计算机辅助诊断模型在CT图像中检测多器官肿块病变的外部和内部验证。

Lian-Yan Xu, Ke Yan, Le Lu, Wei-Hong Zhang, Xu Chen, Xiao-Fei Huo, Jing-Jing Lu
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引用次数: 1

摘要

目的研制一种在室内实验中表现良好的通用病变检测器(ULDor)。该研究旨在通过外部和内部验证来评估其在临床环境中的表现及其推广能力。ULDor系统由卷积神经网络(CNN)组成,该网络对来自DeepLesion数据集和其他5个公共器官特异性数据集的约12K CT研究的约80K病变注释进行了训练。在验证过程中,测试集包括两部分:外部验证数据集由来自某综合性医院的164组非对比胸部和上腹部CT扫描组成,内部验证数据集由来自国家肺筛查试验(NLST)的187组低剂量螺旋CT扫描组成。我们在两个测试集上运行模型以输出病变检测。三名委员会认证的放射科医生阅读CT扫描并验证ULDor的检测结果。我们采用阳性预测值(positive predictive value, PPV)和敏感性评价该模型在CT图像上显示的肺外器官占位性病变的检测效果,包括肝、肾、胰腺、肾上腺、脾脏、食道、甲状腺、淋巴结、体壁、胸椎等。结果经外部验证,该模型的病灶水平PPV和灵敏度分别为57.9%和67.0%。该模型平均每组检测出2.1个结果,其中0.9个为假阳性。ULDor对肝脏病变的检测效果较好,PPV为78.9%,敏感性为92.7%,其次是肾脏,PPV为70.0%,敏感性为58.3%。在NLST测试集的内部验证中,ULDor获得了75.3%的PPV和52.0%的灵敏度,尽管软组织对图像的噪声水平相对较高。结论基于外部真实世界数据的ULDor性能测试表明其在某些器官病变的多用途检测中具有较高的有效性。通过进一步的优化和迭代升级,ULDor可能非常适合外部数据的广泛应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
External and Internal Validation of a Computer Assisted Diagnostic Model for Detecting Multi-Organ Mass Lesions in CT images.

Objective We developed a universal lesion detector (ULDor) which showed good performance in in-lab experiments. The study aims to evaluate the performance and its ability to generalize in clinical setting via both external and internal validation. Methods The ULDor system consists of a convolutional neural network (CNN) trained on around 80K lesion annotations from about 12K CT studies in the DeepLesion dataset and 5 other public organ-specific datasets. During the validation process, the test sets include two parts: the external validation dataset which was comprised of 164 sets of non-contrasted chest and upper abdomen CT scans from a comprehensive hospital, and the internal validation dataset which was comprised of 187 sets of low-dose helical CT scans from the National Lung Screening Trial (NLST). We ran the model on the two test sets to output lesion detection. Three board-certified radiologists read the CT scans and verified the detection results of ULDor. We used positive predictive value (PPV) and sensitivity to evaluate the performance of the model in detecting space-occupying lesions at all extra-pulmonary organs visualized on CT images, including liver, kidney, pancreas, adrenal, spleen, esophagus, thyroid, lymph nodes, body wall, thoracic spine, etc. Results In the external validation, the lesion-level PPV and sensitivity of the model were 57.9% and 67.0%, respectively. On average, the model detected 2.1 findings per set, and among them, 0.9 were false positives. ULDor worked well for detecting liver lesions, with a PPV of 78.9% and a sensitivity of 92.7%, followed by kidney, with a PPV of 70.0% and a sensitivity of 58.3%. In internal validation with NLST test set, ULDor obtained a PPV of 75.3% and a sensitivity of 52.0% despite the relatively high noise level of soft tissue on images. Conclusions The performance tests of ULDor with the external real-world data have shown its high effectiveness in multiple-purposed detection for lesions in certain organs. With further optimisation and iterative upgrades, ULDor may be well suited for extensive application to external data.

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