In-Depth Analysis and Evaluation of Diffusive Glioma Models

Glioma is one of the most aggressive types of brain tumor. Several mathematical models have been developed during the past two decades, toward simulating the mechanisms that govern the development of glioma. The most common models use the diffusion-reaction equation (DRE) for simulating the spatiote...

Full description

Saved in:
Bibliographic Details
Published inIEEE transactions on information technology in biomedicine Vol. 16; no. 3; pp. 299 - 307
Main Authors Roniotis, A., Sakkalis, V., Karatzanis, I., Zervakis, M. E., Marias, K.
Format Journal Article
LanguageEnglish
Published United States IEEE 01.05.2012
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Glioma is one of the most aggressive types of brain tumor. Several mathematical models have been developed during the past two decades, toward simulating the mechanisms that govern the development of glioma. The most common models use the diffusion-reaction equation (DRE) for simulating the spatiotemporal variation of tumor cell concentration. Nevertheless, despite the applications presented, there has been little work on studying the details of the mathematical solution and implementation of the 3-D diffusion model and presenting a qualitative analysis of the algorithmic results. This paper presents a complete mathematical framework on the solution of the DRE using different numerical schemes. This framework takes into account all characteristics of the latest models, such as brain tissue heterogeneity, anisotropic tumor cell migration, chemotherapy, and resection modeling. The different numerical schemes presented have been evaluated based upon the degree to which the DRE exact solution is approximated. Experiments have been conducted both on real datasets and a test case for which there is a known algebraic expression of the solution. Thus, it is possible to calculate the accuracy of the different models.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1089-7771
1558-0032
DOI:10.1109/TITB.2012.2185704