Asclepios Research Project-INRIA, 2004 Route des Lucioles, 06902, Sophia Antipolis, France.
Med Image Anal. 2010 Apr;14(2):111-25. doi: 10.1016/j.media.2009.11.005. Epub 2009 Dec 3.
Radiotherapy for brain glioma treatment relies on magnetic resonance (MR) and computed tomography (CT) images. These images provide information on the spatial extent of the tumor, but can only visualize parts of the tumor where cancerous cells are dense enough, masking the low density infiltration. In radiotherapy, a 2 m constant margin around the tumor is taken to account for this uncertainty. This approach however, does not consider the growth dynamics of gliomas, particularly the differential motility of tumor cells in the white and in the gray matter. In this article, we propose a novel method for estimating the full extent of the tumor infiltration starting from its visible mass in the patients' MR images. This estimation problem is a time independent problem where we do not have information about the temporal evolution of the pathology nor its initial conditions. Based on the reaction-diffusion models widely used in the literature, we derive a method to solve this extrapolation problem. Later, we use this formulation to tailor new tumor specific variable irradiation margins. We perform geometrical comparisons between the conventional constant and the proposed variable margins through determining the amount of targeted tumor cells and healthy tissue in the case of synthetic tumors. Results of these experiments suggest that the variable margin could be more effective at targeting cancerous cells and preserving healthy tissue.
脑胶质瘤的放射治疗依赖于磁共振(MR)和计算机断层扫描(CT)图像。这些图像提供了肿瘤空间范围的信息,但只能显示出癌细胞密集的肿瘤的部分区域,掩盖了低密度浸润。在放射治疗中,肿瘤周围取 2 厘米的恒定边界来考虑这种不确定性。然而,这种方法没有考虑到胶质瘤的生长动态,特别是肿瘤细胞在白质和灰质中的不同运动能力。在本文中,我们提出了一种从患者的 MR 图像中可见肿瘤质量开始估计肿瘤浸润的完整范围的新方法。这个估计问题是一个与时间无关的问题,我们没有关于病理学的时间演化或其初始条件的信息。基于文献中广泛使用的反应扩散模型,我们推导出一种解决这种外推问题的方法。之后,我们使用这个公式来定制新的肿瘤特异性可变照射边界。我们通过确定合成肿瘤中靶向肿瘤细胞和健康组织的数量,对常规常数和建议的可变边界进行几何比较。这些实验的结果表明,可变边界在靶向癌细胞和保护健康组织方面可能更有效。