TY - GEN
T1 - Unsupervised Nuclei Segmentation Using Spatial Organization Priors
AU - Le Bescond, Loïc
AU - Lerousseau, Marvin
AU - Garberis, Ingrid
AU - André, Fabrice
AU - Christodoulidis, Stergios
AU - Vakalopoulou, Maria
AU - Talbot, Hugues
N1 - Publisher Copyright:
© 2022, The Author(s), under exclusive license to Springer Nature Switzerland AG.
PY - 2022/1/1
Y1 - 2022/1/1
N2 - In digital pathology, various biomarkers (e.g., KI67, HER2, CD3/CD8) are routinely analyzed by pathologists through immuno-histo-chemistry-stained slides. Identifying these biomarkers on patient biopsies allows for a more informed design of their treatment regimen. The diversity and specificity of these types of images make the availability of annotated databases sparse. Consequently, robust and efficient learning-based diagnostic systems are difficult to develop and apply in a clinical setting. Our study builds on the observation that the overall organization and structure of the observed tissues are similar across different staining protocols. In this paper, we propose to leverage both the wide availability of haematoxylin-eosin stained databases and the invariance of tissue organization and structure in order to perform unsupervised nuclei segmentation on immunohistochemistry images. We implement and evaluate a generative adversarial method that relies on high-level nuclei distribution priors through comparison with largely available haematoxylin-eosin stained cell nuclei masks. Our approach shows promising results compared to classic unsupervised and supervised methods, as we quantitatively demonstrate on two publicly available datasets. Our code is publicly available to encourage further contributions (https://github.com/loic-lb/Unsupervised-Nuclei-Segmentation-using-Spatial-Organization-Priors ).
AB - In digital pathology, various biomarkers (e.g., KI67, HER2, CD3/CD8) are routinely analyzed by pathologists through immuno-histo-chemistry-stained slides. Identifying these biomarkers on patient biopsies allows for a more informed design of their treatment regimen. The diversity and specificity of these types of images make the availability of annotated databases sparse. Consequently, robust and efficient learning-based diagnostic systems are difficult to develop and apply in a clinical setting. Our study builds on the observation that the overall organization and structure of the observed tissues are similar across different staining protocols. In this paper, we propose to leverage both the wide availability of haematoxylin-eosin stained databases and the invariance of tissue organization and structure in order to perform unsupervised nuclei segmentation on immunohistochemistry images. We implement and evaluate a generative adversarial method that relies on high-level nuclei distribution priors through comparison with largely available haematoxylin-eosin stained cell nuclei masks. Our approach shows promising results compared to classic unsupervised and supervised methods, as we quantitatively demonstrate on two publicly available datasets. Our code is publicly available to encourage further contributions (https://github.com/loic-lb/Unsupervised-Nuclei-Segmentation-using-Spatial-Organization-Priors ).
KW - Biomedical imaging
KW - Digital pathology
KW - Generative adversarial networks
KW - Precision medicine
UR - http://www.scopus.com/inward/record.url?scp=85139006514&partnerID=8YFLogxK
U2 - 10.1007/978-3-031-16434-7_32
DO - 10.1007/978-3-031-16434-7_32
M3 - Conference contribution
AN - SCOPUS:85139006514
SN - 9783031164330
T3 - Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics)
SP - 325
EP - 335
BT - Medical Image Computing and Computer Assisted Intervention – MICCAI 2022 - 25th International Conference, Proceedings
A2 - Wang, Linwei
A2 - Dou, Qi
A2 - Fletcher, P. Thomas
A2 - Speidel, Stefanie
A2 - Li, Shuo
PB - Springer Science and Business Media Deutschland GmbH
T2 - 25th International Conference on Medical Image Computing and Computer-Assisted Intervention, MICCAI 2022
Y2 - 18 September 2022 through 22 September 2022
ER -