Context.-Mitotic rate counting is essential in pathologic evaluations in melanoma. The American Joint Committee on Cancer recommends reporting the number of mitotic figures (MFs) in a 1-mm2 area encompassing the ''hot spot.'' There is currently no standard procedure for delineating a 1-mm2 region of interest for MF counting on a digital whole slide image (WSI) of melanoma. Objective.-To establish a standardized method to enclose a 1-mm2 region of interest for MF counting in melanoma based on WSIs and assess the method's effectiveness. Design.-Whole slide images were visualized using the ImageScope viewer (Aperio). Different monitors and viewing magnifications were explored and the annotation tools provided by ImageScope were evaluated. For validation, we compared mitotic rates obtained from WSIs with our method and those from glass slides with traditional microscopy with 30 melanoma cases. Results.-Of the monitors we examined, a 32-inch monitor with 3840 3 2160 resolution was optimal for counting MFs within a 1-mm2 region of interest in melanoma. When WSIs were viewed in the ImageScope viewer, 310 to 320 magnification during screening could efficiently locate a hot spot and 320 to 340 magnification during counting could accurately identify MFs. Fixed-shape annotations with 500 3 500-lm squares or circles can precisely and efficiently enclose a 1-mm2 region of interest. Our method on WSIs was able to produce a higher mitotic rate than with glass slides. Conclusions.-Whole slide images may be used to efficiently count MFs. We recommend fixed-shape annotation with 500 3 500-lm squares or circles for routine practice in counting MFs for melanoma.
CITATION STYLE
Wang, M., Aung, P. P., & Prieto, V. G. (2021). Standardized method for defining a 1-mm2 region of interest for calculation of mitotic rate on melanoma whole slide images. Archives of Pathology and Laboratory Medicine, 145(10), 1255–1263. https://doi.org/10.5858/arpa.2020-0137-OA
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