Image analysis with deep learning to predict breast cancer grade, ER status, histologic subtype, and intrinsic subtype
Open accessAbstract
Abstract RNA-based, multi-gene molecular assays are available and widely used for patients with ER-positive/HER2-negative breast cancers. However, RNA-based genomic tests can be costly and are not available in many countries. Methods for inferring molecular subtype from histologic images may identify patients most likely to benefit from further genomic testing. To identify patients who could benefit from molecular testing based on H&E stained histologic images, we developed an image analysis approach using deep learning. A training set of 571 breast tumors was used to create image-based classifiers for tumor grade, ER status, PAM50 intrinsic subtype, histologic subtype, and risk of recurrence score (ROR-PT). The resulting classifiers were applied to an independent test set ( n = 288), and accuracy, sensitivity, and specificity of each was assessed on the test set. Histologic image analysis with deep learning distinguished low-intermediate vs. high tumor grade (82% accuracy), ER status (84% accuracy), Basal-like vs. non-Basal-like (77% accuracy), Ductal vs. Lobular (94% accuracy), and high vs. low-medium ROR-PT score (75% accuracy). Sampling considerations in the training set minimized bias in the test set. Incorrect classification of ER status was significantly more common for Luminal B tumors. These data provide proof of principle that molecular marker status, including a critical clinical biomarker (i.e., ER status), can be predicted with accuracy >75% based on H&E features. Image-based methods could be promising for identifying patients with a greater need for further genomic testing, or in place of classically scored variables typically accomplished using human-based scoring.
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Groups have reported deep learning for breast cancer diagnosis and subtyping from H&E slides and for quantifying features such as mitotic cell counting.
“groups have reported on the use of deep learning for breast cancer diagnosis and subtyping from H&E slides (49)(50)(51), and quantifying other clinically relevant features such as mitotic cell counting (52,53).”
From Artificial Intelligence in Oncology: Current Landscape, Challenges, and Future Directions (2024) · cites this paper as [51]
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References 41 · Cited by 327
Research works printed but not linked: 3
- [24]Rosen, P. P. Rosen’s Breast Pathology. Wolters Kluwer Health/Lippincott Williams & Wilkins, Philadelphia (2009).
- [28]Allott EH Performance of three-biomarker immunohistochemistry for intrinsic breast cancer subtyping in the AMBER consortium Cancer Epidemiol. Biomark. Prev. 2016 25 470 478 10.1158/1055-9965.EPI-15-0874 PMC4779705 26711328 · DOI
- [34]Simonyan, K. & Zisserman, A. Very deep convolutional networks for large-scale image recognition. in International Conference on Learning Representations, San Diego, California (2015).
- Authors
- Couture, H. D., Williams, L. A., Geradts, J., Nyante, S. J., Butler, E. N., Marron, J. S., Perou, C. M., Troester, M. A., & Niethammer, M.
- Affiliations
- University of North Carolina at Chapel Hill (US)
- Dana-Farber Cancer Institute (US)
- Corresponding author
- Couture, Heather D.
- ORCID
- Venue
- npj Breast Cancer
- Published
- 2018-09-03
- Volume
- 4
- Issue
- 1
- Pages
- 30-30
- ISSN
- 2374-4677 (ISSN-L)
- PMC
- PMC6120869
- OpenAlex
- W2889089723
- Cited by
- 327
- References
- 41
- Citations by year
- 2026: 31 · 2025: 43 · 2024: 60 · 2023: 49 · 2022: 49 · 2021: 47 · 2020: 34 · 2019: 13 · 2018: 1
- FWCI
- 13.38
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- npj Breast Cancer (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Carolina Digital Repository (University of North Carolina at Chapel Hill) (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- UNC Libraries
- Funders
- Breast Cancer Research Foundation
- Nvidia (Tesla K40)
- National Cancer Institute (U01CA179715, CA179715, CA148761, CA-58223, P50 CA 58223, P50CA058223, R01CA148761)
- Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill (LCCC2017T204)
- Topics
- Physical Sciences › Computer Science › Artificial Intelligence › AI in cancer detection
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Radiomics and Machine Learning in Medical Imaging
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Breast Cancer Treatment Studies
- Keywords
- breast cancer, deep learning, tumor grade prediction, estrogen receptor status, PAM50 molecular subtypes, histological subtypes, recurrence risk score, HER2-negative breast cancer, estrogen receptor-positive breast cancer, basal-like breast cancer, luminal B, H&E staining
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