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Dolutegravir/lamivudine as a first-line regimen in a test-and-treat setting for newly diagnosed people living with HIV
OBJECTIVES: Dolutegravir/lamivudine (DTG/3TC) is indicated for treatment-naive and experienced people with HIV; however, questions remain about its utility in a test-and-treat setting because of potential transmitted resistance and baseline hepatitis B virus (HBV) co-infection. We present feasibilit...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8462441/ https://www.ncbi.nlm.nih.gov/pubmed/34115650 http://dx.doi.org/10.1097/QAD.0000000000002979 |
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author | Rolle, Charlotte-Paige Berhe, Mezgebe Singh, Tulika Ortiz, Roberto Wurapa, Anson Ramgopal, Moti Leone, Peter A. Matthews, Jessica E. Dalessandro, Marybeth Underwood, Mark R. Angelis, Konstantinos Wynne, Brian R. Merrill, Deanna Nguyen, Christopher van Wyk, Jean Zolopa, Andrew R. |
author_facet | Rolle, Charlotte-Paige Berhe, Mezgebe Singh, Tulika Ortiz, Roberto Wurapa, Anson Ramgopal, Moti Leone, Peter A. Matthews, Jessica E. Dalessandro, Marybeth Underwood, Mark R. Angelis, Konstantinos Wynne, Brian R. Merrill, Deanna Nguyen, Christopher van Wyk, Jean Zolopa, Andrew R. |
author_sort | Rolle, Charlotte-Paige |
collection | PubMed |
description | OBJECTIVES: Dolutegravir/lamivudine (DTG/3TC) is indicated for treatment-naive and experienced people with HIV; however, questions remain about its utility in a test-and-treat setting because of potential transmitted resistance and baseline hepatitis B virus (HBV) co-infection. We present feasibility and efficacy of DTG/3TC in newly diagnosed individuals in a test-and-treat setting. DESIGN: The single-arm STAT study evaluated DTG/3TC in a US test-and-treat setting. METHODS: Eligible adults initiated DTG/3TC 14 days or less after HIV-1 diagnosis without availability of baseline laboratory results. If baseline testing indicated DTG or 3TC resistance, HBV co-infection, or creatinine clearance less than 30 ml/min per 1.73 m(2), participants remained on study with treatment modification. Efficacy endpoints included proportions of participants with HIV-1 RNA less than 50 copies/ml at Week 24, regardless of antiretroviral regimen, among all participants (intention-to-treat exposed) and those with available HIV-1 RNA data (observed). RESULTS: Of 131 participants enrolled, 8% were female and 50% were non-white. Through Week 24, treatment was modified in eight participants [five with HBV co-infection, one with baseline M184V, one for adverse event (rash), one participant decision]. At Week 24, 78% (102/131) of all participants and 92% (102/111) of those with available data achieved HIV-1 RNA less than 50 copies/ml. Incidence of drug-related adverse events was low (7%); no drug-related serious adverse events occurred. CONCLUSION: These data demonstrate the feasibility, efficacy, and safety of using DTG/3TC as a first-line regimen in a test-and-treat setting, with therapy adjustments for baseline resistance or HBV co-infection occurring safely via routine clinical care as needed [ClinicalTrials.gov, NCT03945981; see Supplemental Digital Content 1, video abstract (Video abstract summarizing the STAT study design and results)]. |
format | Online Article Text |
id | pubmed-8462441 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-84624412021-09-28 Dolutegravir/lamivudine as a first-line regimen in a test-and-treat setting for newly diagnosed people living with HIV Rolle, Charlotte-Paige Berhe, Mezgebe Singh, Tulika Ortiz, Roberto Wurapa, Anson Ramgopal, Moti Leone, Peter A. Matthews, Jessica E. Dalessandro, Marybeth Underwood, Mark R. Angelis, Konstantinos Wynne, Brian R. Merrill, Deanna Nguyen, Christopher van Wyk, Jean Zolopa, Andrew R. AIDS Clinical Science OBJECTIVES: Dolutegravir/lamivudine (DTG/3TC) is indicated for treatment-naive and experienced people with HIV; however, questions remain about its utility in a test-and-treat setting because of potential transmitted resistance and baseline hepatitis B virus (HBV) co-infection. We present feasibility and efficacy of DTG/3TC in newly diagnosed individuals in a test-and-treat setting. DESIGN: The single-arm STAT study evaluated DTG/3TC in a US test-and-treat setting. METHODS: Eligible adults initiated DTG/3TC 14 days or less after HIV-1 diagnosis without availability of baseline laboratory results. If baseline testing indicated DTG or 3TC resistance, HBV co-infection, or creatinine clearance less than 30 ml/min per 1.73 m(2), participants remained on study with treatment modification. Efficacy endpoints included proportions of participants with HIV-1 RNA less than 50 copies/ml at Week 24, regardless of antiretroviral regimen, among all participants (intention-to-treat exposed) and those with available HIV-1 RNA data (observed). RESULTS: Of 131 participants enrolled, 8% were female and 50% were non-white. Through Week 24, treatment was modified in eight participants [five with HBV co-infection, one with baseline M184V, one for adverse event (rash), one participant decision]. At Week 24, 78% (102/131) of all participants and 92% (102/111) of those with available data achieved HIV-1 RNA less than 50 copies/ml. Incidence of drug-related adverse events was low (7%); no drug-related serious adverse events occurred. CONCLUSION: These data demonstrate the feasibility, efficacy, and safety of using DTG/3TC as a first-line regimen in a test-and-treat setting, with therapy adjustments for baseline resistance or HBV co-infection occurring safely via routine clinical care as needed [ClinicalTrials.gov, NCT03945981; see Supplemental Digital Content 1, video abstract (Video abstract summarizing the STAT study design and results)]. Lippincott Williams & Wilkins 2021-10-01 2021-06-09 /pmc/articles/PMC8462441/ /pubmed/34115650 http://dx.doi.org/10.1097/QAD.0000000000002979 Text en Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Clinical Science Rolle, Charlotte-Paige Berhe, Mezgebe Singh, Tulika Ortiz, Roberto Wurapa, Anson Ramgopal, Moti Leone, Peter A. Matthews, Jessica E. Dalessandro, Marybeth Underwood, Mark R. Angelis, Konstantinos Wynne, Brian R. Merrill, Deanna Nguyen, Christopher van Wyk, Jean Zolopa, Andrew R. Dolutegravir/lamivudine as a first-line regimen in a test-and-treat setting for newly diagnosed people living with HIV |
title | Dolutegravir/lamivudine as a first-line regimen in a test-and-treat setting for newly diagnosed people living with HIV |
title_full | Dolutegravir/lamivudine as a first-line regimen in a test-and-treat setting for newly diagnosed people living with HIV |
title_fullStr | Dolutegravir/lamivudine as a first-line regimen in a test-and-treat setting for newly diagnosed people living with HIV |
title_full_unstemmed | Dolutegravir/lamivudine as a first-line regimen in a test-and-treat setting for newly diagnosed people living with HIV |
title_short | Dolutegravir/lamivudine as a first-line regimen in a test-and-treat setting for newly diagnosed people living with HIV |
title_sort | dolutegravir/lamivudine as a first-line regimen in a test-and-treat setting for newly diagnosed people living with hiv |
topic | Clinical Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8462441/ https://www.ncbi.nlm.nih.gov/pubmed/34115650 http://dx.doi.org/10.1097/QAD.0000000000002979 |
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