AI allows pre-screening of FGFR3 mutational status using routine histology slides of muscle-invasive bladder cancer.

Bannier PA, Saillard C, Mann P, Touzot M, Maussion C, Matek C, Klümper N, Breyer J, Wirtz R, Sikic D, Schmitz-Dräger B, Wullich B, Hartmann A, Försch S, Eckstein M (2024)


Publication Type: Journal article

Publication year: 2024

Journal

Book Volume: 15

Journal Issue: 1

DOI: 10.1038/s41467-024-55331-6

Abstract

Pathogenic activating mutations in the fibroblast growth factor receptor 3 (FGFR3) drive disease maintenance and progression in urothelial cancer. 10-15% of muscle-invasive and metastatic urothelial cancer (MIBC/mUC) are FGFR3-mutant. Selective targeting of FGFR3 hotspot mutations with tyrosine kinase inhibitors (e.g., erdafitinib) is approved for mUC and requires FGFR3 mutational testing. However, current testing assays (polymerase chain reaction or next-generation sequencing) necessitate high tissue quality, have long turnover time, and are expensive. To overcome these limitations, we develop a deep-learning model that detects FGFR3 mutations using routine hematoxylin-eosin slides. Encompassing 1222 cases, our study is a large-scale validation of a model prescreening FGFR3 mutations for MIBC and mUC patients. In this work, we demonstrate that our model achieves high sensitivity (>93%) on advanced and metastatic cases while reducing molecular testing by 40% on average, thereby offering a cost-effective and rapid pre-screening tool for identifying patients eligible for FGFR3 targeted therapies.

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How to cite

APA:

Bannier, P.A., Saillard, C., Mann, P., Touzot, M., Maussion, C., Matek, C.,... Eckstein, M. (2024). AI allows pre-screening of FGFR3 mutational status using routine histology slides of muscle-invasive bladder cancer. