通过引入解剖先验提升肾上腺嗜铬细胞瘤分割精度
A Study of Anatomical Priors for Deep Learning-Based Segmentation of Pheochromocytoma in Abdominal CT
- 用邻近器官解剖结构构建多类别标注策略
- 肾脏+主动脉先验使分割准确率提升25.84%
- 对不同基因亚型患者均表现稳定,适合临床应用
在腹部CT中精准分割嗜铬细胞瘤(PCC)对评估肿瘤负荷、预后判断和治疗规划至关重要,也可能帮助推断遗传分型,减少昂贵检测依赖。本研究系统评估解剖先验对深度学习分割性能的影响,采用nnU-Net框架,在91名患者的105例增强CT扫描数据上测试11种标注策略,提出基于肝、脾、肾、主动脉、肾上腺、胰腺等邻近器官的新型多类别先验方案。与以往研究中的体部先验相比,肿瘤+肾+主动脉(TKA)策略在70-30训练测试划分下显著优于肿瘤+体部(TB):Dice系数(p=0.0097)、归一化表面距离(p=0.0110)、F1分数提升25.84%(IoU阈值0.5)。五折交叉验证中,TKA在0.1至0.5的IoU阈值下持续领先。该模型肿瘤负荷量化相关性达R²=0.968,且在所有遗传亚型中表现良好,证明结合解剖上下文能显著提升分割精度,为临床评估与长期随访提供有力工具。
原文摘要 · Abstract (English)
Accurate segmentation of pheochromocytoma (PCC) in abdominal CT scans is essential for tumor burden estimation, prognosis, and treatment planning. It may also help infer genetic clusters, reducing reliance on expensive testing. This study systematically evaluates anatomical priors to identify configurations that improve deep learning-based PCC segmentation. We employed the nnU-Net framework to evaluate eleven annotation strategies for accurate 3D segmentation of pheochromocytoma, introducing a set of novel multi-class schemes based on organ-specific anatomical priors. These priors were derived from adjacent organs commonly surrounding adrenal tumors (e.g., liver, spleen, kidney, aorta, adrenal gland, and pancreas), and were compared against a broad body-region prior used in previous work. The framework was trained and tested on 105 contrast-enhanced CT scans from 91 patients at the NIH Clinical Center. Performance was measured using Dice Similarity Coefficient (DSC), Normalized Surface Distance (NSD), and instance-wise F1 score. Among all strategies, the Tumor + Kidney + Aorta (TKA) annotation achieved the highest segmentation accuracy, significantly outperforming the previously used Tumor + Body (TB) annotation across DSC (p = 0.0097), NSD (p = 0.0110), and F1 score (25.84% improvement at an IoU threshold of 0.5), measured on a 70-30 train-test split. The TKA model also showed superior tumor burden quantification (R^2 = 0.968) and strong segmentation across all genetic subtypes. In five-fold cross-validation, TKA consistently outperformed TB across IoU thresholds (0.1 to 0.5), reinforcing its robustness and generalizability. These findings highlight the value of incorporating relevant anatomical context into deep learning models to achieve precise PCC segmentation, offering a valuable tool to support clinical assessment and longitudinal disease monitoring in PCC patients.
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