Predicting Gene Comutation of EGFR and TP53 by Radiomics and Deep Learning in Patients With Lung Adenocarcinomas
- Xiao-Yan Wang 1, Shao-Hong Wu 1, Jiao Ren 1, Yan Zeng 2, Li-Li Guo 1
- Xiao-Yan Wang 1, Shao-Hong Wu 1, Jiao Ren 1
- 1Department of Radiology, the Affiliated Huaian No. 1 People's Hospital of Nanjing Medical University, Huaian.
- 2Department of Research Center, Shanghai United Imaging Intelligence Co., Ltd., Shanghai, China.
- 0Department of Radiology, the Affiliated Huaian No. 1 People's Hospital of Nanjing Medical University, Huaian.
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View abstract on PubMed
Summary
This summary is machine-generated.This study developed radiomics and deep learning models to predict EGFR and TP53 mutations in lung adenocarcinoma, aiding in identifying patients for targeted therapy and predicting prognoses.
Area Of Science
- Oncology
- Radiology
- Bioinformatics
Background
- Lung adenocarcinoma (LUAD) treatment is increasingly personalized.
- Identifying patients with specific genetic mutations like EGFR and TP53 is crucial for effective targeted therapy.
- Accurate prediction of these mutations can guide treatment decisions and improve patient outcomes.
Purpose Of The Study
- To construct and evaluate progressive binary classification models using radiomics and deep learning.
- To predict the presence of epidermal growth factor receptor (EGFR) and TP53 mutations in LUAD patients.
- To assess model performance in identifying patients suitable for TKI-targeted therapy and those with poor prognoses.
Main Methods
- Retrospective analysis of 267 LUAD patients with genetic testing and noncontrast chest CT.
- Feature extraction from regions of interest (ROIs) and construction of clinical, radiomics, deep learning (DL), and ensemble models.
- Model performance evaluated using Area Under the Curve (AUC), sensitivity, specificity, accuracy, precision, and F1 score.
Main Results
- The DL-rad-clin model achieved the highest AUC (0.783) for predicting EGFR status.
- For TP53 status in EGFR-mutated patients, the rad-clin model showed the highest AUC (0.811).
- Ensemble models combining clinical, radiomics, and DL features demonstrated superior predictive capabilities.
Conclusions
- Radiomics and deep learning-based classification models offer a valuable tool for predicting EGFR and TP53 mutations in LUAD.
- These models can serve as a reference to complement clinical identification of TKI responders and patients with poor prognoses.
- The findings support the integration of advanced imaging analysis in precision oncology for lung cancer.
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