4.6 Article

SuperHistopath: A Deep Learning Pipeline for Mapping Tumor Heterogeneity on Low-Resolution Whole-Slide Digital Histopathology Images

Journal

FRONTIERS IN ONCOLOGY
Volume 10, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fonc.2020.586292

Keywords

deep learning; machine learning; digital pathology; computational pathology; tumor region classification; melanoma; neuroblastoma; breast cancer

Categories

Funding

  1. Rosetrees Trust [M593]
  2. ISCIII (FIS)
  3. FEDER (European Regional Development Fund) [PI17/01558, CB16/12/00484]
  4. Cancer Research UK Career Establishment Award [C45982/A21808]
  5. Breast Cancer Now [2015NovPR638]
  6. Children's Cancer and Leukaemia Group [CCLGA201906]
  7. NIH [U54 CA217376, R01 CA185138]
  8. CDMRP Breast Cancer Research Program [BC132057]
  9. CRUK Brain Tumor Awards (TARGET-GBM)
  10. European Commission ITN (H2020-MSCA-ITN-2019)
  11. Wellcome Trust [105104/Z/14/Z]
  12. Royal Marsden/ICR National Institute of Health Research Biomedical Research Centre
  13. Children with Cancer UK [2014/176]

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SuperHistopath is an efficient framework for digital pathology image analysis which combines segmentation and classification methods to accurately map the heterogeneity of tumor morphologies. It can classify different types of tissues accurately and discover significant differences in research.
High computational cost associated with digital pathology image analysis approaches is a challenge towards their translation in routine pathology clinic. Here, we propose a computationally efficient framework (SuperHistopath), designed to map global context features reflecting the rich tumor morphological heterogeneity. SuperHistopath efficiently combines i) a segmentation approach using the linear iterative clustering (SLIC) superpixels algorithm applied directly on the whole-slide images at low resolution (5x magnification) to adhere to region boundaries and form homogeneous spatial units at tissue-level, followed by ii) classification of superpixels using a convolution neural network (CNN). To demonstrate how versatile SuperHistopath was in accomplishing histopathology tasks, we classified tumor tissue, stroma, necrosis, lymphocytes clusters, differentiating regions, fat, hemorrhage and normal tissue, in 127 melanomas, 23 triple-negative breast cancers, and 73 samples from transgenic mouse models of high-risk childhood neuroblastoma with high accuracy (98.8%, 93.1% and 98.3% respectively). Furthermore, SuperHistopath enabled discovery of significant differences in tumor phenotype of neuroblastoma mouse models emulating genomic variants of high-risk disease, and stratification of melanoma patients (high ratio of lymphocyte-to-tumor superpixels (p = 0.015) and low stroma-to-tumor ratio (p = 0.028) were associated with a favorable prognosis). Finally, SuperHistopath is efficient for annotation of ground-truth datasets (as there is no need of boundary delineation), training and application (similar to 5 min for classifying a whole-slide image and as low as similar to 30 min for network training). These attributes make SuperHistopath particularly attractive for research in rich datasets and could also facilitate its adoption in the clinic to accelerate pathologist workflow with the quantification of phenotypes, predictive/prognosis markers.

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