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CT-Based Intratumoral and Peritumoral Radiomics Nomograms for the Preoperative Prediction of Spread Through Air Spaces in Clinical Stage IA Non-small Cell Lung Cancer.
Wang, Yun; Lyu, Deng; Hu, Lei; Wu, Junhong; Duan, Shaofeng; Zhou, Taohu; Tu, Wenting; Xiao, Yi; Fan, Li; Liu, Shiyuan.
Affiliation
  • Wang Y; Department of Radiology, Second Affiliated Hospital of Navy Medical University, Shanghai, 200003, China.
  • Lyu D; Department of Radiology, Second Affiliated Hospital of Navy Medical University, Shanghai, 200003, China.
  • Hu L; Department of Radiology Medicine, The People's Hospital of Chizhou, Chizhou, Anhui, 247100, China.
  • Wu J; Department of Radiology Medicine, The People's Hospital of Guigang, Guigang, Guangxi Zhuang Autonomous Region, 537100, China.
  • Duan S; GE Healthcare, Precision Health Institution, Shanghai, China.
  • Zhou T; Department of Radiology, Second Affiliated Hospital of Navy Medical University, Shanghai, 200003, China.
  • Tu W; Department of Radiology, Second Affiliated Hospital of Navy Medical University, Shanghai, 200003, China.
  • Xiao Y; Department of Radiology, Second Affiliated Hospital of Navy Medical University, Shanghai, 200003, China.
  • Fan L; Department of Radiology, Second Affiliated Hospital of Navy Medical University, Shanghai, 200003, China. fanli0930@163.com.
  • Liu S; Department of Radiology, Second Affiliated Hospital of Navy Medical University, Shanghai, 200003, China. radiology_cz@163.com.
J Imaging Inform Med ; 37(2): 520-535, 2024 Apr.
Article in En | MEDLINE | ID: mdl-38343212
ABSTRACT
The study aims to investigate the value of intratumoral and peritumoral radiomics and clinical-radiological features for predicting spread through air spaces (STAS) in patients with clinical stage IA non-small cell lung cancer (NSCLC). A total of 336 NSCLC patients from our hospital were randomly divided into the training cohort (n = 236) and the internal validation cohort (n = 100) at a ratio of 73, and 69 patients from the other two external hospitals were collected as the external validation cohort. Univariate and multivariate analyses were used to select clinical-radiological features and construct a clinical model. The GTV, PTV5, PTV10, PTV15, PTV20, GPTV5, GPTV10, GPTV15, and GPTV20 models were constructed based on intratumoral and peritumoral (5 mm, 10 mm, 15 mm, 20 mm) radiomics features. Additionally, the radscore of the optimal radiomics model and clinical-radiological predictors were used to construct a combined model and plot a nomogram. Lastly, the ROC curve and AUC value were used to evaluate the diagnostic performance of the model. Tumor density type (OR = 6.738) and distal ribbon sign (OR = 5.141) were independent risk factors for the occurrence of STAS. The GPTV10 model outperformed the other radiomics models, and its AUC values were 0.887, 0.876, and 0.868 in the three cohorts. The AUC values of the combined model constructed based on GPTV10 radscore and clinical-radiological predictors were 0.901, 0.875, and 0.878. DeLong test results revealed that the combined model was superior to the clinical model in the three cohorts. The nomogram based on GPTV10 radscore and clinical-radiological features exhibited high predictive efficiency for STAS status in NSCLC.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies / Risk_factors_studies Language: En Journal: J Imaging Inform Med Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies / Risk_factors_studies Language: En Journal: J Imaging Inform Med Year: 2024 Document type: Article Affiliation country: Country of publication: