Abstract

In recent years, automatic tissue phenotyping has attracted increasing interest in the Digital Pathology (DP) field. For Colorectal Cancer (CRC), tissue phenotyping can diagnose the cancer and differentiate between different cancer grades. The development of Whole Slide Images (WSIs) has provided the required data for creating automatic tissue phenotyping systems. In this paper, we study different hand-crafted feature-based and deep learning methods using two popular multi-classes CRC-tissue-type databases: Kather-CRC-2016 and CRC-TP. For the hand-crafted features, we use two texture descriptors (LPQ and BSIF) and their combination. In addition, two classifiers are used (SVM and NN) to classify the texture features into distinct CRC tissue types. For the deep learning methods, we evaluate four Convolutional Neural Network (CNN) architectures (ResNet-101, ResNeXt-50, Inception-v3, and DenseNet-161). Moreover, we propose two Ensemble CNN approaches: Mean-Ensemble-CNN and NN-Ensemble-CNN. The experimental results show that the proposed approaches outperformed the hand-crafted feature-based methods, CNN architectures and the state-of-the-art methods in both databases.

Highlights

  • Pathologists have used the microscope to analyze the micro-anatomy of cells and tissues

  • We notice that the combination of Local Phase Quantization (LPQ) and Binarized Statistical Image Features (BSIF) gave better performance for both classifiers (SVM and Neural Network (NN))

  • We proposed two Ensemble deep learning approaches to recognize the Colorectal Cancer (CRC) tissue types

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Summary

Introduction

Pathologists have used the microscope to analyze the micro-anatomy of cells and tissues. The new DP imaging modality is able to digitize the Whole Slide Imaging (WSI), where the glass slides are converted into digital slides that can be viewed, managed, shared and analyzed on a computer monitor [2]. In Colorectal Cancer (CRC), tumor architecture changes during tumor progression [3] and is related to patient prognosis [4]. Quantifying the tissue composition in CRC is a relevant task in histopathology. Tumor heterogeneity occurs both between tumors (intertumor heterogeneity) and within tumors (intra-tumor heterogeneity). Tumor MicroEnvironment (TME) plays a crucial role in the development of Intra-Tumor Heterogeneity (ITH) by the various signals that cells receive from their micro-environment [5]

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