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Multiple-reader, multiple-case ROC analysis for determining the limit of calcification detection in tomosynthesis

机译:多读器,多案ROC分析,用于确定钙化检测限制

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We have conducted virtual clinical trials (VCTs) of digital breast tomosynthesis (DBT) to evaluate the parameters that affect detectability of breast lesions. The OpenVCT framework was used to simulate the breast anatomy and imaging systems. We generated 36 anthropomorphic breast phantoms (700 ml volume, 6.33 cm compressed thickness), varying the number of simulated tissue compartments and their shape. We inserted 42 calcifications into each phantom with variable sizes of 1-3 voxels. DBT projections of phantoms with and without lesions were synthesized assuming a clinical acquisition geometry. We varied the detector element size (140 μm and 70 μm), the source motion (continuous and stepand-shoot), and the reconstructed voxel size (100 μm and 70 μm). The reconstructed images were cropped in the plane where the calcifications are located, with regions of interest (ROIs) centered on the lesion position. We also simulated virtual readers to evaluate the calcification detectability using multiple-reader, multiple-case method, using Barco's Medical Virtual Image Chain (MeVIC) software. Human readers were simulated using channelized Hotelling observers with 15 Laguerre-Gauss channels. We used spreads of 22 and 31, and ROIs of 150×150 and 214×214 pixels for images reconstructed with pixel size of 100 μm and 70 μm, respectively. Reconstructed voxels of 70μm provided better overall calcification detection, especially for small calcifications. For one-voxel polycubes, the difference in AUC using five readers was 6.5% (0.713 and 0.667). The impact of calcification detection from most to least significant is: reconstruction voxel size, source motion, and detector element size, especially for small calcifications.
机译:我们已经进行了数字乳房Tomosynthesis(DBT)的虚拟临床试验(VCT),以评估影响乳腺病变可检测性的参数。 OpenVCT框架用于模拟乳房解剖和成像系统。我们生成36个拟方针乳膜(700mL体积,6.33cm压缩厚度),改变模拟组织隔室的数量及其形状。我们将42个钙化插入每个幻像,具有1-3个体素的可变大小。假设临床采集几何形状,合成了具有和不具有病变的幽灵的DBT投影。我们改变了检测器元件尺寸(140μm和70μm),源运动(连续和步骤和拍摄),以及重建的体素尺寸(100μm和70μm)。在钙化位于钙化的平面中裁剪重建的图像,其中感兴趣的区域(ROI)以病变位置为中心。我们还模拟虚拟读者使用多读器,多种情况法使用Barco的医疗虚拟图像链(MEVIC)软件来评估钙化可检测性。使用带15个Laguerre-Gauss渠道的通道化热身观察员模拟人类读者。我们使用了22和31的差点,以及150×150和214×214像素的ROI,用于图像分别以100μm和70μm的像素尺寸重建。重建的70μm的体素提供了更好的整体钙化检测,特别是对于小钙化。对于单voxel polycubes,使用五个读者的AUC差异为6.5%(0.713和0.667)。钙化检测对大多数至最低重大的影响是:重建体素大小,源运动和检测器元件尺寸,特别是对于小钙化。

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