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Long-term virological suppression on first-line efavirenz + tenofovir + emtricitabine/lamivudine for HIV-1

OBJECTIVES: Evaluate long-term rates of virological failure and treatment interruption for people living with HIV (PLWHIV) with viral suppression on first-line efavirenz + tenofovir disoproxil fumarate + emtricitabine/lamivudine (EFV + TDF + FTC/3TC), and compare these according to patient character...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6410964/
https://www.ncbi.nlm.nih.gov/pubmed/30829745
http://dx.doi.org/10.1097/QAD.0000000000002126
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description OBJECTIVES: Evaluate long-term rates of virological failure and treatment interruption for people living with HIV (PLWHIV) with viral suppression on first-line efavirenz + tenofovir disoproxil fumarate + emtricitabine/lamivudine (EFV + TDF + FTC/3TC), and compare these according to patient characteristics. METHODS: PLWHIV enrolled in the Collaboration of Observational HIV Epidemiological Research Europe cohort collaboration, who started first-line EFV + TDF + FTC/3TC at age at least 16 years and had viral suppression (<200 copies/ml) within 9 months were included. Rates of virological failure (≥200 copies/ml) and (complete) treatment interruption were estimated according to years since initial suppression. We used Poisson regression to examine associations of baseline characteristics with rates of virological failure or treatment interruption. RESULTS: Among 19 527 eligible PLWHIV with median (interquartile range) follow-up 3.7 (2.0–5.6) years after initial viral suppression, the estimated rate of the combined incidence of virological failure or treatment interruption fell from 9.0/100 person-years in the first year to less than 4/100 person-years beyond 3 years from suppression; considering only those remaining on EFV + TDF + FTC/3TC, the combined rate dropped from 8.2/100 person-years in the first year to less than 3.5/100 person-years beyond 3 years. PLWHIV with injecting drug-related or heterosexual transmission were at higher risk of virological failure or treatment interruption, as were those of Black ethnicity. PLWHIV aged less than 35 years were at higher risk of virological failure and treatment interruption. CONCLUSION: PLWHIV starting first-line EFV + TDF + FTC/3TC had low rates of virological failure and treatment interruption up to 10 years from initial suppression. Demographic characteristics can be used to identify subpopulations with higher risks of these outcomes.
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spelling pubmed-64109642019-03-16 Long-term virological suppression on first-line efavirenz + tenofovir + emtricitabine/lamivudine for HIV-1 AIDS Concise Communication OBJECTIVES: Evaluate long-term rates of virological failure and treatment interruption for people living with HIV (PLWHIV) with viral suppression on first-line efavirenz + tenofovir disoproxil fumarate + emtricitabine/lamivudine (EFV + TDF + FTC/3TC), and compare these according to patient characteristics. METHODS: PLWHIV enrolled in the Collaboration of Observational HIV Epidemiological Research Europe cohort collaboration, who started first-line EFV + TDF + FTC/3TC at age at least 16 years and had viral suppression (<200 copies/ml) within 9 months were included. Rates of virological failure (≥200 copies/ml) and (complete) treatment interruption were estimated according to years since initial suppression. We used Poisson regression to examine associations of baseline characteristics with rates of virological failure or treatment interruption. RESULTS: Among 19 527 eligible PLWHIV with median (interquartile range) follow-up 3.7 (2.0–5.6) years after initial viral suppression, the estimated rate of the combined incidence of virological failure or treatment interruption fell from 9.0/100 person-years in the first year to less than 4/100 person-years beyond 3 years from suppression; considering only those remaining on EFV + TDF + FTC/3TC, the combined rate dropped from 8.2/100 person-years in the first year to less than 3.5/100 person-years beyond 3 years. PLWHIV with injecting drug-related or heterosexual transmission were at higher risk of virological failure or treatment interruption, as were those of Black ethnicity. PLWHIV aged less than 35 years were at higher risk of virological failure and treatment interruption. CONCLUSION: PLWHIV starting first-line EFV + TDF + FTC/3TC had low rates of virological failure and treatment interruption up to 10 years from initial suppression. Demographic characteristics can be used to identify subpopulations with higher risks of these outcomes. Lippincott Williams & Wilkins 2019-03-15 2019-01-03 /pmc/articles/PMC6410964/ /pubmed/30829745 http://dx.doi.org/10.1097/QAD.0000000000002126 Text en Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle Concise Communication
Long-term virological suppression on first-line efavirenz + tenofovir + emtricitabine/lamivudine for HIV-1
title Long-term virological suppression on first-line efavirenz + tenofovir + emtricitabine/lamivudine for HIV-1
title_full Long-term virological suppression on first-line efavirenz + tenofovir + emtricitabine/lamivudine for HIV-1
title_fullStr Long-term virological suppression on first-line efavirenz + tenofovir + emtricitabine/lamivudine for HIV-1
title_full_unstemmed Long-term virological suppression on first-line efavirenz + tenofovir + emtricitabine/lamivudine for HIV-1
title_short Long-term virological suppression on first-line efavirenz + tenofovir + emtricitabine/lamivudine for HIV-1
title_sort long-term virological suppression on first-line efavirenz + tenofovir + emtricitabine/lamivudine for hiv-1
topic Concise Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6410964/
https://www.ncbi.nlm.nih.gov/pubmed/30829745
http://dx.doi.org/10.1097/QAD.0000000000002126