Zhuoyan Shen
A deep learning framework deploying segment anything to detect pan-cancer mitotic figures from haematoxylin and eosin-stained slides
Shen, Zhuoyan; Simard, Mikaël; Brand, Douglas; Andrei, Vanghelita; Al-Khader, Ali; Oumlil, Fatine; Trevers, Katherine; Butters, Thomas; Haefliger, Simon; Kara, Eleanna; Amary, Fernanda; Tirabosco, Roberto; Cool, Paul; Royle, Gary; Hawkins, Maria A.; Flanagan, Adrienne M.; Collins-Fekete, Charles-Antoine
Authors
Mikaël Simard
Douglas Brand
Vanghelita Andrei
Ali Al-Khader
Fatine Oumlil
Katherine Trevers
Thomas Butters
Simon Haefliger
Eleanna Kara
Fernanda Amary
Roberto Tirabosco
Professor Wim Cool p.cool@keele.ac.uk
Gary Royle
Maria A. Hawkins
Adrienne M. Flanagan
Charles-Antoine Collins-Fekete
Abstract
Mitotic activity is an important feature for grading several cancer types. However, counting mitotic figures (cells in division) is a time-consuming and laborious task prone to inter-observer variation. Inaccurate recognition of MFs can lead to incorrect grading and hence potential suboptimal treatment. This study presents an artificial intelligence-based approach to detect mitotic figures in digitised whole-slide images stained with haematoxylin and eosin. Advances in this area are hampered by the small size and variety of datasets available. To address this, we create the largest dataset of mitotic figures (N = 74,620), combining an in-house dataset of soft tissue tumours with five open-source datasets. We then employ a two-stage framework, named the Optimised Mitoses Generator Network (OMG-Net), to identify mitotic figures. This framework first deploys the Segment Anything Model to automatically outline cells, followed by an adapted ResNet18 that distinguishes mitotic figures. OMG-Net achieves an F1 score of 0.84 in detecting pan-cancer mitotic figures, including human breast carcinoma, neuroendocrine tumours, and melanoma. It outperforms previous state-of-the-art models in hold-out test sets. To summarise, our study introduces a generalisable data creation and curation pipeline and a high-performance detection model, which can largely contribute to the field of computer-aided mitotic figure detection.
Citation
Shen, Z., Simard, M., Brand, D., Andrei, V., Al-Khader, A., Oumlil, F., Trevers, K., Butters, T., Haefliger, S., Kara, E., Amary, F., Tirabosco, R., Cool, P., Royle, G., Hawkins, M. A., Flanagan, A. M., & Collins-Fekete, C.-A. (in press). A deep learning framework deploying segment anything to detect pan-cancer mitotic figures from haematoxylin and eosin-stained slides. Communications Biology, 7(1), 1674. https://doi.org/10.1038/s42003-024-07398-6
Journal Article Type | Article |
---|---|
Acceptance Date | Dec 12, 2024 |
Online Publication Date | Dec 19, 2024 |
Deposit Date | Jan 8, 2025 |
Publicly Available Date | Jan 8, 2025 |
Journal | Communications Biology |
Print ISSN | 2399-3642 |
Electronic ISSN | 2399-3642 |
Publisher | Nature Research |
Peer Reviewed | Peer Reviewed |
Volume | 7 |
Issue | 1 |
Pages | 1674 |
DOI | https://doi.org/10.1038/s42003-024-07398-6 |
Public URL | https://keele-repository.worktribe.com/output/1020489 |
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A deep learning framework deploying segment anything to detect pan-cancer mitotic figures from haematoxylin and eosin-stained slides
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Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
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