Using cell nuclei features to detect colon cancer tissue in hematoxylin and eosin stained slides
Currently, diagnosis of colon cancer is based on manual examination of histopathological images by a pathologist. This can be time consuming and interpretation of the images is subject to inter‐ and intra‐observer variability. This may be improved by introducing a computer‐aided diagnosis (CAD) syst...
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Veröffentlicht in: | Cytometry. Part A 2017-08, Vol.91 (8), p.785-793 |
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description | Currently, diagnosis of colon cancer is based on manual examination of histopathological images by a pathologist. This can be time consuming and interpretation of the images is subject to inter‐ and intra‐observer variability. This may be improved by introducing a computer‐aided diagnosis (CAD) system for automatic detection of cancer tissue within whole slide hematoxylin and eosin (H&E) stains. Cancer disrupts the normal control mechanisms of cell proliferation and differentiation, affecting the structure and appearance of the cells. Therefore, extracting features from segmented cell nuclei structures may provide useful information to detect cancer tissue. A framework for automatic classification of regions of interest (ROI) containing either benign or cancerous colon tissue extracted from whole slide H&E stained images using cell nuclei features was proposed. A total of 1,596 ROI's were extracted from 87 whole slide H&E stains (44 benign and 43 cancer). A cell nuclei segmentation algorithm consisting of color deconvolution, k‐means clustering, local adaptive thresholding, and cell separation was performed within the ROI's to extract cell nuclei features. From the segmented cell nuclei structures a total of 750 texture and intensity‐based features were extracted for classification of the ROI's. The nine most discriminative cell nuclei features were used in a random forest classifier to determine if the ROI's contained benign or cancer tissue. The ROI classification obtained an area under the curve (AUC) of 0.96, sensitivity of 0.88, specificity of 0.92, and accuracy of 0.91 using an optimized threshold. The developed framework showed promising results in using cell nuclei features to classify ROIs into containing benign or cancer tissue in H&E stained tissue samples. © 2017 International Society for Advancement of Cytometry |
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This can be time consuming and interpretation of the images is subject to inter‐ and intra‐observer variability. This may be improved by introducing a computer‐aided diagnosis (CAD) system for automatic detection of cancer tissue within whole slide hematoxylin and eosin (H&E) stains. Cancer disrupts the normal control mechanisms of cell proliferation and differentiation, affecting the structure and appearance of the cells. Therefore, extracting features from segmented cell nuclei structures may provide useful information to detect cancer tissue. A framework for automatic classification of regions of interest (ROI) containing either benign or cancerous colon tissue extracted from whole slide H&E stained images using cell nuclei features was proposed. A total of 1,596 ROI's were extracted from 87 whole slide H&E stains (44 benign and 43 cancer). A cell nuclei segmentation algorithm consisting of color deconvolution, k‐means clustering, local adaptive thresholding, and cell separation was performed within the ROI's to extract cell nuclei features. From the segmented cell nuclei structures a total of 750 texture and intensity‐based features were extracted for classification of the ROI's. The nine most discriminative cell nuclei features were used in a random forest classifier to determine if the ROI's contained benign or cancer tissue. The ROI classification obtained an area under the curve (AUC) of 0.96, sensitivity of 0.88, specificity of 0.92, and accuracy of 0.91 using an optimized threshold. The developed framework showed promising results in using cell nuclei features to classify ROIs into containing benign or cancer tissue in H&E stained tissue samples. © 2017 International Society for Advancement of Cytometry</description><identifier>ISSN: 1552-4922</identifier><identifier>EISSN: 1552-4930</identifier><identifier>DOI: 10.1002/cyto.a.23175</identifier><identifier>PMID: 28727286</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Algorithms ; Area Under Curve ; Benign ; Cancer ; Cell Nucleus - pathology ; Cell proliferation ; cell segmentation ; Classification ; Clustering ; Colon ; Colon cancer ; Colonic Neoplasms - pathology ; Colorectal cancer ; Cytometry ; Diagnosis ; Differentiation ; Eosine Yellowish-(YS) - administration & dosage ; Feature extraction ; H&E stain ; Hematoxylin - administration & dosage ; Humans ; image analysis ; Image Interpretation, Computer-Assisted - methods ; Image processing ; Image segmentation ; Nuclei ; Nuclei (cytology) ; Sensitivity and Specificity ; Staining and Labeling - methods ; Tissues ; Vector quantization</subject><ispartof>Cytometry. 