TY - JOUR
T1 - Tracking glioblastoma progression after initial resection with minimal reaction-diffusion models
AU - Harris, Duane C.
AU - Mignucci-Jiménez, Giancarlo
AU - Xu, Yuan
AU - Eikenberry, Steffen E.
AU - Quarles, C. Chad
AU - Preul, Mark C.
AU - Kuang, Yang
AU - Kostelich, Eric J.
N1 - Funding Information:
This work was funded by the Arizona Biomedical Research Commission under grant number ADH516-162514. Additional support was provided from the Newsome Chair in Neurosurgery Research held by Mark C. Preul; the National Institutes of Health under award number 5R01GM131405-02 and by the National Science Foundation under grant DMS-1757663 to Yang Kuang; and by funds from the School of Mathematical and Statistical Sciences at Arizona State University.
Publisher Copyright:
© 2022 the Author(s).
PY - 2022
Y1 - 2022
N2 - We describe a preliminary effort to model the growth and progression of glioblastoma multiforme, an aggressive form of primary brain cancer, in patients undergoing treatment for recurrence of tumor following initial surgery and chemoradiation. Two reaction-diffusion models are used: the Fisher-Kolmogorov equation and a 2-population model, developed by the authors, that divides the tumor into actively proliferating and quiescent (or necrotic) cells. The models are simulated on 3- dimensional brain geometries derived from magnetic resonance imaging (MRI) scans provided by the Barrow Neurological Institute. The study consists of 17 clinical time intervals across 10 patients that have been followed in detail, each of whom shows significant progression of tumor over a period of 1 to 3 months on sequential follow up scans. A Taguchi sampling design is implemented to estimate the variability of the predicted tumors to using 144 different choices of model parameters. In 9 cases, model parameters can be identified such that the simulated tumor, using both models, contains at least 40 percent of the volume of the observed tumor. We discuss some potential improvements that can be made to the parameterizations of the models and their initialization.
AB - We describe a preliminary effort to model the growth and progression of glioblastoma multiforme, an aggressive form of primary brain cancer, in patients undergoing treatment for recurrence of tumor following initial surgery and chemoradiation. Two reaction-diffusion models are used: the Fisher-Kolmogorov equation and a 2-population model, developed by the authors, that divides the tumor into actively proliferating and quiescent (or necrotic) cells. The models are simulated on 3- dimensional brain geometries derived from magnetic resonance imaging (MRI) scans provided by the Barrow Neurological Institute. The study consists of 17 clinical time intervals across 10 patients that have been followed in detail, each of whom shows significant progression of tumor over a period of 1 to 3 months on sequential follow up scans. A Taguchi sampling design is implemented to estimate the variability of the predicted tumors to using 144 different choices of model parameters. In 9 cases, model parameters can be identified such that the simulated tumor, using both models, contains at least 40 percent of the volume of the observed tumor. We discuss some potential improvements that can be made to the parameterizations of the models and their initialization.
KW - Fisher-Kolmogorov model
KW - ensemble prediction
KW - glioblastoma multiforme
KW - magnetic resonance imaging
KW - parameter estimation
KW - reaction-diffusion equations
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U2 - 10.3934/mbe.2022256
DO - 10.3934/mbe.2022256
M3 - Article
C2 - 35603364
AN - SCOPUS:85127937334
SN - 1547-1063
VL - 19
SP - 5446
EP - 5481
JO - Mathematical Biosciences and Engineering
JF - Mathematical Biosciences and Engineering
IS - 6
ER -