Quantitative Analysis of Benign and Malignant Tumors in Histopathology: Predicting Prostate Cancer Grading Using SVM

An adenocarcinoma is a type of malignant cancerous tissue that forms from a glandular structure in epithelial tissue. Analyzed stained microscopic biopsy images were used to perform image manipulation and extract significant features for support vector machine (SVM) classification, to predict the Gl...

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Main Authors: Subrata Bhattacharjee, Hyeon-Gyun Park, Cho-Hee Kim, Deekshitha Prakash, Nuwan Madusanka, Jae-Hong So, Nam-Hoon Cho, Heung-Kook Choi
Format: Article
Language:English
Published: MDPI AG 2019-07-01
Series:Applied Sciences
Subjects:
Online Access:https://www.mdpi.com/2076-3417/9/15/2969
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author Subrata Bhattacharjee
Hyeon-Gyun Park
Cho-Hee Kim
Deekshitha Prakash
Nuwan Madusanka
Jae-Hong So
Nam-Hoon Cho
Heung-Kook Choi
author_facet Subrata Bhattacharjee
Hyeon-Gyun Park
Cho-Hee Kim
Deekshitha Prakash
Nuwan Madusanka
Jae-Hong So
Nam-Hoon Cho
Heung-Kook Choi
author_sort Subrata Bhattacharjee
collection DOAJ
description An adenocarcinoma is a type of malignant cancerous tissue that forms from a glandular structure in epithelial tissue. Analyzed stained microscopic biopsy images were used to perform image manipulation and extract significant features for support vector machine (SVM) classification, to predict the Gleason grading of prostate cancer (PCa) based on the morphological features of the cell nucleus and lumen. Histopathology biopsy tissue images were used and categorized into four Gleason grade groups, namely Grade 3, Grade 4, Grade 5, and benign. The first three grades are considered malignant. K-means and watershed algorithms were used for color-based segmentation and separation of overlapping cell nuclei, respectively. In total, 400 images, divided equally among the four groups, were collected for SVM classification. To classify the proposed morphological features, SVM classification based on binary learning was performed using linear and Gaussian classifiers. The prediction model yielded an accuracy of 88.7% for malignant vs. benign, 85.0% for Grade 3 vs. Grade 4, 5, and 92.5% for Grade 4 vs. Grade 5. The SVM, based on biopsy-derived image features, consistently and accurately classified the Gleason grading of prostate cancer. All results are comparatively better than those reported in the literature.
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spelling doaj.art-fe131b20e667415bb4a9b3e4b3ef06472022-12-21T18:51:09ZengMDPI AGApplied Sciences2076-34172019-07-01915296910.3390/app9152969app9152969Quantitative Analysis of Benign and Malignant Tumors in Histopathology: Predicting Prostate Cancer Grading Using SVMSubrata Bhattacharjee0Hyeon-Gyun Park1Cho-Hee Kim2Deekshitha Prakash3Nuwan Madusanka4Jae-Hong So5Nam-Hoon Cho6Heung-Kook Choi7Department of Computer Engineering, u-AHRC, Inje University, Gimhae 50834, KoreaDepartment of Computer Engineering, u-AHRC, Inje University, Gimhae 50834, KoreaDepartment of Digital Anti-Aging Healthcare, Inje University, Gimhae 50834, KoreaDepartment of Computer Engineering, u-AHRC, Inje University, Gimhae 50834, KoreaDepartment of Computer Engineering, u-AHRC, Inje University, Gimhae 50834, KoreaDepartment of Digital Anti-Aging Healthcare, Inje University, Gimhae 50834, KoreaDepartment of Pathology, Yonsei University Hospital, Seoul 03722, KoreaDepartment of Computer Engineering, u-AHRC, Inje University, Gimhae 50834, KoreaAn adenocarcinoma is a type of malignant cancerous tissue that forms from a glandular structure in epithelial tissue. Analyzed stained microscopic biopsy images were used to perform image manipulation and extract significant features for support vector machine (SVM) classification, to predict the Gleason grading of prostate cancer (PCa) based on the morphological features of the cell nucleus and lumen. Histopathology biopsy tissue images were used and categorized into four Gleason grade groups, namely Grade 3, Grade 4, Grade 5, and benign. The first three grades are considered malignant. K-means and watershed algorithms were used for color-based segmentation and separation of overlapping cell nuclei, respectively. In total, 400 images, divided equally among the four groups, were collected for SVM classification. To classify the proposed morphological features, SVM classification based on binary learning was performed using linear and Gaussian classifiers. The prediction model yielded an accuracy of 88.7% for malignant vs. benign, 85.0% for Grade 3 vs. Grade 4, 5, and 92.5% for Grade 4 vs. Grade 5. The SVM, based on biopsy-derived image features, consistently and accurately classified the Gleason grading of prostate cancer. All results are comparatively better than those reported in the literature.https://www.mdpi.com/2076-3417/9/15/2969prostate cancerhistopathologymicroscopictissue imagesegmentationmorphologicalquantitativeclassificationSVM
spellingShingle Subrata Bhattacharjee
Hyeon-Gyun Park
Cho-Hee Kim
Deekshitha Prakash
Nuwan Madusanka
Jae-Hong So
Nam-Hoon Cho
Heung-Kook Choi
Quantitative Analysis of Benign and Malignant Tumors in Histopathology: Predicting Prostate Cancer Grading Using SVM
Applied Sciences
prostate cancer
histopathology
microscopic
tissue image
segmentation
morphological
quantitative
classification
SVM
title Quantitative Analysis of Benign and Malignant Tumors in Histopathology: Predicting Prostate Cancer Grading Using SVM
title_full Quantitative Analysis of Benign and Malignant Tumors in Histopathology: Predicting Prostate Cancer Grading Using SVM
title_fullStr Quantitative Analysis of Benign and Malignant Tumors in Histopathology: Predicting Prostate Cancer Grading Using SVM
title_full_unstemmed Quantitative Analysis of Benign and Malignant Tumors in Histopathology: Predicting Prostate Cancer Grading Using SVM
title_short Quantitative Analysis of Benign and Malignant Tumors in Histopathology: Predicting Prostate Cancer Grading Using SVM
title_sort quantitative analysis of benign and malignant tumors in histopathology predicting prostate cancer grading using svm
topic prostate cancer
histopathology
microscopic
tissue image
segmentation
morphological
quantitative
classification
SVM
url https://www.mdpi.com/2076-3417/9/15/2969
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