Journal
DIAGNOSTIC PATHOLOGY
Volume 14, Issue -, Pages -Publisher
BMC
DOI: 10.1186/s13000-019-0839-8
Keywords
Whole slide imaging; Microscopy; eeDAP; Multiple whole slide scanner; Mitotic cell quantification; Validation study
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Funding
- Warren Alpert Foundation Center for Digital and Computational Pathology at Memorial Sloan Kettering Cancer Center
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BackgroundThe establishment of whole-slide imaging (WSI) as a medical diagnostic device allows that pathologists may evaluate mitotic activity with this new technology. Furthermore, the image digitalization provides an opportunity to develop algorithms for automatic quantifications, ideally leading to improved reproducibility as compared to the naked eye examination by pathologists. In order to implement them effectively, accuracy of mitotic figure detection using WSI should be investigated. In this study, we aimed to measure pathologist performance in detecting mitotic figures (MFs) using multiple platforms (multiple scanners) and compare the results with those obtained using a brightfield microscope.MethodsFour slides of canine oral melanoma were prepared and digitized using 4 WSI scanners. In these slides, 40 regions of interest (ROIs) were demarcated, and five observers identified the MFs using different viewing modes: microscopy and WSI. We evaluated the inter- and intra-observer agreements between modes with Cohen's Kappa and determined true MFs with a consensus panel. We then assessed the accuracy (agreement with truth) using the average of sensitivity and specificity.ResultsIn the 40 ROIs, 155 candidate MFs were detected by five pathologists; 74 of them were determined to be true MFs. Inter- and intra-observer agreement was mostly substantial or greater (Kappa=0.594-0.939). Accuracy was between 0.632 and 0.843 across all readers and modes. After averaging over readers for each modality, we found that mitosis detection accuracy for 3 of the 4 WSI scanners was significantly less than that of the microscope (p=0.002, 0.012, and 0.001).ConclusionsThis study is the first to compare WSIs and microscopy in detecting MFs at the level of individual cells. Our results suggest that WSI can be used for mitotic cell detection and offers similar reproducibility to the microscope, with slightly less accuracy.
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