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Spatially Aware Cell Cluster(SpACCl) Graphs: Predicting Outcome in Oropharyngeal p16+ Tumors

机译:空间感知细胞簇(SpACCl)图:预测口咽p16 +肿瘤的结果

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Quantitative measurements of spatial arrangement of nuclei in histopathology images for different cancers has been shown to have prognostic value. Traditionally, graph algorithms (with celluclei as node) have been used to characterize the spatial arrangement of these cells. However, these graphs inherently extract only global features of cell or nuclear architecture and, therefore, important information at the local level may be left unexploited. Additionally, since the graph construction does not draw a distinction between nuclei in the stroma or epithelium, the graph edges often traverse the stromal and epithelial regions. In this paper, we present a new spatially aware cell cluster (SpACCl) graph that can efficiently and accurately model local nuclear interactions, separately within the stromal and epithelial regions alone. SpACCl is built locally on nodes that are defined on groups/clusters of nuclei rather than individual nuclei. Local nodes are connected with edges which have a certain probability of connectedness. The SpACCl graph allows for exploration of (a) contribution of nuclear arrangement within the stromal and epithelial regions separately and (b) combined contribution of stromal and epithelial nuclear architecture in predicting disease aggressiveness and patient outcome. In a cohort of 160 p16+ oropharyngeal tumors (141 non-progressors and 19 progressors), a support vector machine (SVM) classifier in conjunction with 7 graph features extracted from the SpACCl graph yielded a mean accuracy of over 90% with PPV of 89.4% in distinguishing between progressors and non-progressors. Our results suggest that (a) stromal nuclear architecture has a role to play in predicting disease aggressiveness and that (b) combining nuclear architectural contributions from the stromal and epithelial regions yields superior prognostic accuracy compared to individual contributions from stroma and epithelium alone.
机译:已显示对不同癌症的组织病理学图像中核的空间排列进行定量测量具有预后价值。传统上,已使用图算法(以细胞/细胞核为节点)来表征这些细胞的空间排列。但是,这些图固有地仅提取细胞或核结构的全局特征,因此,可能无法利用本地的重要信息。另外,由于图的构造没有区分基质或上皮中的核,因此图的边缘通常横穿基质和上皮区域。在本文中,我们提出了一个新的空间感知细胞簇(SpACCl)图,该图可以有效而准确地模拟局部核相互作用,单独在基质和上皮区域内。 SpACC1本地构建在节点的组/簇上定义的节点上,而不是在单个原子核上定义。局部节点与具有一定连通可能性的边缘相连。 SpACCl图允许探索(a)基质和上皮区域内核排列的贡献,以及(b)基质和上皮核结构的组合贡献,以预测疾病的侵袭性和患者预后。在一组160个p16 +口咽肿瘤(141个非进展性患者和19个进展性患者)中,支持向量机(SVM)分类器与从SpACCl图中提取的7个图特征相结合,产生了90%以上的平均准确度,PPV为89.4%区分进步者和非进步者。我们的研究结果表明:(a)基质核结构在预测疾病的侵袭性中可以发挥作用;(b)结合基质和上皮区域的核结构贡献,与单独基质和上皮的贡献相比,可提供更好的预后准确性。

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