Objective: We have upgraded our own original color filtration pixel-by-pixel (CFPP) method (Klonowski et al 2018a Physiol. Meas. 39 034002) to enable not only automatic and rapid assessment of the proliferation index of a tumor or neoplasm but also quick automatic location of hot-spots (regions of interest, ROIs) in immunohistochemically stained microscopic images of neoplasms and tumors.
Approach: Neoplastic cells stain differently from normal cells. By counting in a given window the number of pixels belonging to the given subspaces of (R,G,B) color space which correspond, respectively, to proliferating cells (which are mostly neoplastic) and non-proliferating cells (which are mostly normal) we calculate the local proliferation index in this window. The window is moved all around the whole histopathological virtual slide (WSI) or around a chosen part of the WSI. By adding the respective numbers calculated for all the windows covering the WSI or the chosen part of it one can easily calculate the global proliferation index.
Main results: The method is rapid and does not require the time-consuming step of selecting ROIs manually nor does it need computationally complicated detection of hot-spots, both of which attempt to emulate a pathologist's way of thinking. We apply our method to a set of slide images of diffuse large B-cell lymphoma.
Significance: By appropriate changes in the (R,G,B) color filtration thresholds, our method may be adapted to the analysis of other types of tumors. It may also be adapted for analysis of microscopic images in neuropathology. Because of its rapidity and simplicity it may also used for analysis of series of images to assess local dynamics of image complexity in network physiology applications.