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Initial Condition Assessment for Reaction-Diffusion Glioma Growth Models: A Translational MRI-Histology (In)Validation Study

Reaction-diffusion models have been proposed for decades to capture the growth of gliomas. Nevertheless, these models require an initial condition: the tumor cell density distribution over the whole brain at diagnosis time. Several works have proposed to relate this distribution to abnormalities vis...

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Autores principales: Martens, Corentin, Lebrun, Laetitia, Decaestecker, Christine, Vandamme, Thomas, Van Eycke, Yves-Rémi, Rovai, Antonin, Metens, Thierry, Debeir, Olivier, Goldman, Serge, Salmon, Isabelle, Van Simaeys, Gaetan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8628987/
https://www.ncbi.nlm.nih.gov/pubmed/34842805
http://dx.doi.org/10.3390/tomography7040055
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author Martens, Corentin
Lebrun, Laetitia
Decaestecker, Christine
Vandamme, Thomas
Van Eycke, Yves-Rémi
Rovai, Antonin
Metens, Thierry
Debeir, Olivier
Goldman, Serge
Salmon, Isabelle
Van Simaeys, Gaetan
author_facet Martens, Corentin
Lebrun, Laetitia
Decaestecker, Christine
Vandamme, Thomas
Van Eycke, Yves-Rémi
Rovai, Antonin
Metens, Thierry
Debeir, Olivier
Goldman, Serge
Salmon, Isabelle
Van Simaeys, Gaetan
author_sort Martens, Corentin
collection PubMed
description Reaction-diffusion models have been proposed for decades to capture the growth of gliomas. Nevertheless, these models require an initial condition: the tumor cell density distribution over the whole brain at diagnosis time. Several works have proposed to relate this distribution to abnormalities visible on magnetic resonance imaging (MRI). In this work, we verify these hypotheses by stereotactic histological analysis of a non-operated brain with glioblastoma using a 3D-printed slicer. Cell density maps are computed from histological slides using a deep learning approach. The density maps are then registered to a postmortem MR image and related to an MR-derived geodesic distance map to the tumor core. The relation between the edema outlines visible on T2-FLAIR MRI and the distance to the core is also investigated. Our results suggest that (i) the previously proposed exponential decrease of the tumor cell density with the distance to the core is reasonable but (ii) the edema outlines would not correspond to a cell density iso-contour and (iii) the suggested tumor cell density at these outlines is likely overestimated. These findings highlight the limitations of conventional MRI to derive glioma cell density maps and the need for other initialization methods for reaction-diffusion models to be used in clinical practice.
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spelling pubmed-86289872021-11-30 Initial Condition Assessment for Reaction-Diffusion Glioma Growth Models: A Translational MRI-Histology (In)Validation Study Martens, Corentin Lebrun, Laetitia Decaestecker, Christine Vandamme, Thomas Van Eycke, Yves-Rémi Rovai, Antonin Metens, Thierry Debeir, Olivier Goldman, Serge Salmon, Isabelle Van Simaeys, Gaetan Tomography Article Reaction-diffusion models have been proposed for decades to capture the growth of gliomas. Nevertheless, these models require an initial condition: the tumor cell density distribution over the whole brain at diagnosis time. Several works have proposed to relate this distribution to abnormalities visible on magnetic resonance imaging (MRI). In this work, we verify these hypotheses by stereotactic histological analysis of a non-operated brain with glioblastoma using a 3D-printed slicer. Cell density maps are computed from histological slides using a deep learning approach. The density maps are then registered to a postmortem MR image and related to an MR-derived geodesic distance map to the tumor core. The relation between the edema outlines visible on T2-FLAIR MRI and the distance to the core is also investigated. Our results suggest that (i) the previously proposed exponential decrease of the tumor cell density with the distance to the core is reasonable but (ii) the edema outlines would not correspond to a cell density iso-contour and (iii) the suggested tumor cell density at these outlines is likely overestimated. These findings highlight the limitations of conventional MRI to derive glioma cell density maps and the need for other initialization methods for reaction-diffusion models to be used in clinical practice. MDPI 2021-10-29 /pmc/articles/PMC8628987/ /pubmed/34842805 http://dx.doi.org/10.3390/tomography7040055 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Martens, Corentin
Lebrun, Laetitia
Decaestecker, Christine
Vandamme, Thomas
Van Eycke, Yves-Rémi
Rovai, Antonin
Metens, Thierry
Debeir, Olivier
Goldman, Serge
Salmon, Isabelle
Van Simaeys, Gaetan
Initial Condition Assessment for Reaction-Diffusion Glioma Growth Models: A Translational MRI-Histology (In)Validation Study
title Initial Condition Assessment for Reaction-Diffusion Glioma Growth Models: A Translational MRI-Histology (In)Validation Study
title_full Initial Condition Assessment for Reaction-Diffusion Glioma Growth Models: A Translational MRI-Histology (In)Validation Study
title_fullStr Initial Condition Assessment for Reaction-Diffusion Glioma Growth Models: A Translational MRI-Histology (In)Validation Study
title_full_unstemmed Initial Condition Assessment for Reaction-Diffusion Glioma Growth Models: A Translational MRI-Histology (In)Validation Study
title_short Initial Condition Assessment for Reaction-Diffusion Glioma Growth Models: A Translational MRI-Histology (In)Validation Study
title_sort initial condition assessment for reaction-diffusion glioma growth models: a translational mri-histology (in)validation study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8628987/
https://www.ncbi.nlm.nih.gov/pubmed/34842805
http://dx.doi.org/10.3390/tomography7040055
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