用纠错扩散提升多中心脑肿瘤分割精度
CoMNet: A MedNeXt-CorrDiff Framework for Multi-Site Brain Tumor Segmentation

- 基于MedNeXt与纠错扩散的集成框架,自动修正预测误差
- 在UTSW-Glioma和BraTS-SSA数据集上达到最高Dice分数
- 适合处理多中心扫描差异,提升临床影像分割鲁棒性
从多参数磁共振成像(MRI)中准确分割脑肿瘤对治疗规划、疗效评估和神经肿瘤研究至关重要。然而,由于肿瘤外观和扫描协议在不同患者间存在差异,自动化分割仍是计算机视觉中的难题。此外,增强肿瘤和肿瘤核心等关键区域体积较小,难以实现高精度体素级分割。这些挑战在多中心数据集中尤为突出,因扫描仪硬件和采集参数差异会引入非生物性变异。为此,模型需学习肿瘤特异性特征并抵御站点相关的噪声。本文提出CoMNet,一种融合多折预测与纠错扩散(CorrDiff)后处理的集成框架。采用MedNeXt作为主干网络进行特征学习,纠错扩散模块则对各折预测图的残差误差进行修正,并在概率阈值化前进行集成。该过程通过校正折间残差误差,生成对站点差异不敏感的共识掩码。实验表明,该框架在UTSW-Glioma和BraTS-SSA数据集上优于两个基线模型,验证了纠错扩散与折级概率集成的有效性。
原文摘要 · Abstract (English)
Accurate brain tumor segmentation from multiparametric magnetic resonance imaging (MRI) is critical for treatment planning, response assessment, and neuro-oncology research. However, automated segmentation remains a difficult task in computer vision because of variation in tumor appearance and MRI protocols across patient scans. Moreover, clinically important regions such as enhancing tumor and tumor core are often small relative to the full brain volume, further increasing the difficulty of achieving high voxel-level precision. These challenges are amplified in multi-site datasets, where differences in scanner hardware and acquisition parameters can introduce non-biological variation. To address this, networks must learn tumor-specific features while remaining robust to site-dependent noise. In this paper, we show that an ensemble of multi-fold predictions from a modern 3D convolutional segmentation network with corrective diffusion (CorrDiff) post-processing improves brain tumor segmentation across datasets. We propose CoMNet, an ensembled MedNeXt-CorrDiff framework for accurate multi-site brain tumor segmentation. In this framework, we use MedNeXt as the primary segmentation model for feature learning, while a corrective diffusion block learns to refine the residual errors in the individual prediction maps before probabilistic thresholding. This process reduces the variance across fold predictions by correcting fold-specific residual errors and aggregating them into a consensus mask that is less sensitive to site-dependent imaging variability. Our proposed framework achieved the highest Dice score compared to two baseline models on the UTSW-Glioma and BraTS-SSA datasets. Experimental results support the use of corrective diffusion and fold-level probability ensembling as meaningful additions to existing state-of-the-art models for accurate glioma segmentation on multi-site datasets.
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