Cellular community detection for tissue phenotyping in colorectal cancer histology images

被引:97
作者
Javed, Sajid [1 ,6 ]
Mahmood, Arif [2 ]
Fraz, Muhammad Moazam [1 ,5 ]
Koohbanani, Navid Alemi [1 ]
Benes, Ksenija [3 ]
Tsang, Yee-Wah [3 ]
Hewitt, Katherine [3 ]
Epstein, David [4 ]
Snead, David [3 ]
Rajpoot, Nasir [1 ,3 ,7 ]
机构
[1] Univ Warwick, Dept Comp Sci, Coventry CV4 7AL, W Midlands, England
[2] Informat Technol Univ, Dept Comp Sci, Lahore, Pakistan
[3] Univ Hosp Coventry & Warwickshire NHS Trust, Dept Pathol, Coventry CV2 2DX, W Midlands, England
[4] Univ Warwick, Math Inst, Coventry CV4 7AL, W Midlands, England
[5] Natl Univ Sci & Technol, Islamabad, Pakistan
[6] Khalifa Univ, Ctr Autonomous Robot Syst KUCARS, POB 127788, Abu Dhabi, U Arab Emirates
[7] Alan Turing Inst, London, England
基金
英国医学研究理事会;
关键词
Computational pathology; Tissue phenotyping; Tumor microenvironment; Cellular communities; PATHOLOGY; REPRESENTATION; CLASSIFICATION; VALIDATION; ALGORITHM; NETWORKS; STROMA;
D O I
10.1016/j.media.2020.101696
中图分类号
TP18 [人工智能理论];
学科分类号
081104 ; 0812 ; 0835 ; 1405 ;
摘要
Classification of various types of tissue in cancer histology images based on the cellular compositions is an important step towards the development of computational pathology tools for systematic digital profiling of the spatial tumor microenvironment. Most existing methods for tissue phenotyping are limited to the classification of tumor and stroma and require large amount of annotated histology images which are often not available. In the current work, we pose the problem of identifying distinct tissue phenotypes as finding communities in cellular graphs or networks. First, we train a deep neural network for cell detection and classification into five distinct cellular components. Considering the detected nuclei as nodes, potential cell-cell connections are assigned using Delaunay triangulation resulting in a cell-level graph. Based on this cell graph, a feature vector capturing potential cell-cell connection of different types of cells is computed. These feature vectors are used to construct a patch-level graph based on chi-square distance. We map patch-level nodes to the geometric space by representing each node as a vector of geodesic distances from other nodes in the network and iteratively drifting the patch nodes in the direction of positive density gradients towards maximum density regions. The proposed algorithm is evaluated on a publicly available dataset and another new large-scale dataset consisting of 280K patches of seven tissue phenotypes. The estimated communities have significant biological meanings as verified by the expert pathologists. A comparison with current state-of-the-art methods reveals significant performance improvement in tissue phenotyping. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页数:18
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