Observer Performance in the Use of Digital and Optical Microscopy for the Interpretation of Tissue-Based Biomarkers

Background. We conducted a validation study of digital pathology for the quantitative assessment of tissue-based biomarkers with immunohistochemistry. Objective. To examine observer agreement as a function of viewing modality (digital versus optical microscopy), whole slide versus tissue microarray...

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Main Authors: Marios A. Gavrielides, Catherine Conway, Neil O’Flaherty, Brandon D. Gallas, Stephen M. Hewitt
Format: Article
Language:English
Published: Wiley 2014-01-01
Series:Analytical Cellular Pathology
Online Access:http://dx.doi.org/10.1155/2014/157308
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author Marios A. Gavrielides
Catherine Conway
Neil O’Flaherty
Brandon D. Gallas
Stephen M. Hewitt
author_facet Marios A. Gavrielides
Catherine Conway
Neil O’Flaherty
Brandon D. Gallas
Stephen M. Hewitt
author_sort Marios A. Gavrielides
collection DOAJ
description Background. We conducted a validation study of digital pathology for the quantitative assessment of tissue-based biomarkers with immunohistochemistry. Objective. To examine observer agreement as a function of viewing modality (digital versus optical microscopy), whole slide versus tissue microarray (TMA) review, biomarker type (HER2 incorporating membranous staining and Ki-67 with nuclear staining), and data type (continuous and categorical). Methods. Eight pathologists reviewed 50 breast cancer whole slides (25 stained with HER2 and 25 with Ki-67) and 2 TMAs (1 stained with HER2, 1 with Ki-67, each containing 97 cores), using digital and optical microscopy. Results. Results showed relatively high overall interobserver and intermodality agreement, with different patterns specific to biomarker type. For HER2, there was better interobserver agreement for optical compared to digital microscopy for whole slides as well as better interobserver and intermodality agreement for TMAs. For Ki-67, those patterns were not observed. Conclusions. The differences in agreement patterns when examining different biomarkers and different scoring methods and reviewing whole slides compared to TMA stress the need for validation studies focused on specific pathology tasks to eliminate sources of variability that might dilute findings. The statistical uncertainty observed in our analyses calls for adequate sampling for each individual task rather than pooling cases.
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spelling doaj-art-27e052b017a342adb16571518d840cb62025-02-03T06:05:38ZengWileyAnalytical Cellular Pathology2210-71772210-71852014-01-01201410.1155/2014/157308157308Observer Performance in the Use of Digital and Optical Microscopy for the Interpretation of Tissue-Based BiomarkersMarios A. Gavrielides0Catherine Conway1Neil O’Flaherty2Brandon D. Gallas3Stephen M. Hewitt4Division of Imaging, Diagnostics, and Software Reliability, Office of Science and Engineering Laboratories, Center for Devices and Radiological Health, U.S. Food and Drug Administration, Silver Spring, MD 20993, USALaboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USADivision of Imaging, Diagnostics, and Software Reliability, Office of Science and Engineering Laboratories, Center for Devices and Radiological Health, U.S. Food and Drug Administration, Silver Spring, MD 20993, USADivision of Imaging, Diagnostics, and Software Reliability, Office of Science and Engineering Laboratories, Center for Devices and Radiological Health, U.S. Food and Drug Administration, Silver Spring, MD 20993, USALaboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USABackground. We conducted a validation study of digital pathology for the quantitative assessment of tissue-based biomarkers with immunohistochemistry. Objective. To examine observer agreement as a function of viewing modality (digital versus optical microscopy), whole slide versus tissue microarray (TMA) review, biomarker type (HER2 incorporating membranous staining and Ki-67 with nuclear staining), and data type (continuous and categorical). Methods. Eight pathologists reviewed 50 breast cancer whole slides (25 stained with HER2 and 25 with Ki-67) and 2 TMAs (1 stained with HER2, 1 with Ki-67, each containing 97 cores), using digital and optical microscopy. Results. Results showed relatively high overall interobserver and intermodality agreement, with different patterns specific to biomarker type. For HER2, there was better interobserver agreement for optical compared to digital microscopy for whole slides as well as better interobserver and intermodality agreement for TMAs. For Ki-67, those patterns were not observed. Conclusions. The differences in agreement patterns when examining different biomarkers and different scoring methods and reviewing whole slides compared to TMA stress the need for validation studies focused on specific pathology tasks to eliminate sources of variability that might dilute findings. The statistical uncertainty observed in our analyses calls for adequate sampling for each individual task rather than pooling cases.http://dx.doi.org/10.1155/2014/157308
spellingShingle Marios A. Gavrielides
Catherine Conway
Neil O’Flaherty
Brandon D. Gallas
Stephen M. Hewitt
Observer Performance in the Use of Digital and Optical Microscopy for the Interpretation of Tissue-Based Biomarkers
Analytical Cellular Pathology
title Observer Performance in the Use of Digital and Optical Microscopy for the Interpretation of Tissue-Based Biomarkers
title_full Observer Performance in the Use of Digital and Optical Microscopy for the Interpretation of Tissue-Based Biomarkers
title_fullStr Observer Performance in the Use of Digital and Optical Microscopy for the Interpretation of Tissue-Based Biomarkers
title_full_unstemmed Observer Performance in the Use of Digital and Optical Microscopy for the Interpretation of Tissue-Based Biomarkers
title_short Observer Performance in the Use of Digital and Optical Microscopy for the Interpretation of Tissue-Based Biomarkers
title_sort observer performance in the use of digital and optical microscopy for the interpretation of tissue based biomarkers
url http://dx.doi.org/10.1155/2014/157308
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