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Automated HER2 Scoring in Breast Cancer Images Using Deep Learning and Pyramid Sampling.
- Source :
-
BME frontiers [BME Front] 2024 Jul 23; Vol. 5, pp. 0048. Date of Electronic Publication: 2024 Jul 23 (Print Publication: 2024). - Publication Year :
- 2024
-
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.<br />Competing Interests: Competing interests: The authors declare that they have no competing interests.<br /> (Copyright © 2024 Sahan Yoruc Selcuk et al.)
Details
- Language :
- English
- ISSN :
- 2765-8031
- Volume :
- 5
- Database :
- MEDLINE
- Journal :
- BME frontiers
- Publication Type :
- Academic Journal
- Accession number :
- 39045139
- Full Text :
- https://doi.org/10.34133/bmef.0048