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Efficient Hilbert transform-based alternative to Tofts physiological models for representing MRI dynamic contrast-enhanced images in computer-aided diagnosis of prostate cancer

机译:基于Hilbert变换的高效Tofts生理模型替代品,用于在前列腺癌的计算机辅助诊断中代表MRI动态对比增强的图像

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In computer-aided diagnosis (CAD) systems for prostate cancer, dynamic contrast enhanced (DCE) magnetic resonance imaging is useful for distinguishing cancerous and benign tissue. The Tofts physiological model is a commonly used representation of the DCE image data, but the parameters require extensive computation. Hence, we developed an alternative representation based on the Hilbert transform of the DCE images. The time maximum of the Hilbert transform, a binary metric of early enhancement, and a pre-DCE value was assigned to each voxel and appended to a standard feature set derived from T2-weighted images and apparent diffusion coefficient maps. A cohort of 40 patients was used for training the classifier, and 20 patients were used for testing. The AUC was calculated by pooling the voxel-wise prediction values and comparing with the ground truth. The resulting AUC of 0.92 (95% CI [0.87 0.97]) is not significantly different from an AUC calculated using Tofts physiological models of 0.92 (95% CI [0.87 0.97]), as validated by a Wilcoxon signed rank test on each patient's AUC (p = 0.19). The time required for calculation and feature extraction is 11.39 seconds (95% CI [10.95 11.82]) per patient using the Hilbert-based feature set, two orders of magnitude faster than the 1319 seconds (95% CI [1233 1404]) required for the Tofts parameter-based feature set (p<0.001). Hence, the features proposed herein appear useful for CAD systems integrated into clinical workflows where efficiency is important.
机译:在前列腺癌的计算机辅助诊断(CAD)系统中,动态对比增强(DCE)磁共振成像可用于区分癌变组织和良性组织。 Tofts生理模型是DCE图像数据的常用表示形式,但是参数需要大量计算。因此,我们基于DCE图像的希尔伯特变换开发了一种替代表示形式。将Hilbert变换的最大时间,早期增强的二进制度量和DCE之前的值分配给每个体素,并将其附加到从T2加权图像和视在扩散系数图得出的标准特征集。一组40名患者用于训练分类器,而20名患者用于测试。通过合并体素方向的预测值并与地面真实情况进行比较来计算AUC。最终的AUC为0.92(95%CI [0.87 0.97])与使用Tofts的0.92生理模型计算的AUC(95%CI [0.87 0.97])并无显着差异,这一点已通过针对每个患者AUC的Wilcoxon符号秩检验进行了验证(p = 0.19)。使用基于希尔伯特的特征集,每位患者计算和特征提取所需的时间为11.39秒(95%CI [10.95 11.82]),比计算所需的1319秒(95%CI [1233 1404])快两个数量级。基于Tofts参数的功能集(p <0.001)。因此,本文提出的特征对于集成到效率很重要的临床工作流程中的CAD系统似乎很有用。

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