Pati Pushpak, Jaume Guillaume, Foncubierta-Rodríguez Antonio, Feroce Florinda, Anniciello Anna Maria, Scognamiglio Giosue, Brancati Nadia, Fiche Maryse, Dubruc Estelle, Riccio Daniel, Di Bonito Maurizio, De Pietro Giuseppe, Botti Gerardo, Thiran Jean-Philippe, Frucci Maria, Goksel Orcun, Gabrani Maria
IBM Zurich Research Lab, Zurich, Switzerland; Computer-Assisted Applications in Medicine, ETH Zurich, Zurich, Switzerland.
IBM Zurich Research Lab, Zurich, Switzerland; Signal Processing Laboratory 5, EPFL, Lausanne, Switzerland.
Med Image Anal. 2022 Jan;75:102264. doi: 10.1016/j.media.2021.102264. Epub 2021 Oct 27.
Cancer diagnosis, prognosis, and therapy response predictions from tissue specimens highly depend on the phenotype and topological distribution of constituting histological entities. Thus, adequate tissue representations for encoding histological entities is imperative for computer aided cancer patient care. To this end, several approaches have leveraged cell-graphs, capturing the cell-microenvironment, to depict the tissue. These allow for utilizing graph theory and machine learning to map the tissue representation to tissue functionality, and quantify their relationship. Though cellular information is crucial, it is incomplete alone to comprehensively characterize complex tissue structure. We herein treat the tissue as a hierarchical composition of multiple types of histological entities from fine to coarse level, capturing multivariate tissue information at multiple levels. We propose a novel multi-level hierarchical entity-graph representation of tissue specimens to model the hierarchical compositions that encode histological entities as well as their intra- and inter-entity level interactions. Subsequently, a hierarchical graph neural network is proposed to operate on the hierarchical entity-graph and map the tissue structure to tissue functionality. Specifically, for input histology images, we utilize well-defined cells and tissue regions to build HierArchical Cell-to-Tissue (HACT) graph representations, and devise HACT-Net, a message passing graph neural network, to classify the HACT representations. As part of this work, we introduce the BReAst Carcinoma Subtyping (BRACS) dataset, a large cohort of Haematoxylin & Eosin stained breast tumor regions-of-interest, to evaluate and benchmark our proposed methodology against pathologists and state-of-the-art computer-aided diagnostic approaches. Through comparative assessment and ablation studies, our proposed method is demonstrated to yield superior classification results compared to alternative methods as well as individual pathologists. The code, data, and models can be accessed at https://github.com/histocartography/hact-net.
基于组织样本的癌症诊断、预后及治疗反应预测高度依赖于构成组织学实体的表型和拓扑分布。因此,对组织学实体进行编码的适当组织表示对于计算机辅助癌症患者护理至关重要。为此,有几种方法利用细胞图来捕捉细胞微环境,从而描绘组织。这些方法允许利用图论和机器学习将组织表示映射到组织功能,并量化它们之间的关系。尽管细胞信息至关重要,但仅凭它不足以全面表征复杂的组织结构。我们在此将组织视为从精细到粗糙层次的多种组织学实体的分层组合,在多个层次上捕捉多变量组织信息。我们提出了一种新颖的组织样本多级分层实体图表示法,以对将组织学实体及其实体内和实体间水平相互作用进行编码的分层组合进行建模。随后,提出了一种分层图神经网络,用于在分层实体图上运行,并将组织结构映射到组织功能。具体而言,对于输入的组织学图像,我们利用定义明确的细胞和组织区域来构建分层细胞到组织(HACT)图表示,并设计了HACT-Net,一种消息传递图神经网络,用于对HACT表示进行分类。作为这项工作的一部分,我们引入了乳腺癌亚型分类(BRACS)数据集,这是一大组苏木精和伊红染色的乳腺肿瘤感兴趣区域,以针对病理学家和最先进的计算机辅助诊断方法评估和基准测试我们提出的方法。通过比较评估和消融研究,结果表明我们提出的方法与替代方法以及个别病理学家相比,能产生更优的分类结果。代码、数据和模型可在https://github.com/histocartography/hact-net上获取。