Paper ID: 2411.00594

Deep learning-based auto-contouring of organs/structures-at-risk for pediatric upper abdominal radiotherapy

Mianyong Ding, Matteo Maspero, Annemieke S Littooij, Martine van Grotel, Raquel Davila Fajardo, Max M van Noesel, Marry M van den Heuvel-Eibrink, Geert O Janssens

Purposes: This study aimed to develop a computed tomography (CT)-based multi-organ segmentation model for delineating organs-at-risk (OARs) in pediatric upper abdominal tumors and evaluate its robustness across multiple datasets. Materials and methods: In-house postoperative CTs from pediatric patients with renal tumors and neuroblastoma (n=189) and a public dataset (n=189) with CTs covering thoracoabdominal regions were used. Seventeen OARs were delineated: nine by clinicians (Type 1) and eight using TotalSegmentator (Type 2). Auto-segmentation models were trained using in-house (ModelPMC-UMCU) and a combined dataset of public data (Model-Combined). Performance was assessed with Dice Similarity Coefficient (DSC), 95% Hausdorff Distance (HD95), and mean surface distance (MSD). Two clinicians rated clinical acceptability on a 5-point Likert scale across 15 patient contours. Model robustness was evaluated against sex, age, intravenous contrast, and tumor type. Results: Model-PMC-UMCU achieved mean DSC values above 0.95 for five of nine OARs, while spleen and heart ranged between 0.90 and 0.95. The stomach-bowel and pancreas exhibited DSC values below 0.90. Model-Combined demonstrated improved robustness across both datasets. Clinical evaluation revealed good usability, with both clinicians rating six of nine Type 1 OARs above four and six of eight Type 2 OARs above three. Significant performance 2 differences were only found across age groups in both datasets, specifically in the left lung and pancreas. The 0-2 age group showed the lowest performance. Conclusion: A multi-organ segmentation model was developed, showcasing enhanced robustness when trained on combined datasets. This model is suitable for various OARs and can be applied to multiple datasets in clinical settings.

Submitted: Nov 1, 2024