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The effects of time valuation in cancer optimal therapies: a study of chronic myeloid leukemia

BACKGROUND: The mathematical design of optimal therapies to fight cancer is an important research field in today’s Biomathematics and Biomedicine given its relevance to formulate patient-specific treatments. Until now, however, cancer optimal therapies have considered that malignancy exclusively dep...

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Autores principales: Gutiérrez-Diez, Pedro José, López-Marcos, Miguel Ángel, Martínez-Rodríguez, Julia, Russo, Jose
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6540446/
https://www.ncbi.nlm.nih.gov/pubmed/31138288
http://dx.doi.org/10.1186/s12976-019-0106-4
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author Gutiérrez-Diez, Pedro José
López-Marcos, Miguel Ángel
Martínez-Rodríguez, Julia
Russo, Jose
author_facet Gutiérrez-Diez, Pedro José
López-Marcos, Miguel Ángel
Martínez-Rodríguez, Julia
Russo, Jose
author_sort Gutiérrez-Diez, Pedro José
collection PubMed
description BACKGROUND: The mathematical design of optimal therapies to fight cancer is an important research field in today’s Biomathematics and Biomedicine given its relevance to formulate patient-specific treatments. Until now, however, cancer optimal therapies have considered that malignancy exclusively depends on the drug concentration and the number of cancer cells, ignoring that the faster the cancer grows the worse the cancer is, and that early drug doses are more prejudicial. Here, we analyze how optimal therapies are affected when the time evolution of treated cancer is envisaged as an additional element determining malignancy, analyzing in detail the implications for imatinib-treated Chronic Myeloid Leukemia. METHODS: Taking as reference a mathematical model describing Chronic Myeloid Leukemia dynamics, we design an optimal therapy problem by modifying the usual malignancy objective function, unaware of any temporal dimension of cancer malignance. In particular, we introduce a time valuation factor capturing the increase of malignancy associated to the quick development of the disease and the persistent negative effects of initial drug doses. After assigning values to the parameters involved, we solve and simulate the model with and without the new time valuation factor, comparing the results for the drug doses and the evolution of the disease. RESULTS: Our computational simulations unequivocally show that the consideration of a time valuation factor capturing the higher malignancy associated with early growth of cancer and drug administration allows more efficient therapies to be designed. More specifically, when this time valuation factor is incorporated into the objective function, the optimal drug doses are lower, and do not involve medically relevant increases in the number of cancer cells or in the disease duration. CONCLUSIONS: In the light of our simulations and as biomedical evidence strongly suggests, the existence of a time valuation factor affecting malignancy in treated cancer cannot be ignored when designing cancer optimal therapies. Indeed, the consideration of a time valuation factor modulating malignancy results in significant gains of efficiency in the optimal therapy with relevant implications from the biomedical perspective, specially when designing patient-specific treatments.
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spelling pubmed-65404462019-06-03 The effects of time valuation in cancer optimal therapies: a study of chronic myeloid leukemia Gutiérrez-Diez, Pedro José López-Marcos, Miguel Ángel Martínez-Rodríguez, Julia Russo, Jose Theor Biol Med Model Research BACKGROUND: The mathematical design of optimal therapies to fight cancer is an important research field in today’s Biomathematics and Biomedicine given its relevance to formulate patient-specific treatments. Until now, however, cancer optimal therapies have considered that malignancy exclusively depends on the drug concentration and the number of cancer cells, ignoring that the faster the cancer grows the worse the cancer is, and that early drug doses are more prejudicial. Here, we analyze how optimal therapies are affected when the time evolution of treated cancer is envisaged as an additional element determining malignancy, analyzing in detail the implications for imatinib-treated Chronic Myeloid Leukemia. METHODS: Taking as reference a mathematical model describing Chronic Myeloid Leukemia dynamics, we design an optimal therapy problem by modifying the usual malignancy objective function, unaware of any temporal dimension of cancer malignance. In particular, we introduce a time valuation factor capturing the increase of malignancy associated to the quick development of the disease and the persistent negative effects of initial drug doses. After assigning values to the parameters involved, we solve and simulate the model with and without the new time valuation factor, comparing the results for the drug doses and the evolution of the disease. RESULTS: Our computational simulations unequivocally show that the consideration of a time valuation factor capturing the higher malignancy associated with early growth of cancer and drug administration allows more efficient therapies to be designed. More specifically, when this time valuation factor is incorporated into the objective function, the optimal drug doses are lower, and do not involve medically relevant increases in the number of cancer cells or in the disease duration. CONCLUSIONS: In the light of our simulations and as biomedical evidence strongly suggests, the existence of a time valuation factor affecting malignancy in treated cancer cannot be ignored when designing cancer optimal therapies. Indeed, the consideration of a time valuation factor modulating malignancy results in significant gains of efficiency in the optimal therapy with relevant implications from the biomedical perspective, specially when designing patient-specific treatments. BioMed Central 2019-05-28 /pmc/articles/PMC6540446/ /pubmed/31138288 http://dx.doi.org/10.1186/s12976-019-0106-4 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License(http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Gutiérrez-Diez, Pedro José
López-Marcos, Miguel Ángel
Martínez-Rodríguez, Julia
Russo, Jose
The effects of time valuation in cancer optimal therapies: a study of chronic myeloid leukemia
title The effects of time valuation in cancer optimal therapies: a study of chronic myeloid leukemia
title_full The effects of time valuation in cancer optimal therapies: a study of chronic myeloid leukemia
title_fullStr The effects of time valuation in cancer optimal therapies: a study of chronic myeloid leukemia
title_full_unstemmed The effects of time valuation in cancer optimal therapies: a study of chronic myeloid leukemia
title_short The effects of time valuation in cancer optimal therapies: a study of chronic myeloid leukemia
title_sort effects of time valuation in cancer optimal therapies: a study of chronic myeloid leukemia
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6540446/
https://www.ncbi.nlm.nih.gov/pubmed/31138288
http://dx.doi.org/10.1186/s12976-019-0106-4
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