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Modelling imperfect adherence to HIV induction therapy

BACKGROUND: Induction-maintenance therapy is a treatment regime where patients are prescribed an intense course of treatment for a short period of time (the induction phase), followed by a simplified long-term regimen (maintenance). Since induction therapy has a significantly higher chance of pill f...

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Autores principales: Miron, Rachelle E, Smith?, Robert J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2833165/
https://www.ncbi.nlm.nih.gov/pubmed/20064271
http://dx.doi.org/10.1186/1471-2334-10-6
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author Miron, Rachelle E
Smith?, Robert J
author_facet Miron, Rachelle E
Smith?, Robert J
author_sort Miron, Rachelle E
collection PubMed
description BACKGROUND: Induction-maintenance therapy is a treatment regime where patients are prescribed an intense course of treatment for a short period of time (the induction phase), followed by a simplified long-term regimen (maintenance). Since induction therapy has a significantly higher chance of pill fatigue than maintenance therapy, patients might take drug holidays during this period. Without guidance, patients who choose to stop therapy will each be making individual decisions, with no scientific basis. METHODS: We use mathematical modelling to investigate the effect of imperfect adherence during the inductive phase. We address the following research questions: 1. Can we theoretically determine the maximal length of a possible drug holiday and the minimal number of doses that must subsequently be taken while still avoiding resistance? 2. How many drug holidays can be taken during the induction phase? RESULTS: For a 180 day therapeutic program, a patient can take several drug holidays, but then has to follow each drug holiday with a strict, but fairly straightforward, drug-taking regimen. Since the results are dependent upon the drug regimen, we calculated the length and number of drug holidays for all fifteen protease-sparing triple-drug cocktails that have been approved by the US Food and Drug Administration. CONCLUSIONS: Induction therapy with partial adherence is tolerable, but the outcome depends on the drug cocktail. Our theoretical predictions are in line with recent results from pilot studies of short-cycle treatment interruption strategies and may be useful in guiding the design of future clinical trials.
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spelling pubmed-28331652010-03-06 Modelling imperfect adherence to HIV induction therapy Miron, Rachelle E Smith?, Robert J BMC Infect Dis Research Article BACKGROUND: Induction-maintenance therapy is a treatment regime where patients are prescribed an intense course of treatment for a short period of time (the induction phase), followed by a simplified long-term regimen (maintenance). Since induction therapy has a significantly higher chance of pill fatigue than maintenance therapy, patients might take drug holidays during this period. Without guidance, patients who choose to stop therapy will each be making individual decisions, with no scientific basis. METHODS: We use mathematical modelling to investigate the effect of imperfect adherence during the inductive phase. We address the following research questions: 1. Can we theoretically determine the maximal length of a possible drug holiday and the minimal number of doses that must subsequently be taken while still avoiding resistance? 2. How many drug holidays can be taken during the induction phase? RESULTS: For a 180 day therapeutic program, a patient can take several drug holidays, but then has to follow each drug holiday with a strict, but fairly straightforward, drug-taking regimen. Since the results are dependent upon the drug regimen, we calculated the length and number of drug holidays for all fifteen protease-sparing triple-drug cocktails that have been approved by the US Food and Drug Administration. CONCLUSIONS: Induction therapy with partial adherence is tolerable, but the outcome depends on the drug cocktail. Our theoretical predictions are in line with recent results from pilot studies of short-cycle treatment interruption strategies and may be useful in guiding the design of future clinical trials. BioMed Central 2010-01-12 /pmc/articles/PMC2833165/ /pubmed/20064271 http://dx.doi.org/10.1186/1471-2334-10-6 Text en Copyright ©2010 Miron and Smith?; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Miron, Rachelle E
Smith?, Robert J
Modelling imperfect adherence to HIV induction therapy
title Modelling imperfect adherence to HIV induction therapy
title_full Modelling imperfect adherence to HIV induction therapy
title_fullStr Modelling imperfect adherence to HIV induction therapy
title_full_unstemmed Modelling imperfect adherence to HIV induction therapy
title_short Modelling imperfect adherence to HIV induction therapy
title_sort modelling imperfect adherence to hiv induction therapy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2833165/
https://www.ncbi.nlm.nih.gov/pubmed/20064271
http://dx.doi.org/10.1186/1471-2334-10-6
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