Abstract

High-resolution microscopy images of tissue specimens provide detailed information about the morphology of normal and diseased tissue. Image analysis of tissue morphology can help cancer researchers develop a better understanding of cancer biology. Segmentation of nuclei and classification of tissue images are two common tasks in tissue image analysis. Development of accurate and efficient algorithms for these tasks is a challenging problem because of the complexity of tissue morphology and tumor heterogeneity. In this paper we present two computer algorithms; one designed for segmentation of nuclei and the other for classification of whole slide tissue images. The segmentation algorithm implements a multiscale deep residual aggregation network to accurately segment nuclear material and then separate clumped nuclei into individual nuclei. The classification algorithm initially carries out patch-level classification via a deep learning method, then patch-level statistical and morphological features are used as input to a random forest regression model for whole slide image classification. The segmentation and classification algorithms were evaluated in the MICCAI 2017 Digital Pathology challenge. The segmentation algorithm achieved an accuracy score of 0.78. The classification algorithm achieved an accuracy score of 0.81. These scores were the highest in the challenge.

Highlights

  • Cancer causes changes in tissue at the sub-cellular scale

  • In this paper we present and experimentally evaluate two novel algorithms, one devised for segmentation of nuclei and the other developed for classification of whole slide tissue images:

  • An evaluation of the segmentation algorithm using a set of image tiles from glioblastoma multiforme (GBM), lower grade glioma (LGG), head and neck squamous cell carcinoma (HNSCC), and non-small cell lung cancer (NSCLC) cases showed that the algorithm was able to achieve a segmentation accuracy of 0.78

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Summary

Introduction

Cancer causes changes in tissue at the sub-cellular scale. Pathologists examine a tissue specimen under a powerful microscope to look for abnormalities which indicate cancer. This manual process has traditionally been the de facto standard for diagnosis and grading of cancer tumors. While it continues to be widely applied in clinical settings, manual examination of tissue is a subjective, qualitative analysis and is not scalable to translational and clinical research studies involving hundreds or thousands of tissue specimens. A quantitative analysis of normal and tumor tissue, on the other hand, can provide novel insights into observed and latent sub-cellular tissue

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