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[Preprint]. 2025 May 30:rs.3.rs-6622868.
doi: 10.21203/rs.3.rs-6622868/v1.

Multi-center evaluation of radiomics and deep learning to stratify malignancy risk of IPMNs

Affiliations

Multi-center evaluation of radiomics and deep learning to stratify malignancy risk of IPMNs

Andrea M Bejar et al. Res Sq. .

Abstract

Distinguishing high-risk intraductal papillary mucinous neoplasms (IPMNs), pancreatic cysts requiring surgery, from low-risk lesions remains a clinical challenge, often resulting in unnecessary procedures due to limited specificity of current methods. While radiomics and deep learning (DL) have been explored for pancreatic cancer, cyst-level malignancy risk stratification of IPMNs remains untapped. We conducted a multi-institutional study (seven centers, 359 T2W MRI images) to assess the feasibility of AI for predicting IPMN dysplasia grade using cyst-level image features. We developed and compared 2D and 3D radiomics-only, deep learning (DL)-only, and radiomics-DL fusion models, using expert radiologist scoring as a baseline reference. Model performance was evaluated using held-out test data. The radiomics-DL fusion model showed the highest discriminatory ability on the test set (AUC 0.692), outperforming the radiomics-only model (AUC 0.665). Expert accuracy varied widely (37.4%-66.7%). The fusion model integrating deep learning and radiomics features from routine T2W MRI (AUC: 0.692) demonstrates potential for objective, cyst-level risk stratification of IPMNs in a multi-center cohort, outperforming both radiomics-only models and expert radiologists. While performance requires improvement for standalone clinical use, this approach offers a scalable, non-invasive method to potentially improve diagnostic accuracy and reduce unnecessary surgical interventions.

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Conflict of interest statement

Authors declare no conflict of interest except the following ones: Dr. Ulas Bagci acknowledges: Ther-AI LLC. Dr. Pallavi Tiwari is an equity holder in LivAI Inc. and serves as a scientific consultant for Johnson & Johnson. Dr. Rajesh N. Keswani acknowledges: Boston Scientific - consultant; Olympus - consultant; Medtronic - consultant and research support. Dr. Michael B. Wallace acknowledges Boston Scientific, ClearNote Health, Cosmo Pharmaceuticals, Endostart, Endiatix, Fujifilm, Medtronic, Surgical Automations, Ohelio Ltd, Venn Bioscience, Virgo Inc., Surgical Automation, and Microtek. Dr. Marco J. Bruno acknowledges: Boston Scientific - consultant, support for industry and investigator-initiated studies; Cook Medical - consultant, support for industry and investigator-initiated studies; Pentax Medical - consultant, support for investigator-initiated studies; Mylan - support for investigator initiated studies; AMBU - consultant, support for investigator initiated studies; ChiRoStim - support for investigator-initiated studies.Additional Declarations: No competing interests reported.

Figures

Figure 1
Figure 1
UMAP of quality indicators (projected into x and y axes from 21 quality indicators) per center using different normalization methods. Centers: Mayo Clinic Florida (MCF), Mayo Clinic Arizona (MCA), Northwestern Memorial Hospitals (NMH), New York University (NYU), Allegheny Health Network (AHN), Istanbul University (IU) Hospital, and Erasmus Medical Center (EMC).
Figure 2
Figure 2
Representative T2-weighted (T2W) images and reference segmentations of high-grade and low-grade IPMNs. The first row shows T2W MRI images, and the second row shows reference segmentations of high-grade and low-grade, main-duct (MD)-IPMN and branch-duct (BD)-IPMN cases.
Figure 3
Figure 3
Receiver operating characteristic curve of 2D and 3D radiomics predictions distinguishing between Low and High-Risk groups in the testing set.
Figure 4
Figure 4
Low vs High Risk classification comparison in cross-validation set’s mean (%) AUC, accuracy, and F1 for 2D and 3D radiomic analyses. Means are written above the error bars, and error bars show standard deviation.
Figure 5
Figure 5
Low vs High Risk classification comparison of mean (%) AUC, accuracy, and F1 between cross-validation and testing trials for 2D and 3D radiomic analyses. Values above each bar represent the mean value. Error bars show standard deviation.
Figure 6
Figure 6
Diagram of patient selection, data set curation, and radiomics and deep learning (DL) pipelines. (A) 746 patients were selected and received MRI imaging from seven centers between three countries; images were then preprocessed and manually segmented. (B) 2D and 3D radiomic features were extracted and classified using a random forest algorithm. (C) A DL-only analysis was conducted, then we developed a radiomics-DL fusion algorithm.
Figure 7
Figure 7
Flowchart of the subject selection and classification.

References

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