基于深度学习的儿童上腹部放疗危及器官/结构自动勾画
Deep learning-based auto-contouring of organs/structures-at-risk for pediatric upper abdominal radiotherapy
AI总结:
本研究针对儿童上腹部放疗危及器官勾画需求,开发基于CT的多器官分割模型,通过内部与公开组合数据集训练提升鲁棒性,经量化指标与临床评估验证了良好性能与可用性。
摘要:
目的:本研究旨在开发一种基于计算机断层扫描(CT)的多器官分割模型,用于勾画儿童上腹部肿瘤的危及器官(OARs),并评估其在多个数据集上的鲁棒性。材料与方法:研究使用了来自肾肿瘤和神经母细胞瘤患儿的内部术后CT数据(n=189),以及一个涵盖胸腹部区域CT的公开数据集(n=189)。共勾画了17个危及器官:其中9个由临床医生勾画(1类),8个使用TotalSegmentator勾画(2类)。分别使用内部数据集训练了自动分割模型Model-PMC-UMCU,使用公开数据的组合数据集训练了Model-Combined。采用戴斯相似系数(DSC)、95%豪斯多夫距离(HD95)和平均表面距离(MSD)评估模型性能。两名临床医生采用5点李克特量表对15例患者的勾画结果进行临床可接受性评分。模型鲁棒性则从性别、年龄、静脉造影剂和肿瘤类型四个维度进行评估。结果:Model-PMC-UMCU在9个1类危及器官中有5个的平均DSC值高于0.95,脾脏和心脏的DSC值在0.90至0.95之间,胃肠和胰腺的DSC值低于0.90。Model-Combined在两个数据集上均表现出更强的鲁棒性。临床评估显示模型可用性良好,两名临床医生对9个1类危及器官中的6个评分高于4分,对8个2类危及器官中的6个评分高于3分。仅在两个数据集的年龄组间发现显著的性能差异,具体体现在左肺和胰腺上,其中0-2岁年龄组的性能最低。结论:本研究开发了一种多器官分割模型,经组合数据集训练后鲁棒性得到提升。该模型适用于多种危及器官的勾画,可应用于临床场景中的多个数据集。
英文摘要:
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.
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