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Part A</title><addtitle>Cytometry A</addtitle><description>Currently, diagnosis of colon cancer is based on manual examination of histopathological images by a pathologist. This can be time consuming and interpretation of the images is subject to inter‐ and intra‐observer variability. This may be improved by introducing a computer‐aided diagnosis (CAD) system for automatic detection of cancer tissue within whole slide hematoxylin and eosin (H&E) stains. Cancer disrupts the normal control mechanisms of cell proliferation and differentiation, affecting the structure and appearance of the cells. Therefore, extracting features from segmented cell nuclei structures may provide useful information to detect cancer tissue. A framework for automatic classification of regions of interest (ROI) containing either benign or cancerous colon tissue extracted from whole slide H&E stained images using cell nuclei features was proposed. A total of 1,596 ROI's were extracted from 87 whole slide H&E stains (44 benign and 43 cancer). A cell nuclei segmentation algorithm consisting of color deconvolution, k‐means clustering, local adaptive thresholding, and cell separation was performed within the ROI's to extract cell nuclei features. From the segmented cell nuclei structures a total of 750 texture and intensity‐based features were extracted for classification of the ROI's. The nine most discriminative cell nuclei features were used in a random forest classifier to determine if the ROI's contained benign or cancer tissue. The ROI classification obtained an area under the curve (AUC) of 0.96, sensitivity of 0.88, specificity of 0.92, and accuracy of 0.91 using an optimized threshold. The developed framework showed promising results in using cell nuclei features to classify ROIs into containing benign or cancer tissue in H&E stained tissue samples. © 2017 International Society for Advancement of Cytometry</description><subject>Algorithms</subject><subject>Area Under Curve</subject><subject>Benign</subject><subject>Cancer</subject><subject>Cell Nucleus - pathology</subject><subject>Cell proliferation</subject><subject>cell segmentation</subject><subject>Classification</subject><subject>Clustering</subject><subject>Colon</subject><subject>Colon cancer</subject><subject>Colonic Neoplasms - pathology</subject><subject>Colorectal cancer</subject><subject>Cytometry</subject><subject>Diagnosis</subject><subject>Differentiation</subject><subject>Eosine Yellowish-(YS) - administration & dosage</subject><subject>Feature extraction</subject><subject>H&E stain</subject><subject>Hematoxylin - administration & dosage</subject><subject>Humans</subject><subject>image analysis</subject><subject>Image Interpretation, Computer-Assisted - methods</subject><subject>Image processing</subject><subject>Image segmentation</subject><subject>Nuclei</subject><subject>Nuclei (cytology)</subject><subject>Sensitivity and Specificity</subject><subject>Staining and Labeling - methods</subject><subject>Tissues</subject><subject>Vector quantization</subject><issn>1552-4922</issn><issn>1552-4930</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kD1PwzAQQC0E4ntjRpZYGGixz3aTjKjiS0JiaQcmYzsXMEptiB1B_z0pBQYGprvh6enuEXLE2ZgzBudumePYjEHwQm2QXa4UjGQl2ObvDrBD9lJ6YUwoJmCb7EBZQAHlZJc8zpMPT9Rh29LQuxY9bdDkvsNEc6Q1ZnSZutjGQJ0JDjuafUo9Uh_oMy5Mjh_LdthNqCnGQUZTNj5gTVPra0wHZKsxbcLD77lP5leXs-nN6O7--nZ6cTdykoEaQWVlU6FkBUqowHJhmwLRTspCcmRWKVGVDNwE6sYCL62zIJRoiomC2iAX--R07X3t4luPKeuFT6u3TMDYJ80r4FxIATCgJ3_Ql9h3YbhuoKTiUkolBupsTbkuptRho187vzDdUnOmV-X1qrw2-qv8gB9_S3u7wPoX_kk9AHINvPsWl__K9PRhdn-x9n4CJEGPow</recordid><startdate>201708</startdate><enddate>201708</enddate><creator>Jørgensen, Alex Skovsbo</creator><creator>Rasmussen, Anders Munk</creator><creator>Andersen, Niels Kristian Mäkinen</creator><creator>Andersen, Simon Kragh</creator><creator>Emborg, Jonas</creator><creator>Røge, Rasmus</creator><creator>Østergaard, Lasse Riis</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201708</creationdate><title>Using cell nuclei features to detect colon cancer tissue in hematoxylin and eosin stained slides</title><author>Jørgensen, Alex Skovsbo ; Rasmussen, Anders Munk ; Andersen, Niels Kristian Mäkinen ; Andersen, Simon Kragh ; Emborg, Jonas ; Røge, Rasmus ; Østergaard, Lasse Riis</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4025-29b4f9e407e4292b13bf7eeb68741e0b5539802c62dfb218bcb2353f7652dae13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Algorithms</topic><topic>Area