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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

Zhuoyan Shen

Mikaël Simard

Douglas Brand

Vanghelita Andrei

Ali Al-Khader

Fatine Oumlil

Katherine Trevers

Thomas Butters

Simon Haefliger

Eleanna Kara

Fernanda Amary

Roberto Tirabosco

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 (12.1 Mb)
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Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/

Copyright Statement
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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