001). A non-significant (P = 0.320) increment of mean creatinine, 0.06 mg/dl in magnitude, was observed over the whole follow-up. CONCLUSION: These long-term results over 5 years reinforce the durability and good tolerability of DTG-3TC. Our results continue to support the recommended switch use of this 2DR as a well-accepted treatment option for ART-experienced PLWH. BioMed Central 2022-10-12 /pmc/articles/PMC9558382/ /pubmed/36224538 http://dx.doi.org/10.1186/s12879-022-07769-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Maggiolo, Franco
Gulminetti, Roberto
Pagnucco, Layla
Digaetano, Margherita
Cervo, Adriana
Valenti, Daniela
Callegaro, Annapaola
Mussini, Cristina
Long-term outcome of lamivudine/dolutegravir dual therapy in HIV-infected, virologically suppressed patients
title Long-term outcome of lamivudine/dolutegravir dual therapy in HIV-infected, virologically suppressed patients
title_full Long-term outcome of lamivudine/dolutegravir dual therapy in HIV-infected, virologically suppressed patients
title_fullStr Long-term outcome of lamivudine/dolutegravir dual therapy in HIV-infected, virologically suppressed patients
title_full_unstemmed Long-term outcome of lamivudine/dolutegravir dual therapy in HIV-infected, virologically suppressed patients
title_short Long-term outcome of lamivudine/dolutegravir dual therapy in HIV-infected, virologically suppressed patients
title_sort long-term outcome of lamivudine/dolutegravir dual therapy in hiv-infected, virologically suppressed patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9558382/
https://www.ncbi.nlm.nih.gov/pubmed/36224538
http://dx.doi.org/10.1186/s12879-022-07769-6
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