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利用 CT 放射组学特征和机器学习算法对 COVID-19 进行预后建模:对来自 14339 名患者的多机构数据集的分析。

COVID-19 prognostic modeling using CT radiomic features and machine learning algorithms: Analysis of a multi-institutional dataset of 14,339 patients.

机构信息

Division of Nuclear Medicine and Molecular Imaging, Geneva University Hospital, Geneva, 1211, Switzerland.

Imaging Department, Qom University of Medical Sciences, Qum, Iran.

出版信息

Comput Biol Med. 2022 Jun;145:105467. doi: 10.1016/j.compbiomed.2022.105467. Epub 2022 Mar 29.

DOI:10.1016/j.compbiomed.2022.105467
PMID:35378436
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8964015/
Abstract

BACKGROUND

We aimed to analyze the prognostic power of CT-based radiomics models using data of 14,339 COVID-19 patients.

METHODS

Whole lung segmentations were performed automatically using a deep learning-based model to extract 107 intensity and texture radiomics features. We used four feature selection algorithms and seven classifiers. We evaluated the models using ten different splitting and cross-validation strategies, including non-harmonized and ComBat-harmonized datasets. The sensitivity, specificity, and area under the receiver operating characteristic curve (AUC) were reported.

RESULTS

In the test dataset (4,301) consisting of CT and/or RT-PCR positive cases, AUC, sensitivity, and specificity of 0.83 ± 0.01 (CI95%: 0.81-0.85), 0.81, and 0.72, respectively, were obtained by ANOVA feature selector + Random Forest (RF) classifier. Similar results were achieved in RT-PCR-only positive test sets (3,644). In ComBat harmonized dataset, Relief feature selector + RF classifier resulted in the highest performance of AUC, reaching 0.83 ± 0.01 (CI95%: 0.81-0.85), with a sensitivity and specificity of 0.77 and 0.74, respectively. ComBat harmonization did not depict statistically significant improvement compared to a non-harmonized dataset. In leave-one-center-out, the combination of ANOVA feature selector and RF classifier resulted in the highest performance.

CONCLUSION

Lung CT radiomics features can be used for robust prognostic modeling of COVID-19. The predictive power of the proposed CT radiomics model is more reliable when using a large multicentric heterogeneous dataset, and may be used prospectively in clinical setting to manage COVID-19 patients.

摘要

背景

我们旨在使用来自 14339 例 COVID-19 患者的数据,分析基于 CT 的放射组学模型的预后能力。

方法

使用基于深度学习的模型自动进行全肺分段,以提取 107 个强度和纹理放射组学特征。我们使用了四种特征选择算法和七种分类器。我们使用十种不同的分割和交叉验证策略(包括非协调和 ComBat 协调数据集)评估模型。报告了灵敏度、特异性和接收器操作特征曲线(AUC)下的面积。

结果

在包含 CT 和/或 RT-PCR 阳性病例的测试数据集(4301 例)中,通过方差分析特征选择器+随机森林(RF)分类器,AUC、灵敏度和特异性分别为 0.83±0.01(95%CI:0.81-0.85)、0.81 和 0.72。在仅 RT-PCR 阳性的测试集中也得到了类似的结果(3644 例)。在 ComBat 协调数据集中,Relief 特征选择器+RF 分类器的 AUC 性能最高,达到 0.83±0.01(95%CI:0.81-0.85),灵敏度和特异性分别为 0.77 和 0.74。与非协调数据集相比,ComBat 协调并未显示出统计学上的显著改善。在留一中心外,使用方差分析特征选择器和 RF 分类器的组合可获得最高性能。

结论

肺部 CT 放射组学特征可用于稳健预测 COVID-19 的预后。当使用大型多中心异质数据集时,所提出的 CT 放射组学模型的预测能力更可靠,并且可能在临床环境中前瞻性地用于管理 COVID-19 患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d4/8964015/cf8f2a272000/gr10_lrg.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d4/8964015/0652cb98c529/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d4/8964015/724244131ad8/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d4/8964015/56d829b4c835/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d4/8964015/9f77a849f1de/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d4/8964015/ba272ace0b34/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d4/8964015/b701acb4901b/gr6_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d4/8964015/8789a39f6f18/gr7_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d4/8964015/aa893dc4938d/gr8_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d4/8964015/f76ea1bec9aa/gr9_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d4/8964015/cf8f2a272000/gr10_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d4/8964015/cd915aa2cd0d/ga1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d4/8964015/0652cb98c529/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d4/8964015/724244131ad8/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d4/8964015/56d829b4c835/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d4/8964015/9f77a849f1de/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d4/8964015/ba272ace0b34/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d4/8964015/b701acb4901b/gr6_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d4/8964015/8789a39f6f18/gr7_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d4/8964015/aa893dc4938d/gr8_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d4/8964015/f76ea1bec9aa/gr9_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d4/8964015/cf8f2a272000/gr10_lrg.jpg

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