A radiomics nomogram analysis based on CT images and clinical features for preoperative Lauren classification in gastric cancer

Purpose To develop a combined radiomics nomogram based on computed tomography (CT) images and clinical features to preoperatively distinguish Lauren’s diffuse-type gastric cancer (GC) from intestinal-type GC. Methods Ninety-five patients with Lauren’s intestinal or diffuse-type GC confirmed by posto...

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Veröffentlicht in:Japanese journal of radiology 2023-04, Vol.41 (4), p.401-408
Hauptverfasser: Nie, Tingting, Liu, Dan, Ai, Shuangquan, He, Yaoyao, Yang, Miao, Chen, Jun, Yuan, Zilong, Liu, Yulin
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Sprache:eng
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Zusammenfassung:Purpose To develop a combined radiomics nomogram based on computed tomography (CT) images and clinical features to preoperatively distinguish Lauren’s diffuse-type gastric cancer (GC) from intestinal-type GC. Methods Ninety-five patients with Lauren’s intestinal or diffuse-type GC confirmed by postoperative pathology had their preoperative clinical information and dynamic contrast CT images retrospectively analyzed and were subdivided into training and test groups in a 7:3 ratio. To select the optimal features and construct the radiomic signatures, we extracted, filtered, and minimized the radiomic features from arterial phase (AP) and venous phase (VP) CT images. We constructed four models (clinical model, AP radiomics model, VP radiomics model, and radiomics-clinical model) to assess and compare their predictive performance between the intestinal- and diffuse-type GC. Receiver-operating characteristic (ROC) curve, area under the ROC curve (AUC), and the DeLong test were used for assessment and comparison. In this study, radiomic nomograms integrating combined radiomic signatures and clinical characteristics were developed. Results Compared to the AP radiomics model, the VP radiomics model had better performance, with an AUC of 0.832 (95% confidence interval [CI], 0.735, 0.929) in the training cohort and 0.760 (95% CI 0.580, 0.940) in the test cohort. Among the combined models that assessed Lauren’s type GC, the model including age and VP radiomics showed the best performance, with an AUC of 0.849 (95% CI 0.758, 0.940) in the training cohort and 0.793 (95% CI 0.629, 0.957) in the test cohort. Conclusions Nomogram incorporating radiomic signatures and clinical features effectively differentiated Lauren’s diffuse-type from intestinal-type GC.
ISSN:1867-1071
1867-108X
DOI:10.1007/s11604-022-01360-4