Under Curve</topic><topic>Benign</topic><topic>Cancer</topic><topic>Cell Nucleus - pathology</topic><topic>Cell proliferation</topic><topic>cell segmentation</topic><topic>Classification</topic><topic>Clustering</topic><topic>Colon</topic><topic>Colon cancer</topic><topic>Colonic Neoplasms - pathology</topic><topic>Colorectal cancer</topic><topic>Cytometry</topic><topic>Diagnosis</topic><topic>Differentiation</topic><topic>Eosine Yellowish-(YS) - administration & dosage</topic><topic>Feature extraction</topic><topic>H&E stain</topic><topic>Hematoxylin - administration & dosage</topic><topic>Humans</topic><topic>image analysis</topic><topic>Image Interpretation, Computer-Assisted - methods</topic><topic>Image processing</topic><topic>Image segmentation</topic><topic>Nuclei</topic><topic>Nuclei (cytology)</topic><topic>Sensitivity and Specificity</topic><topic>Staining and Labeling - methods</topic><topic>Tissues</topic><topic>Vector quantization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jørgensen, Alex Skovsbo</creatorcontrib><creatorcontrib>Rasmussen, Anders Munk</creatorcontrib><creatorcontrib>Andersen, Niels Kristian Mäkinen</creatorcontrib><creatorcontrib>Andersen, Simon Kragh</creatorcontrib><creatorcontrib>Emborg, Jonas</creatorcontrib><creatorcontrib>Røge, Rasmus</creatorcontrib><creatorcontrib>Østergaard, Lasse Riis</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cytometry. Part A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jørgensen, Alex Skovsbo</au><au>Rasmussen, Anders Munk</au><au>Andersen, Niels Kristian Mäkinen</au><au>Andersen, Simon Kragh</au><au>Emborg, Jonas</au><au>Røge, Rasmus</au><au>Østergaard, Lasse Riis</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Using cell nuclei features to detect colon cancer tissue in hematoxylin and eosin stained slides</atitle><jtitle>Cytometry. Part A</jtitle><addtitle>Cytometry A</addtitle><date>2017-08</date><risdate>2017</risdate><volume>91</volume><issue>8</issue><spage>785</spage><epage>793</epage><pages>785-793</pages><issn>1552-4922</issn><eissn>1552-4930</eissn><abstract>Currently, diagnosis of colon cancer is based on manual examination of histopathological images by a pathologist. This can be time consuming and interpretation of the images is subject to inter‐ and intra‐observer variability. This may be improved by introducing a computer‐aided diagnosis (CAD) system for automatic detection of cancer tissue within whole slide hematoxylin and eosin (H&E) stains. Cancer disrupts the normal control mechanisms of cell proliferation and differentiation, affecting the structure and appearance of the cells. Therefore, extracting features from segmented cell nuclei structures may provide useful information to detect cancer tissue. A framework for automatic classification of regions of interest (ROI) containing either benign or cancerous colon tissue extracted from whole slide H&E stained images using cell nuclei features was proposed. A total of 1,596 ROI's were extracted from 87 whole slide H&E stains (44 benign and 43 cancer). A cell nuclei segmentation algorithm consisting of color deconvolution, k‐means clustering, local adaptive thresholding, and cell separation was performed within the ROI's to extract cell nuclei features. From the segmented cell nuclei structures a total of 750 texture and intensity‐based features were extracted for classification of the ROI's. The nine most discriminative cell nuclei features were used in a random forest classifier to determine if the ROI's contained benign or cancer tissue. The ROI classification obtained an area under the curve (AUC) of 0.96, sensitivity of 0.88, specificity of 0.92, and accuracy of 0.91 using an optimized threshold. The developed framework showed promising results in using cell nuclei features to classify ROIs into containing benign or cancer tissue in H&E stained tissue samples. © 2017 International Society for Advancement of Cytometry</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28727286</pmid><doi>10.1002/cyto.a.23175</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Algorithms Area Under Curve Benign Cancer Cell Nucleus - pathology Cell proliferation cell segmentation Classification Clustering Colon Colon cancer Colonic Neoplasms - pathology Colorectal cancer Cytometry Diagnosis Differentiation Eosine Yellowish-(YS) - administration & dosage Feature extraction H&E stain Hematoxylin - administration & dosage Humans image analysis Image Interpretation, Computer-Assisted - methods Image processing Image segmentation Nuclei Nuclei (cytology) Sensitivity and Specificity Staining and Labeling - methods Tissues Vector quantization |
title | Using cell nuclei features to detect colon cancer tissue in hematoxylin and eosin stained slides |
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