NSB-H2GAN:“负样本”增强的分层异构图注意网络,用于整张幻灯片图像的可解释分类

Meiyan Liang;Shupeng Zhang;Xikai Wang;Bo Li;Muhammad Hamza Javed;Xiaojun Jia;Lin Wang
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引用次数: 0

摘要

由于不同幻灯片和单个幻灯片的特征范围不同,千兆像素全幻灯片图像(WSI)预测和兴趣区域定位面临相当大的挑战。目前的大多数方法依赖于弱监督学习,使用同构图在幻灯片中建立上下文感知的相关性,往往忽略了病理图像中固有的丰富多样性的异构信息。受决定性点过程(DPP)的负采样策略和病理切片的分层结构的启发,我们引入了负样本增强的分层异构图注意网络(NSB-H2GAN)。该模型解决了经典图形卷积网络(GCNs)在应用于病理切片时通常遇到的过度平滑问题。通过在多个尺度上合并“负样本”并利用分层、异构特征识别,NSB-H2GAN更有效地捕获每个补丁的独特特征,从而提高了千兆像素wsi的表示。我们在CAMELYON16、TCGA-NSCLC和TCGA-COAD三个公开可用的数据集上评估了NSB-H2GAN的性能。结果表明,NSB-H2GAN在定性和定量评估方面都明显优于现有的最先进的方法。此外,NSB-H2GAN生成更详细和可解释的热图,允许精确定位微小病变,小到200\mu m\乘以200\mu m$,这通常被人眼忽略。NSB-H2GAN的强大性能为计算机辅助病理诊断提供了新的范例,并具有推进计算病理学临床应用的巨大潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
NSB-H2GAN: “Negative Sample”-Boosted Hierarchical Heterogeneous Graph Attention Network for Interpretable Classification of Whole-Slide Images
Gigapixel whole-slide image (WSI) prediction and region-of-interest localization present considerable challenges due to the diverse range of features both across different slides and within individual slides. Most current methods rely on weakly supervised learning using homogeneous graphs to establish context-aware relevance within slides, often neglecting the rich diversity of heterogeneous information inherent in pathology images. Inspired by the negative sampling strategy of the Determinantal Point Process (DPP) and the hierarchical structure of pathology slides, we introduce the Negative Sample Boosted Hierarchical Heterogeneous Graph Attention Network (NSB-H2GAN). This model addresses the over-smoothing issue typically encountered in classical Graph Convolutional Networks (GCNs) when applied to pathology slides. By incorporating “negative samples” at multiple scales and utilizing hierarchical, heterogeneous feature discrimination, NSB-H2GAN more effectively captures the unique features of each patch, leading to an improved representation of gigapixel WSIs. We evaluated the performance of NSB-H2GAN on three publicly available datasets: CAMELYON16, TCGA-NSCLC and TCGA-COAD. The results show that NSB-H2GAN significantly outperforms existing state-of-the-art methods in both qualitative and quantitative evaluations. Moreover, NSB-H2GAN generates more detailed and interpretable heatmaps, allowing for precise localization of tiny lesions as small as $200\mu m\times 200\mu m$ that are often missed by the human eye. The robust performance of NSB-H2GAN offers a new paradigm for computer-aided pathology diagnosis and holds great potential for advancing the clinical applications of computational pathology.
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