Cargando…

554. Does Protease Inhibitor (PI) Monotherapy Select Primary PI Resistance?

BACKGROUND: Combination drug therapy is the standard of care for HIV treatment. PI monotherapy is considered experimental in the United States. However, some patients end up receiving PI monotherapy secondary to resistance and/or drug intolerance to other antiretroviral (cART) classes. This study wi...

Descripción completa

Detalles Bibliográficos
Autores principales: Saling, Christopher, Atallah, Liana, Haddad, Tyler, Learned, Brooke, Slim, Jihad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253806/
http://dx.doi.org/10.1093/ofid/ofy210.562
_version_ 1783373578904797184
author Saling, Christopher
Atallah, Liana
Haddad, Tyler
Learned, Brooke
Slim, Jihad
author_facet Saling, Christopher
Atallah, Liana
Haddad, Tyler
Learned, Brooke
Slim, Jihad
author_sort Saling, Christopher
collection PubMed
description BACKGROUND: Combination drug therapy is the standard of care for HIV treatment. PI monotherapy is considered experimental in the United States. However, some patients end up receiving PI monotherapy secondary to resistance and/or drug intolerance to other antiretroviral (cART) classes. This study will discuss real-life clinical results in patients on PI monotherapy and examine the potential for the development of primary PI mutations. METHODS: An observational retrospective study conducted in an inner-city HIV clinic identified 10 patients on PI monotherapy who each had two GenoSure Archive® (Labcorp) resistance profiles performed. Gender, race, prior cART, and baseline VL and CD4+ count were captured. VL and CD4+ count were trended in the time period between resistance tests. These profiles were then compared checking for the emergence of new primary PI mutations. RESULTS: Seven out of 10 patients were African American, two were Hispanic, one was Caucasian, and half were male. The mean time interval between archived resistance tests was 6.87 months. During the time between resistance profiles, nine were on darunavir and one switched from lopinavir to darunavir for less pill burden. Eight had an undetectable VL (defined by <50 copies/mL) at the first resistance test, seven had undetectable VL at the second resistance test, and six remained undetectable over the entire period between profiles. There were three that demonstrated blips in VL and one that experienced virological failure between the two sets of resistance tests. One patient had an initial resistance profile showing primary resistance to lopinavir. No patients gained any primary PI mutations to darunavir. CONCLUSION: The results of this study suggest that mainly darunavir-based PI monotherapy has good genetic barrier, even in the setting of virological failure. Larger studies examining similar data over longer durations are needed to confirm this finding. DISCLOSURES: All authors: No reported disclosures.
format Online
Article
Text
id pubmed-6253806
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-62538062018-11-28 554. Does Protease Inhibitor (PI) Monotherapy Select Primary PI Resistance? Saling, Christopher Atallah, Liana Haddad, Tyler Learned, Brooke Slim, Jihad Open Forum Infect Dis Abstracts BACKGROUND: Combination drug therapy is the standard of care for HIV treatment. PI monotherapy is considered experimental in the United States. However, some patients end up receiving PI monotherapy secondary to resistance and/or drug intolerance to other antiretroviral (cART) classes. This study will discuss real-life clinical results in patients on PI monotherapy and examine the potential for the development of primary PI mutations. METHODS: An observational retrospective study conducted in an inner-city HIV clinic identified 10 patients on PI monotherapy who each had two GenoSure Archive® (Labcorp) resistance profiles performed. Gender, race, prior cART, and baseline VL and CD4+ count were captured. VL and CD4+ count were trended in the time period between resistance tests. These profiles were then compared checking for the emergence of new primary PI mutations. RESULTS: Seven out of 10 patients were African American, two were Hispanic, one was Caucasian, and half were male. The mean time interval between archived resistance tests was 6.87 months. During the time between resistance profiles, nine were on darunavir and one switched from lopinavir to darunavir for less pill burden. Eight had an undetectable VL (defined by <50 copies/mL) at the first resistance test, seven had undetectable VL at the second resistance test, and six remained undetectable over the entire period between profiles. There were three that demonstrated blips in VL and one that experienced virological failure between the two sets of resistance tests. One patient had an initial resistance profile showing primary resistance to lopinavir. No patients gained any primary PI mutations to darunavir. CONCLUSION: The results of this study suggest that mainly darunavir-based PI monotherapy has good genetic barrier, even in the setting of virological failure. Larger studies examining similar data over longer durations are needed to confirm this finding. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2018-11-26 /pmc/articles/PMC6253806/ http://dx.doi.org/10.1093/ofid/ofy210.562 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Saling, Christopher
Atallah, Liana
Haddad, Tyler
Learned, Brooke
Slim, Jihad
554. Does Protease Inhibitor (PI) Monotherapy Select Primary PI Resistance?
title 554. Does Protease Inhibitor (PI) Monotherapy Select Primary PI Resistance?
title_full 554. Does Protease Inhibitor (PI) Monotherapy Select Primary PI Resistance?
title_fullStr 554. Does Protease Inhibitor (PI) Monotherapy Select Primary PI Resistance?
title_full_unstemmed 554. Does Protease Inhibitor (PI) Monotherapy Select Primary PI Resistance?
title_short 554. Does Protease Inhibitor (PI) Monotherapy Select Primary PI Resistance?
title_sort 554. does protease inhibitor (pi) monotherapy select primary pi resistance?
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253806/
http://dx.doi.org/10.1093/ofid/ofy210.562
work_keys_str_mv AT salingchristopher 554doesproteaseinhibitorpimonotherapyselectprimarypiresistance
AT atallahliana 554doesproteaseinhibitorpimonotherapyselectprimarypiresistance
AT haddadtyler 554doesproteaseinhibitorpimonotherapyselectprimarypiresistance
AT learnedbrooke 554doesproteaseinhibitorpimonotherapyselectprimarypiresistance
AT slimjihad 554doesproteaseinhibitorpimonotherapyselectprimarypiresistance