评估脑肿瘤分割的可变性以提高体积准确性和变化特征。

Edgar A Rios Piedra, Ricky K Taira, Suzie El-Saden, Benjamin M Ellingson, Alex A T Bui, William Hsu
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引用次数: 7

摘要

脑肿瘤分析正朝着磁共振成像(MRI)的体积评估方向发展,提供更精确的疾病进展描述,以更好地为临床决策和治疗计划提供信息。虽然存在多种分割方法,但这些算法结果的固有可变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可变性,该方法利用等效试验作为确定肿瘤体积是否随时间发生显着变化的手段。为了证明这些概念,使用四种不同的方法(统计分类器,基于区域的,基于边缘的,基于知识的)对8名患者的32份MRI研究进行分割,以生成代表肿瘤范围的不同感兴趣区域。我们发现,在所有研究中,与参考标准相比,不同方法的超集的平均Dice系数为0.754(95%置信区间0.701-0.808)。我们说明了通过不同分割获得的可变性如何用于识别连续时间点之间肿瘤体积的显着变化。我们的研究表明,可变性是解释肿瘤分割结果的固有部分,应被视为解释过程的一部分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Assessing Variability in Brain Tumor Segmentation to Improve Volumetric Accuracy and Characterization of Change.

Assessing Variability in Brain Tumor Segmentation to Improve Volumetric Accuracy and Characterization of Change.

Assessing Variability in Brain Tumor Segmentation to Improve Volumetric Accuracy and Characterization of Change.

Assessing Variability in Brain Tumor Segmentation to Improve Volumetric Accuracy and Characterization of Change.

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.

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