Roniotis Alexandros, Sakkalis Vangelis, Karatzanis Ioannis, Zervakis Michalis E, Marias Kostas
Institute of Computer Science, Foundation for Research and Technology, Heraklion, Greece.
IEEE Trans Inf Technol Biomed. 2012 May;16(3):299-307. doi: 10.1109/TITB.2012.2185704. Epub 2012 Jan 23.
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.
神经胶质瘤是最具侵袭性的脑肿瘤类型之一。在过去二十年中,已经开发了几种数学模型,用于模拟控制神经胶质瘤发展的机制。最常见的模型使用扩散反应方程(DRE)来模拟肿瘤细胞浓度的时空变化。然而,尽管有相关应用,但在研究三维扩散模型的数学解和实现细节以及对算法结果进行定性分析方面,工作仍很少。本文提出了一个使用不同数值格式求解DRE的完整数学框架。该框架考虑了最新模型的所有特征,如脑组织异质性、各向异性肿瘤细胞迁移、化疗和切除建模。所提出的不同数值格式已根据逼近DRE精确解的程度进行了评估。已经在真实数据集和有已知解代数表达式的测试案例上进行了实验。因此,可以计算不同模型的准确性。