SVM-based Framework for the Robust Extraction of Objects from Histopathological Images Using Color, Texture, Scale and Geometry

The extraction of nuclei from Haematoxylin and Eosin (H&E) stained biopsies present a particularly steep challenge in part due to the irregularity of the high-grade (most malignant) tumors. To your best knowledge, although some existing solutions perform adequately with relatively predictable low-grade cancers, solutions for the problematic high-grade cancers have yet to be proposed. In this paper, we propose a method for the extraction of cell nuclei from H&E stained biopsies robust enough to deal with the full range of histological grades observed in daily clinical practice. The robustness is achieved by combining a wide range of information including color, texture, scale and geometry in a multi-stage, Support Vector Machine (SVM) based framework to replace the original image with a new, probabilistic image modality with stable characteristics. The actual extraction of the nuclei is performed from the new image using Mark Point Processes (MPP), a state-of-the-art stochastic method. An empirical evaluation on clinical data provided and annotated by pathologists shows that our method greatly improves detection and extraction results, and provides a reliable solution with high grade cancers. Moreover, our method based on machine learning can easily adapt to specific clinical conditions. In many respects, our method contributes to bridging the gap between the computer vision technologies and their actual clinical use for breast cancer grading.

[1]  A. Ruifrok,et al.  Comparison of Quantification of Histochemical Staining By Hue-Saturation-Intensity (HSI) Transformation and Color-Deconvolution , 2003, Applied immunohistochemistry & molecular morphology : AIMM.

[2]  Josiane Zerubia,et al.  A Marked Point Process Model with Strong Prior Shape Information for the Extraction of Multiple, Arbitrarily-Shaped Objects , 2009, 2009 Fifth International Conference on Signal Image Technology and Internet Based Systems.

[3]  Metin Nafi Gürcan,et al.  Computer-Aided Detection of Centroblasts for Follicular Lymphoma Grading Using Adaptive Likelihood-Based Cell Segmentation , 2010, IEEE Transactions on Biomedical Engineering.

[4]  C. Duchon Lanczos Filtering in One and Two Dimensions , 1979 .

[5]  Stefan Rüping,et al.  A Simple Method For Estimating Conditional Probabilities For SVMs , 2004, LWA.

[6]  A. Ruifrok,et al.  Quantification of histochemical staining by color deconvolution. , 2001, Analytical and quantitative cytology and histology.

[7]  Xiaobo Zhou,et al.  Nuclei Segmentation Using Marker-Controlled Watershed, Tracking Using Mean-Shift, and Kalman Filter in Time-Lapse Microscopy , 2006, IEEE Transactions on Circuits and Systems I: Regular Papers.

[8]  Chao-Hui Huang,et al.  Nuclear pleomorphism scoring by selective cell nuclei detection , 2009, WACV.

[9]  E. Berg,et al.  World Health Organization Classification of Tumours , 2002 .

[10]  H. Kuhn The Hungarian method for the assignment problem , 1955 .

[11]  K. Laws Textured Image Segmentation , 1980 .

[12]  Daniel Racoceanu,et al.  Nuclei extraction from histopathological images using a marked point process approach , 2012, Medical Imaging.

[13]  Harold W. Kuhn,et al.  The Hungarian method for the assignment problem , 1955, 50 Years of Integer Programming.

[14]  Anant Madabhushi,et al.  Active Contour for Overlap Resolution using Watershed BASED initialization (ACOReW): Applications to histopathology , 2011, 2011 IEEE International Symposium on Biomedical Imaging: From Nano to Macro.