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Radiomics in differential diagnosis of pancreatic tumors
Riccardo De Robertis, Beatrice Mascarin, Eda Bardhi, Flavio Spoto, Nicoḷ Cardobi, Mirko D'Onofrio
Eur J Radiol Open. 2025 May 6:14:100651. doi: 10.1016/j.ejro.2025.100651. eCollection 2025 Jun.Abstract
The aim of this study was to assess whether radiomics could predict histotype of pancreatic ductal adenocarcinomas (PDAC) and pancreatic neuroendocrine tumors (PNET). Contrast-enhanced CT scans of 193 patients were retrospectively reviewed, encompassing 97 PDACs and 96 PNETs. Additionally, anamnestic data and laboratory data were evaluated. A total of 107 features were extracted for both the arterial and venous phases. ROC curves were constructed for the parameters with the highest AUC, considering two groups: one including all lesions and the other including only lesions smaller than 5 cm. The following feature differences were found to be statistically significant (p < 0.05). Without considering lesion size: for the arterial phase, 16 first-order and 38 s-order features; for the venous phase, 10 first-order and 20 s-order features. When considering lesion size: for the arterial phase, 16 first-order and 52 s-order features; for the venous phase, 11 first-order and 36 s-order features. The radiomics features with the highest AUC values included ART_firstorder_RootMeanSquared (AUC = 0.896, p < 0.01) in the arterial phase and VEN_firstorder_Median (AUC = 0.737, p < 0.05) in the venous phase for all lesions, and ART_firstorder_RootMeanSquared (AUC = 0.859, p < 0.01) and VEN_firstorder_Median (AUC = 0.713, p < 0.05) for lesions smaller than 5 cm. Texture analysis of pancreatic pathology has shown good predictability in defining the PNET histotype. This analysis potentially offering a non-invasive, imaging-based method to accurately differentiate between pancreatic tumor types. Such advancements could lead to more precise and personalized treatment planning, ultimately optimizing the use of medical resources.