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2060. Evaluation of the real world incidence of integrase inhibitor resistance since adoption as guideline preferred therapy
BACKGROUND: There are limited data reporting real-world incidence of integrase inhibitor resistance (INSTI-R) since the approval and first-line treatment recommendation of INSTIs in the US. A recent analysis of the national surveillance data estimated INSTI-R to be 6.3%. The purpose of this study wa...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9752527/ http://dx.doi.org/10.1093/ofid/ofac492.1682 |
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author | Januszka, Jenna Drwiega, Emily N Drwiega, Emily N Burgos, Rodrigo M Michienzi, Sarah M Smith, Renata Badowski, Melissa E |
author_facet | Januszka, Jenna Drwiega, Emily N Drwiega, Emily N Burgos, Rodrigo M Michienzi, Sarah M Smith, Renata Badowski, Melissa E |
author_sort | Januszka, Jenna |
collection | PubMed |
description | BACKGROUND: There are limited data reporting real-world incidence of integrase inhibitor resistance (INSTI-R) since the approval and first-line treatment recommendation of INSTIs in the US. A recent analysis of the national surveillance data estimated INSTI-R to be 6.3%. The purpose of this study was to describe real-world incidence of INSTI-R in patients who used an INSTI-based single tablet regimen (STR) in a major metropolitan area and identify risk factors for resistance. METHODS: This was a retrospective study of adult patients living with human immunodeficiency virus (HIV) who were prescribed an INSTI-STR between September 2017 and September 2020 and followed for > 12 months at the University of Illinois Chicago Community Clinic Network (UCCN). The primary endpoint was the difference in INSTI-R in UCCN patients compared to the national prevalence of 6.3%. Other outcomes included development of virologic failure (VF), defined as 2 consecutive HIV-1 viral loads (VL) > 200 copies/mL after week 24, and documented INSTI-R mutations. Patient specific factors associated with medication nonadherence were also collected. All endpoints were analyzed using chi-square and Fisher’s exact tests. RESULTS: Of 948 patients screened, 248 patients were included. Baseline characteristics are summarized in Table 1. VF occurred in 17 subjects (6.8%). Two of the 17 (11.8%) received subsequent INSTI-R testing and nine eventually virally suppressed without regimen changes (52.9%). Patients without VF were assumed to have no INSTI-R. No subjects developed INSTI-R, which was significantly less than the national prevalence of 6.3% (p=0.0029). Patients with a high VL at baseline were more likely to experience VF (p=0.001). The most common factors associated with nonadherence in patients with VF are summarized in Table 2. [Figure: see text] [Figure: see text] CONCLUSION: The true rate of INSTI-R in UCCN patients is still unknown and factors associated with developing INSTI-R were unable to be assessed. Among patients at UCCN on INSTI-based STRs, INSTI-R rates were lower than the national average. Future analyses should also include patients on INSTI-based non-STR regimens as increased pill burden is a known risk factor for nonadherence leading to VF and drug resistance. DISCLOSURES: All Authors: No reported disclosures. |
format | Online Article Text |
id | pubmed-9752527 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-97525272022-12-16 2060. Evaluation of the real world incidence of integrase inhibitor resistance since adoption as guideline preferred therapy Januszka, Jenna Drwiega, Emily N Drwiega, Emily N Burgos, Rodrigo M Michienzi, Sarah M Smith, Renata Badowski, Melissa E Open Forum Infect Dis Abstracts BACKGROUND: There are limited data reporting real-world incidence of integrase inhibitor resistance (INSTI-R) since the approval and first-line treatment recommendation of INSTIs in the US. A recent analysis of the national surveillance data estimated INSTI-R to be 6.3%. The purpose of this study was to describe real-world incidence of INSTI-R in patients who used an INSTI-based single tablet regimen (STR) in a major metropolitan area and identify risk factors for resistance. METHODS: This was a retrospective study of adult patients living with human immunodeficiency virus (HIV) who were prescribed an INSTI-STR between September 2017 and September 2020 and followed for > 12 months at the University of Illinois Chicago Community Clinic Network (UCCN). The primary endpoint was the difference in INSTI-R in UCCN patients compared to the national prevalence of 6.3%. Other outcomes included development of virologic failure (VF), defined as 2 consecutive HIV-1 viral loads (VL) > 200 copies/mL after week 24, and documented INSTI-R mutations. Patient specific factors associated with medication nonadherence were also collected. All endpoints were analyzed using chi-square and Fisher’s exact tests. RESULTS: Of 948 patients screened, 248 patients were included. Baseline characteristics are summarized in Table 1. VF occurred in 17 subjects (6.8%). Two of the 17 (11.8%) received subsequent INSTI-R testing and nine eventually virally suppressed without regimen changes (52.9%). Patients without VF were assumed to have no INSTI-R. No subjects developed INSTI-R, which was significantly less than the national prevalence of 6.3% (p=0.0029). Patients with a high VL at baseline were more likely to experience VF (p=0.001). The most common factors associated with nonadherence in patients with VF are summarized in Table 2. [Figure: see text] [Figure: see text] CONCLUSION: The true rate of INSTI-R in UCCN patients is still unknown and factors associated with developing INSTI-R were unable to be assessed. Among patients at UCCN on INSTI-based STRs, INSTI-R rates were lower than the national average. Future analyses should also include patients on INSTI-based non-STR regimens as increased pill burden is a known risk factor for nonadherence leading to VF and drug resistance. DISCLOSURES: All Authors: No reported disclosures. Oxford University Press 2022-12-15 /pmc/articles/PMC9752527/ http://dx.doi.org/10.1093/ofid/ofac492.1682 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Abstracts Januszka, Jenna Drwiega, Emily N Drwiega, Emily N Burgos, Rodrigo M Michienzi, Sarah M Smith, Renata Badowski, Melissa E 2060. Evaluation of the real world incidence of integrase inhibitor resistance since adoption as guideline preferred therapy |
title | 2060. Evaluation of the real world incidence of integrase inhibitor resistance since adoption as guideline preferred therapy |
title_full | 2060. Evaluation of the real world incidence of integrase inhibitor resistance since adoption as guideline preferred therapy |
title_fullStr | 2060. Evaluation of the real world incidence of integrase inhibitor resistance since adoption as guideline preferred therapy |
title_full_unstemmed | 2060. Evaluation of the real world incidence of integrase inhibitor resistance since adoption as guideline preferred therapy |
title_short | 2060. Evaluation of the real world incidence of integrase inhibitor resistance since adoption as guideline preferred therapy |
title_sort | 2060. evaluation of the real world incidence of integrase inhibitor resistance since adoption as guideline preferred therapy |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9752527/ http://dx.doi.org/10.1093/ofid/ofac492.1682 |
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