Development and Validation of a Deep Learning Radiomics Model to Predict High-Risk Pathologic Pulmonary Nodules Using Preoperative Computed Tomography

医学 队列 无线电技术 接收机工作特性 置信区间 逻辑回归 曲线下面积 放射科 核医学 内科学
作者
Guanchao Ye,Guangyao Wu,Kuo Li,Chi Zhang,Yuzhou Zhuang,Hong Liu,Enmin Song,Yu Qi,Yiying Li,Fan Yang,Yongde Liao
出处
期刊:Academic Radiology [Elsevier BV]
卷期号:31 (4): 1686-1697 被引量:9
标识
DOI:10.1016/j.acra.2023.08.040
摘要

Rationale and Objectives To accurately identify the high-risk pathological factors of pulmonary nodules, our study constructed a model combined with clinical features, radiomics features, and deep transfer learning features to predict high-risk pathological pulmonary nodules. Materials and Methods The study cohort consisted of 469 cases of lung adenocarcinoma patients, divided into a training cohort (n = 400) and an external validation cohort (n = 69). We obtained computed tomography (CT) semantic features and clinical characteristics, as well as extracted radiomics and deep transfer learning (DTL) features from the CT images. Selected features were used for constructing prediction models using the logistic regression (LR) algorithm. The performance of the models was evaluated through metrics including the area under the receiver operating characteristic curve (AUC), sensitivity, specificity, calibration curve, and decision curve analysis. Results The clinical model achieved an AUC of 0.774 (95% CI: 0.728–0.821) in the training cohort and 0.762 (95% confidence interval [CI]: 0.650–0.873) in the external validation cohort. The radiomics model demonstrated an AUC of 0.847 (95% CI: 0.810–0.884) in the training cohort and 0.800 (95% CI: 0.693–0.907) in the external validation cohort. The radiomics-DTL (Rad-DTL) model showed an AUC of 0.871 (95% CI: 0.838–0.905) in the training cohort and 0.806 (95% CI: 0.698–0.914) in the external validation cohort. The proposed combined model yielded AUC values of 0.872 and 0.814 in the training and external validation cohorts, respectively. The combined model demonstrated superiority over both the clinical model and the Rad-DTL model. There were no statistically significant differences observed in the comparison between the combined model incorporating clinical features and the Rad-DTL model. Decision curve analysis (DCA) indicated that the models provided a net benefit in predicting high-risk pathologic pulmonary nodules. Conclusion Rad-DTL signature is a potential biomarker for predicting high-risk pathologic pulmonary nodules using preoperative CT, determining the appropriate surgical strategy, and guiding the extent of resection. To accurately identify the high-risk pathological factors of pulmonary nodules, our study constructed a model combined with clinical features, radiomics features, and deep transfer learning features to predict high-risk pathological pulmonary nodules. The study cohort consisted of 469 cases of lung adenocarcinoma patients, divided into a training cohort (n = 400) and an external validation cohort (n = 69). We obtained computed tomography (CT) semantic features and clinical characteristics, as well as extracted radiomics and deep transfer learning (DTL) features from the CT images. Selected features were used for constructing prediction models using the logistic regression (LR) algorithm. The performance of the models was evaluated through metrics including the area under the receiver operating characteristic curve (AUC), sensitivity, specificity, calibration curve, and decision curve analysis. The clinical model achieved an AUC of 0.774 (95% CI: 0.728–0.821) in the training cohort and 0.762 (95% confidence interval [CI]: 0.650–0.873) in the external validation cohort. The radiomics model demonstrated an AUC of 0.847 (95% CI: 0.810–0.884) in the training cohort and 0.800 (95% CI: 0.693–0.907) in the external validation cohort. The radiomics-DTL (Rad-DTL) model showed an AUC of 0.871 (95% CI: 0.838–0.905) in the training cohort and 0.806 (95% CI: 0.698–0.914) in the external validation cohort. The proposed combined model yielded AUC values of 0.872 and 0.814 in the training and external validation cohorts, respectively. The combined model demonstrated superiority over both the clinical model and the Rad-DTL model. There were no statistically significant differences observed in the comparison between the combined model incorporating clinical features and the Rad-DTL model. Decision curve analysis (DCA) indicated that the models provided a net benefit in predicting high-risk pathologic pulmonary nodules. Rad-DTL signature is a potential biomarker for predicting high-risk pathologic pulmonary nodules using preoperative CT, determining the appropriate surgical strategy, and guiding the extent of resection.
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