Breast Biomarkers-Comparison on Whole Section and Tissue Microarray Section

Introduction: Estrogen Receptor (ER), Progesterone Receptor (PR) and Her2/neu are routinely studied markers for breast carcinoma. Analysis of these biomarkers is traditionally done by Immunohistochemistry (IHC) on whole sections. These markers can also be studied on Tissue Microarray (TMA) secti...

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Main Authors: Sneha S Chavan, Savithri Ravindra, MSN Prasad
Format: Article
Language:English
Published: JCDR Research and Publications Private Limited 2017-03-01
Series:Journal of Clinical and Diagnostic Research
Subjects:
Online Access:https://jcdr.net/articles/PDF/9573/25088_CE[Ra1]_F(DK)_PF1(SY_RK)_PFA(RK)_PF2(P_NESY).pdf
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author Sneha S Chavan
Savithri Ravindra
MSN Prasad
author_facet Sneha S Chavan
Savithri Ravindra
MSN Prasad
author_sort Sneha S Chavan
collection DOAJ
description Introduction: Estrogen Receptor (ER), Progesterone Receptor (PR) and Her2/neu are routinely studied markers for breast carcinoma. Analysis of these biomarkers is traditionally done by Immunohistochemistry (IHC) on whole sections. These markers can also be studied on Tissue Microarray (TMA) sections. Tissue microarray is a technique where core samples from different paraffin blocks are arrayed on a single recipient block which can then be cut to yield a single section with multiple cores in it. Aim: To compare ER, PR and Her2/neu on TMA sections with whole sections and to determine the concordance of results between the two methods. Materials and Methods: A TMA block was constructed by punching out 2 mm cores from appropriately marked paraffin blocks of 53 breast carcinoma cases and embedding them in the recipient block. Immunostaining of TMA sections and whole sections were performed for ER, PR and Her2/neu and the results were compared. Statistical analysis was done using chi square test/FisherExact test. Kappa co-efficient, Jaccard Index and G-Index were computed. Results: Infiltrating Ductal Carcinoma-No Special Type (IDCNST) was the predominant type of carcinoma and most of the tumours were of Grade II and III. Majority, 38/53 (71.7%) were ER/PR positive and Her2 negative and 9/53 (17%) cases were triple negative. Good concordance between whole sections and TMA sections were noted with kappa value for ER, PR and Her2/neu being 0.671, 0.754, 1.000 respectively which was statistically significant. Conclusion: Immunostaining for ER, PR and Her2/neu done on TMA section using single 2 mm core were comparable with conventional whole section scores. Thus, TMA is a reliable method for evaluating these biomarkers with the advantage of being time and cost effective.
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spelling doaj.art-ce576b0d4789417aa08b22d778ff74672022-12-21T19:18:30ZengJCDR Research and Publications Private LimitedJournal of Clinical and Diagnostic Research2249-782X0973-709X2017-03-01113EC40EC4410.7860/JCDR/2017/25088.9573Breast Biomarkers-Comparison on Whole Section and Tissue Microarray SectionSneha S Chavan0Savithri Ravindra1MSN Prasad2Postgraduate Student, Department of Pathology, Kempegowda Institute of Medical Sciences, Bengaluru, Karnataka, India.Associate Professor, Department of Pathology, Kempegowda Institute of Medical Sciences, Bengaluru, Karnataka, India.Consultant Pathologist, Department of Pathology, Sri Shankara Cancer Hospital and Research Centre, Bengaluru, Karnataka, India.Introduction: Estrogen Receptor (ER), Progesterone Receptor (PR) and Her2/neu are routinely studied markers for breast carcinoma. Analysis of these biomarkers is traditionally done by Immunohistochemistry (IHC) on whole sections. These markers can also be studied on Tissue Microarray (TMA) sections. Tissue microarray is a technique where core samples from different paraffin blocks are arrayed on a single recipient block which can then be cut to yield a single section with multiple cores in it. Aim: To compare ER, PR and Her2/neu on TMA sections with whole sections and to determine the concordance of results between the two methods. Materials and Methods: A TMA block was constructed by punching out 2 mm cores from appropriately marked paraffin blocks of 53 breast carcinoma cases and embedding them in the recipient block. Immunostaining of TMA sections and whole sections were performed for ER, PR and Her2/neu and the results were compared. Statistical analysis was done using chi square test/FisherExact test. Kappa co-efficient, Jaccard Index and G-Index were computed. Results: Infiltrating Ductal Carcinoma-No Special Type (IDCNST) was the predominant type of carcinoma and most of the tumours were of Grade II and III. Majority, 38/53 (71.7%) were ER/PR positive and Her2 negative and 9/53 (17%) cases were triple negative. Good concordance between whole sections and TMA sections were noted with kappa value for ER, PR and Her2/neu being 0.671, 0.754, 1.000 respectively which was statistically significant. Conclusion: Immunostaining for ER, PR and Her2/neu done on TMA section using single 2 mm core were comparable with conventional whole section scores. Thus, TMA is a reliable method for evaluating these biomarkers with the advantage of being time and cost effective.https://jcdr.net/articles/PDF/9573/25088_CE[Ra1]_F(DK)_PF1(SY_RK)_PFA(RK)_PF2(P_NESY).pdfbreast carcinomaestrogen receptorher2/neu
spellingShingle Sneha S Chavan
Savithri Ravindra
MSN Prasad
Breast Biomarkers-Comparison on Whole Section and Tissue Microarray Section
Journal of Clinical and Diagnostic Research
breast carcinoma
estrogen receptor
her2/neu
title Breast Biomarkers-Comparison on Whole Section and Tissue Microarray Section
title_full Breast Biomarkers-Comparison on Whole Section and Tissue Microarray Section
title_fullStr Breast Biomarkers-Comparison on Whole Section and Tissue Microarray Section
title_full_unstemmed Breast Biomarkers-Comparison on Whole Section and Tissue Microarray Section
title_short Breast Biomarkers-Comparison on Whole Section and Tissue Microarray Section
title_sort breast biomarkers comparison on whole section and tissue microarray section
topic breast carcinoma
estrogen receptor
her2/neu
url https://jcdr.net/articles/PDF/9573/25088_CE[Ra1]_F(DK)_PF1(SY_RK)_PFA(RK)_PF2(P_NESY).pdf
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