Evolution of resistance to anti-cancer therapy during general dosing schedules Journal Article


Authors: Foo, J.; Michor, F.
Article Title: Evolution of resistance to anti-cancer therapy during general dosing schedules
Abstract: Anti-cancer drugs targeted to specific oncogenic pathways have shown promising therapeutic results in the past few years; however, drug resistance remains an important obstacle for these therapies. Resistance to these drugs can emerge due to a variety of reasons including genetic or epigenetic changes which alter the binding site of the drug target, cellular metabolism or export mechanisms. Obtaining a better understanding of the evolution of resistant populations during therapy may enable the design of more effective therapeutic regimens which prevent or delay progression of disease due to resistance. In this paper, we use stochastic mathematical models to study the evolutionary dynamics of resistance under time-varying dosing schedules and pharmacokinetic effects. The populations of sensitive and resistant cells are modeled as multi-type non-homogeneous birth-death processes in which the drug concentration affects the birth and death rates of both the sensitive and resistant cell populations in continuous time. This flexible model allows us to consider the effects of generalized treatment strategies as well as detailed pharmacokinetic phenomena such as drug elimination and accumulation over multiple doses. We develop estimates for the probability of developing resistance and moments of the size of the resistant cell population. With these estimates, we optimize treatment schedules over a subspace of tolerated schedules to minimize the risk of disease progression due to resistance as well as locate ideal schedules for controlling the population size of resistant clones in situations where resistance is inevitable. Our methodology can be used to describe dynamics of resistance arising due to a single (epi)genetic alteration in any tumor type. © 2009 Elsevier Ltd.
Keywords: cancer chemotherapy; controlled study; area under the curve; cancer growth; antineoplastic agents; antineoplastic agent; neoplasms; metabolism; drug administration schedule; evolution; drug resistance; drug resistance, neoplasm; cancer mortality; cancer resistance; mathematical model; models, theoretical; cancer genetics; drug accumulation; probability; epigenetics; disease progression; cancer cell; binding site; tumor; drug dose regimen; cell metabolism; dose-response relationship; resistance; drug elimination; targeted cancer therapy; antibiotics; stochastic models; stochasticity
Journal Title: Journal of Theoretical Biology
Volume: 263
Issue: 2
ISSN: 0022-5193
Publisher: Elsevier Inc.  
Date Published: 2010-03-21
Start Page: 179
End Page: 188
Language: English
DOI: 10.1016/j.jtbi.2009.11.022
PUBMED: 20004211
PROVIDER: scopus
PMCID: PMC2826560
DOI/URL:
Notes: --- - "Cited By (since 1996): 2" - "Export Date: 20 April 2011" - "CODEN: JTBIA" - "Source: Scopus"
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  1. Franziska Michor
    23 Michor
  2. Jasmine Yen-Teng Foo
    6 Foo