Image-based personalization of computational models for predicting response of high-grade glioma to chemoradiation
Abstract High-grade gliomas are an aggressive and invasive malignancy which are susceptible to treatment resistance due to heterogeneity in intratumoral properties such as cell proliferation and density and perfusion. Non-invasive imaging approaches can measure these properties, which can then be us...
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2021
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oai:doaj.org-article:55eb86d0b3a0467cb8f80d1460fdead22021-12-02T13:39:47ZImage-based personalization of computational models for predicting response of high-grade glioma to chemoradiation10.1038/s41598-021-87887-42045-2322https://doaj.org/article/55eb86d0b3a0467cb8f80d1460fdead22021-04-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-87887-4https://doaj.org/toc/2045-2322Abstract High-grade gliomas are an aggressive and invasive malignancy which are susceptible to treatment resistance due to heterogeneity in intratumoral properties such as cell proliferation and density and perfusion. Non-invasive imaging approaches can measure these properties, which can then be used to calibrate patient-specific mathematical models of tumor growth and response. We employed multiparametric magnetic resonance imaging (MRI) to identify tumor extent (via contrast-enhanced T 1 -weighted, and T 2 -FLAIR) and capture intratumoral heterogeneity in cell density (via diffusion-weighted imaging) to calibrate a family of mathematical models of chemoradiation response in nine patients with unresected or partially resected disease. The calibrated model parameters were used to forecast spatially-mapped individual tumor response at future imaging visits. We then employed the Akaike information criteria to select the most parsimonious member from the family, a novel two-species model describing the enhancing and non-enhancing components of the tumor. Using this model, we achieved low error in predictions of the enhancing volume (median: − 2.5%, interquartile range: 10.0%) and a strong correlation in total cell count (Kendall correlation coefficient 0.79) at 3-months post-treatment. These preliminary results demonstrate the plausibility of using multiparametric MRI data to inform spatially-informative, biologically-based predictive models of tumor response in the setting of clinical high-grade gliomas.David A. HormuthKarine A. Al FeghaliAndrew M. ElliottThomas E. YankeelovCaroline ChungNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-14 (2021) |
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Medicine R Science Q David A. Hormuth Karine A. Al Feghali Andrew M. Elliott Thomas E. Yankeelov Caroline Chung Image-based personalization of computational models for predicting response of high-grade glioma to chemoradiation |
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Abstract High-grade gliomas are an aggressive and invasive malignancy which are susceptible to treatment resistance due to heterogeneity in intratumoral properties such as cell proliferation and density and perfusion. Non-invasive imaging approaches can measure these properties, which can then be used to calibrate patient-specific mathematical models of tumor growth and response. We employed multiparametric magnetic resonance imaging (MRI) to identify tumor extent (via contrast-enhanced T 1 -weighted, and T 2 -FLAIR) and capture intratumoral heterogeneity in cell density (via diffusion-weighted imaging) to calibrate a family of mathematical models of chemoradiation response in nine patients with unresected or partially resected disease. The calibrated model parameters were used to forecast spatially-mapped individual tumor response at future imaging visits. We then employed the Akaike information criteria to select the most parsimonious member from the family, a novel two-species model describing the enhancing and non-enhancing components of the tumor. Using this model, we achieved low error in predictions of the enhancing volume (median: − 2.5%, interquartile range: 10.0%) and a strong correlation in total cell count (Kendall correlation coefficient 0.79) at 3-months post-treatment. These preliminary results demonstrate the plausibility of using multiparametric MRI data to inform spatially-informative, biologically-based predictive models of tumor response in the setting of clinical high-grade gliomas. |
format |
article |
author |
David A. Hormuth Karine A. Al Feghali Andrew M. Elliott Thomas E. Yankeelov Caroline Chung |
author_facet |
David A. Hormuth Karine A. Al Feghali Andrew M. Elliott Thomas E. Yankeelov Caroline Chung |
author_sort |
David A. Hormuth |
title |
Image-based personalization of computational models for predicting response of high-grade glioma to chemoradiation |
title_short |
Image-based personalization of computational models for predicting response of high-grade glioma to chemoradiation |
title_full |
Image-based personalization of computational models for predicting response of high-grade glioma to chemoradiation |
title_fullStr |
Image-based personalization of computational models for predicting response of high-grade glioma to chemoradiation |
title_full_unstemmed |
Image-based personalization of computational models for predicting response of high-grade glioma to chemoradiation |
title_sort |
image-based personalization of computational models for predicting response of high-grade glioma to chemoradiation |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/55eb86d0b3a0467cb8f80d1460fdead2 |
work_keys_str_mv |
AT davidahormuth imagebasedpersonalizationofcomputationalmodelsforpredictingresponseofhighgradegliomatochemoradiation AT karineaalfeghali imagebasedpersonalizationofcomputationalmodelsforpredictingresponseofhighgradegliomatochemoradiation AT andrewmelliott imagebasedpersonalizationofcomputationalmodelsforpredictingresponseofhighgradegliomatochemoradiation AT thomaseyankeelov imagebasedpersonalizationofcomputationalmodelsforpredictingresponseofhighgradegliomatochemoradiation AT carolinechung imagebasedpersonalizationofcomputationalmodelsforpredictingresponseofhighgradegliomatochemoradiation |
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1718392615423967232 |