Rios Piedra Edgar A, Taira Ricky K, El-Saden Suzie, Ellingson Benjamin M, Bui Alex A T, Hsu William
Department of Radiological Sciences at the University of California, Los Angeles, CA. Department of Bioengineering at the University of California, Los Angeles, CA. Medical Imaging Informatics (MII) at the University of California, Los Angeles, CA.
Department of Radiological Sciences at the University of California, Los Angeles, CA. Department of Bioengineering at the University of California, Los Angeles, CA. Medical Imaging Informatics (MII) at the University of California, Los Angeles, CA. Department of Radiology, Veterans Administration Greater Los Angeles Healthcare, Los Angeles, CA.
IEEE EMBS Int Conf Biomed Health Inform. 2016 Feb;2016:380-383. doi: 10.1109/BHI.2016.7455914. Epub 2016 Apr 21.
Brain tumor analysis is moving towards volumetric assessment of magnetic resonance imaging (MRI), providing a more precise description of disease progression to better inform clinical decision-making and treatment planning. While a multitude of segmentation approaches exist, inherent variability in the results of these algorithms may incorrectly indicate changes in tumor volume. In this work, we present a systematic approach to characterize variability in tumor boundaries that utilizes equivalence tests as a means to determine whether a tumor volume has significantly changed over time. To demonstrate these concepts, 32 MRI studies from 8 patients were segmented using four different approaches (statistical classifier, region-based, edge-based, knowledge-based) to generate different regions of interest representing tumor extent. We showed that across all studies, the average Dice coefficient for the superset of the different methods was 0.754 (95% confidence interval 0.701-0.808) when compared to a reference standard. We illustrate how variability obtained by different segmentations can be used to identify significant changes in tumor volume between sequential time points. Our study demonstrates that variability is an inherent part of interpreting tumor segmentation results and should be considered as part of the interpretation process.
脑肿瘤分析正朝着磁共振成像(MRI)的容积评估发展,以更精确地描述疾病进展情况,从而为临床决策和治疗规划提供更充分的信息。虽然存在多种分割方法,但这些算法结果中固有的变异性可能会错误地指示肿瘤体积的变化。在这项工作中,我们提出了一种系统的方法来表征肿瘤边界的变异性,该方法利用等效性检验来确定肿瘤体积是否随时间发生了显著变化。为了证明这些概念,我们使用四种不同的方法(统计分类器、基于区域、基于边缘、基于知识)对8名患者的32项MRI研究进行了分割,以生成代表肿瘤范围的不同感兴趣区域。我们发现,与参考标准相比,在所有研究中,不同方法的超集的平均骰子系数为0.754(95%置信区间0.701 - 0.808)。我们说明了如何利用不同分割获得的变异性来识别连续时间点之间肿瘤体积的显著变化。我们的研究表明,变异性是解释肿瘤分割结果的一个固有部分,应作为解释过程的一部分加以考虑。