Automated HER2 Scoring in Breast Cancer Images Using Deep Learning and Pyramid Sampling

Author:

Selcuk Sahan Yoruc123ORCID,Yang Xilin123,Bai Bijie123,Zhang Yijie123,Li Yuzhu123,Aydin Musa123ORCID,Unal Aras Firat123,Gomatam Aditya123,Guo Zhen123,Angus Darrow Morgan4,Kolodney Goren5,Atlan Karine6,Haran Tal Keidar6,Pillar Nir123,Ozcan Aydogan1237ORCID

Affiliation:

1. Electrical and Computer Engineering Department, University of California, Los Angeles, Los Angeles, CA, USA.

2. Bioengineering Department, University of California, Los Angeles, Los Angeles, CA, USA.

3. California NanoSystems Institute, University of California, Los Angeles, Los Angeles, CA, USA.

4. Department of Pathology and Laboratory Medicine, University of California at Davis, Sacramento, CA, USA.

5. Bnai-Zion Medical Center, Haifa, Israel.

6. Hadassah Hebrew University Medical Center, Jerusalem, Israel.

7. David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, USA.

Abstract

Objective and Impact Statement: Human epidermal growth factor receptor 2 (HER2) is a critical protein in cancer cell growth that signifies the aggressiveness of breast cancer (BC) and helps predict its prognosis. Here, we introduce a deep learning-based approach utilizing pyramid sampling for the automated classification of HER2 status in immunohistochemically (IHC) stained BC tissue images. Introduction: Accurate assessment of IHC-stained tissue slides for HER2 expression levels is essential for both treatment guidance and understanding of cancer mechanisms. Nevertheless, the traditional workflow of manual examination by board-certified pathologists encounters challenges, including inter- and intra-observer inconsistency and extended turnaround times. Methods: Our deep learning-based method analyzes morphological features at various spatial scales, efficiently managing the computational load and facilitating a detailed examination of cellular and larger-scale tissue-level details. Results: This approach addresses the tissue heterogeneity of HER2 expression by providing a comprehensive view, leading to a blind testing classification accuracy of 84.70%, on a dataset of 523 core images from tissue microarrays. Conclusion: This automated system, proving reliable as an adjunct pathology tool, has the potential to enhance diagnostic precision and evaluation speed, and might substantially impact cancer treatment planning.

Funder

NIH

Publisher

American Association for the Advancement of Science (AAAS)

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