Dual-energy CT-based radiomics in predicting EGFR mutation status non-invasively in lung adenocarcinoma

Jing Wen Ma, Xu Jiang, Yan Mei Wang, Jiu Ming Jiang, Lei Miao, Lin Lin Qi, Jia Xing Zhang, Xin Wen, Jian Wei Li, Meng Li, Li Zhang

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

Objectives: Patients with epidermal growth factor receptor (EGFR) mutations in lung adenocarcinoma (LUAD) can benefit from individualized targeted therapy. This study aims to develop, compare, analyse prediction models based on dual-energy spectral computed tomography (DESCT) and CT-based radiomic features to non-invasively predict EGFR mutation status in LUAD. Materials and methods: Patients with LUAD (n = 175), including 111 patients with and 64 patients without EGFR mutations, were enrolled in the current study. All patients were randomly divided into a training dataset (122 cases) and validation dataset (53 cases) at a ratio of 7:3. After extracting CT-based radiomic, DESCT and clinical features, we built seven prediction models and a nomogram of the best prediction. Receiver operating characteristic (ROC) curves and the mean area under the curve (AUC) values were used for comparisons among the models to obtain the best prediction model for predicting EGFR mutations. Results: The best distinguishing ability is the combined model incorporating radiomic, DESCT and clinical features for predicting the EGFR mutation status with an AUC of 0.86 (95 % CI: 0.79–0.92) in the training group and an AUC value of 0.83 (95 % CI: 0.73, 0.96) in the validation group. Conclusions: Our study provides a predictive nomogram non-invasively with a combination of CT-based radiomic, DESCT and clinical features, which can provide image-based biological information for targeted therapy of LUAD with EGFR mutations.

Original languageEnglish
Article numbere24372
JournalHeliyon
Volume10
Issue number2
DOIs
StatePublished - 30 Jan 2024
Externally publishedYes

Keywords

  • CT-based radiomics
  • Dual-energy spectral CT
  • EGFR mutation
  • Lung adenocarcinoma
  • Nomogram

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