Transfer learning-based PET/CT three-dimensional convolutional neural network fusion of image and clinical information for prediction of EGFR mutation in lung adenocarcinoma

被引:4
|
作者
Shao, Xiaonan [1 ,2 ]
Ge, Xinyu [1 ,2 ]
Gao, Jianxiong [1 ,2 ]
Niu, Rong [1 ,2 ]
Shi, Yunmei [1 ,2 ]
Shao, Xiaoliang [1 ,2 ]
Jiang, Zhenxing [3 ]
Li, Renyuan [4 ,5 ]
Wang, Yuetao [1 ,2 ]
机构
[1] Soochow Univ, Affiliated Hosp 3, Dept Nucl Med, Changzhou 213003, Peoples R China
[2] Soochow Univ, Inst Clin Translat Nucl Med & Mol Imaging, Changzhou 213003, Peoples R China
[3] Soochow Univ, Affiliated Hosp 3, Dept Radiol, Changzhou 213003, Peoples R China
[4] Zhejiang Univ, Sch Med, Interdisciplinary Inst Neurosci & Technol, Hangzhou 310009, Peoples R China
[5] Zhejiang Univ, Sir Run Run Shaw Hosp, Sch Med, Hangzhou, Peoples R China
关键词
Lung adenocarcinoma; Positron emission tomography/computed tomography; Deep learning; radiomics; Epidermal growth factor receptor; ESMO CONSENSUS CONFERENCE; CONVENTIONAL CT; CANCER; DIAGNOSIS; FEATURES;
D O I
10.1186/s12880-024-01232-5
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Background To introduce a three-dimensional convolutional neural network (3D CNN) leveraging transfer learning for fusing PET/CT images and clinical data to predict EGFR mutation status in lung adenocarcinoma (LADC). Methods Retrospective data from 516 LADC patients, encompassing preoperative PET/CT images, clinical information, and EGFR mutation status, were divided into training (n = 404) and test sets (n = 112). Several deep learning models were developed utilizing transfer learning, involving CT-only and PET-only models. A dual-stream model fusing PET and CT and a three-stream transfer learning model (TS_TL) integrating clinical data were also developed. Image preprocessing includes semi-automatic segmentation, resampling, and image cropping. Considering the impact of class imbalance, the performance of the model was evaluated using ROC curves and AUC values. Results TS_TL model demonstrated promising performance in predicting the EGFR mutation status, with an AUC of 0.883 (95%CI = 0.849-0.917) in the training set and 0.730 (95%CI = 0.629-0.830) in the independent test set. Particularly in advanced LADC, the model achieved an AUC of 0.871 (95%CI = 0.823-0.919) in the training set and 0.760 (95%CI = 0.638-0.881) in the test set. The model identified distinct activation areas in solid or subsolid lesions associated with wild and mutant types. Additionally, the patterns captured by the model were significantly altered by effective tyrosine kinase inhibitors treatment, leading to notable changes in predicted mutation probabilities. Conclusion PET/CT deep learning model can act as a tool for predicting EGFR mutation in LADC. Additionally, it offers clinicians insights for treatment decisions through evaluations both before and after treatment.
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页数:13
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