Barroso, Vincenzo Mitchell
ORCID: 0009-0006-7961-089X, Weng, Zhilong
ORCID: 0009-0002-0321-9406, Glamann, Lennert, Bauer, Marcus, Wickenhauser, Claudia, Zander, Thomas
ORCID: 0000-0002-4266-6818, Büttner, Reinhard
ORCID: 0000-0001-8806-4786, Quaas, Alexander
ORCID: 0000-0002-3537-6011 and Tolkach, Yuri
ORCID: 0000-0001-5239-2841
(2025).
Artificial Intelligence–Based Single-Cell Analysis as a Next-Generation Histologic Grading Approach in Colorectal Cancer: Prognostic Role and Tumor Biology Assessment.
Modern Pathology, 38 (7).
pp. 1-11.
Elsevier.
ISSN 08933952
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PIIS0893395225000675.pdf Bereitstellung unter der CC-Lizenz: Creative Commons Attribution. Download (4MB) |
Abstract
[Artikel-Nr.: 100771] The management of colorectal carcinoma (CRC) relies on pathological interpretation. Digital pathology approaches allow for development of new potent artificial intelligence–based prognostic parameters. The study aimed to develop an artificial intelligence–based image analysis platform allowing fully automatized, quantitative, and explainable tumor microenvironment analysis and extraction of prognostic information from hematoxylin and eosin–stained whole-slide images of CRC patients. Three well--characterized, multi-institutional patient cohorts were included (patient n = 1438, whole-slide image n > 2400). The developed image analysis platform implements quality control and established algorithms to segment tissue and detect cell types. It enabled systematic analysis of immune infiltrate, assessing its prognostic relevance, intratumoral heterogeneity, and biological concepts across multiple survival end points. Analyzing single-cell types and their combinations reveals independent, prognostic parameters, highlighting significant intratumoral heterogeneity, especially in the biopsy setting, which must be accounted for. A key morphologic concept related to tumor control by the immune system is described, resulting in a capable, independent prognostic parameter (tumor “out of control”). Our findings have direct clinical implications and can be used as a foundation for updating the existing CRC grading systems.
| Item Type: | Article |
| Creators: | Creators Email ORCID ORCID Put Code Glamann, Lennert UNSPECIFIED UNSPECIFIED UNSPECIFIED Bauer, Marcus UNSPECIFIED UNSPECIFIED UNSPECIFIED Wickenhauser, Claudia UNSPECIFIED UNSPECIFIED UNSPECIFIED |
| URN: | urn:nbn:de:hbz:38-803505 |
| Identification Number: | 10.1016/j.modpat.2025.100771 |
| Journal or Publication Title: | Modern Pathology |
| Volume: | 38 |
| Number: | 7 |
| Page Range: | pp. 1-11 |
| Number of Pages: | 11 |
| Date: | July 2025 |
| Publisher: | Elsevier |
| ISSN: | 08933952 |
| Language: | English |
| Faculty: | Faculty of Medicine |
| Divisions: | Faculty of Medicine > Innere Medizin > Klinik I für Innere Medizin - Hämatologie und Onkologie Faculty of Medicine > Pathologie und Neuropathologie > Institut für Pathologie |
| Subjects: | Medical sciences Medicine |
| Uncontrolled Keywords: | Keywords Language artificial intelligence ; colorectal cancer ; grading ; hematoxylin and eosin ; prognosis ; single-cell English |
| ['eprint_fieldname_oa_funders' not defined]: | Publikationsfonds UzK |
| Refereed: | Yes |
| URI: | http://kups.ub.uni-koeln.de/id/eprint/80350 |
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https://orcid.org/0009-0006-7961-089X