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Application of computed tomography-based radiomics in differential diagnosis of adenocarcinoma and squamous cell carcinoma at the esophagogastric junction

Authors :
Ke-Pu Du
Wen-Peng Huang
Si-Yun Liu
Yun-Jin Chen
Li-Ming Li
Xiao-Nan Liu
Yi-Jing Han
Yue Zhou
Chen-Chen Liu
Jian-Bo Gao
Source :
World journal of gastroenterology. 28(31)
Publication Year :
2022

Abstract

The biological behavior of carcinoma of the esophagogastric junction (CEGJ) is different from that of gastric or esophageal cancer. Differentiating squamous cell carcinoma of the esophagogastric junction (SCCEG) from adenocarcinoma of the esophagogastric junction (AEG) can indicate Siewert stage and whether the surgical route for patients with CEGJ is transthoracic or transabdominal, as well as aid in determining the extent of lymph node dissection. With the development of neoadjuvant therapy, preoperative determination of pathological type can help in the selection of neoadjuvant radiotherapy and chemotherapy regimens.To establish and evaluate computed tomography (CT)-based multiscale and multiphase radiomics models to distinguish SCCEG and AEG preoperatively.We retrospectively analyzed the preoperative contrasted-enhanced CT imaging data of single-center patients with pathologically confirmed SCCEG (The 2D-venous model (5 features, AUC: 0.849) performed better than 2D-arterial (5 features, AUC: 0.808). The 2D-arterial-venous combined model could further enhance the performance (AUC: 0.869). The 3D-venous model (7 features, AUC: 0.877) performed better than 3D-arterial (10 features, AUC: 0.876). And the 3D-arterial-venous combined model (AUC: 0.904) outperformed other single-phase-based models. The venous model showed a positive improvement compared with the arterial model (NRI0, IDI0), and the 3D-venous and combined models showed a significant positive improvement compared with the 2D-venous and combined models (The combined arterial-venous CT radiomics model based on 3D segmentation can improve the performance in differentiating EGJ squamous cell carcinoma from adenocarcinoma.

Details

ISSN :
22192840
Volume :
28
Issue :
31
Database :
OpenAIRE
Journal :
World journal of gastroenterology
Accession number :
edsair.doi.dedup.....551f1965b5ca52c6b3a170a95959c18b