CT radiomics facilitates more accurate diagnosis of COVID-19 pneumonia: compared with CO-RADS

Huanhuan Liu(Shanghai Jiao Tong University), Hua Ren(Shanghai Jiao Tong University), Zengbin Wu(Shanghai Jiao Tong University), He Xu(First Affiliated Hospital of Bengbu Medical College), Shuhai Zhang(First Affiliated Hospital of Bengbu Medical College), Jinning Li(Shanghai Jiao Tong University), Liang Hou(Shanghai Jiao Tong University), Runmin Chi(Shanghai Jiao Tong University), Hui Zheng(Shanghai Jiao Tong University), Yanhong Chen(Shanghai Jiao Tong University), Shaofeng Duan(United Imaging Healthcare (China)), Huimin Li(Shanghai Jiao Tong University), Zongyu Xie(First Affiliated Hospital of Bengbu Medical College), Dengbin Wang(Shanghai Jiao Tong University)
Journal of Translational Medicine
January 7, 2021
Cited by 60Open Access
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Abstract

BACKGROUND: Limited data was available for rapid and accurate detection of COVID-19 using CT-based machine learning model. This study aimed to investigate the value of chest CT radiomics for diagnosing COVID-19 pneumonia compared with clinical model and COVID-19 reporting and data system (CO-RADS), and develop an open-source diagnostic tool with the constructed radiomics model. METHODS: This study enrolled 115 laboratory-confirmed COVID-19 and 435 non-COVID-19 pneumonia patients (training dataset, n = 379; validation dataset, n = 131; testing dataset, n = 40). Key radiomics features extracted from chest CT images were selected to build a radiomics signature using least absolute shrinkage and selection operator (LASSO) regression. Clinical and clinico-radiomics combined models were constructed. The combined model was further validated in the viral pneumonia cohort, and compared with performance of two radiologists using CO-RADS. The diagnostic performance was assessed by receiver operating characteristics curve (ROC) analysis, calibration curve, and decision curve analysis (DCA). RESULTS: Eight radiomics features and 5 clinical variables were selected to construct the combined radiomics model, which outperformed the clinical model in diagnosing COVID-19 pneumonia with an area under the ROC (AUC) of 0.98 and good calibration in the validation cohort. The combined model also performed better in distinguishing COVID-19 from other viral pneumonia with an AUC of 0.93 compared with 0.75 (P = 0.03) for clinical model, and 0.69 (P = 0.008) or 0.82 (P = 0.15) for two trained radiologists using CO-RADS. The sensitivity and specificity of the combined model can be achieved to 0.85 and 0.90. The DCA confirmed the clinical utility of the combined model. An easy-to-use open-source diagnostic tool was developed using the combined model. CONCLUSIONS: The combined radiomics model outperformed clinical model and CO-RADS for diagnosing COVID-19 pneumonia, which can facilitate more rapid and accurate detection.


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