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Next-generation lung cancer pathology: Development and validation of diagnostic and prognostic algorithms.

Authors :
Kludt C
Wang Y
Ahmad W
Bychkov A
Fukuoka J
Gaisa N
Kühnel M
Jonigk D
Pryalukhin A
Mairinger F
Klein F
Schultheis AM
Seper A
Hulla W
Brägelmann J
Michels S
Klein S
Quaas A
Büttner R
Tolkach Y
Source :
Cell reports. Medicine [Cell Rep Med] 2024 Sep 17; Vol. 5 (9), pp. 101697. Date of Electronic Publication: 2024 Aug 22.
Publication Year :
2024

Abstract

Non-small cell lung cancer (NSCLC) is one of the most common malignant tumors. In this study, we develop a clinically useful computational pathology platform for NSCLC that can be a foundation for multiple downstream applications and provide immediate value for patient care optimization and individualization. We train the primary multi-class tissue segmentation algorithm on a substantial, high-quality, manually annotated dataset of whole-slide images with lung adenocarcinoma and squamous cell carcinomas. We investigate two downstream applications. NSCLC subtyping algorithm is trained and validated using a large, multi-institutional (n = 6), multi-scanner (n = 5), international cohort of NSCLC cases (slides/patients 4,097/1,527). Moreover, we develop four AI-derived, fully explainable, quantitative, prognostic parameters (based on tertiary lymphoid structure and necrosis assessment) and validate them for different clinical endpoints. The computational platform enables the high-precision, quantitative analysis of H&E-stained slides. The developed prognostic parameters facilitate robust and independent risk stratification of patients with NSCLC.<br />Competing Interests: Declaration of interests The authors declare no competing interests.<br /> (Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
2666-3791
Volume :
5
Issue :
9
Database :
MEDLINE
Journal :
Cell reports. Medicine
Publication Type :
Academic Journal
Accession number :
39178857
Full Text :
https://doi.org/10.1016/j.xcrm.2024.101697