Evidence map›Paper›PMID 31138288›Full record

ArticleTheoretical biology & medical modelling2019

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

Pedro José Gutiérrez-Diez, Miguel Ángel López-Marcos, Julia Martínez-Rodríguez, Jose Russo

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Article in Theoretical biology & medical modelling, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 39% of its field
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed, 2 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors at 2 institutions in 2 countries.

Pedro José Gutiérrez-DiezDepartment of Economic Theory and IMUVA, Faculty of Economics, Avda. Valle Esgueva 6, University of Valladolid, Valladolid, 47011, Spain. pedrojos@fae.uva.es.ORCID 0000-0003-4816-615X
Miguel Ángel López-MarcosDepartment of Applied Mathematics and IMUVA, Faculty of Science, University of Valladolid, Paseo de Belén 7, Valladolid, 47011, Spain.
Julia Martínez-RodríguezDepartment of Applied Economics and IMUVA, Faculty of Economics, University of Valladolid, Avda. Valle Esgueva 6, Valladolid, 47011, Spain.
Jose RussoDirector of the Breast Cancer Research Laboratory, Fox Chase Cancer Center, 333 Cottman Avenue, Philadelphia, 19111-2497, PA, USA.
Universidad de Valladolid · ESFox Chase Cancer Center · US

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Dietmar J Kappes · 1985 to 2026
$138.8M
NCI NIH HHS P30 CA006927
6 · The paper itself

Abstract

backgroundThe 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.

methodsTaking 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.

resultsOur 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.

conclusionsIn 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.

Indexed as

CalibrationCell CommunicationHumansLeukemia, Myelogenous, Chronic, BCR-ABL PositiveModels, BiologicalTime FactorsChronic myeloid leukemiaHematopoiesisImatinib therapyOptimal control problemSystem of difference equationsTime valuation factor

Identifiers

PMID31138288
PMCPMC6540446
OpenAlexW2947310095

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.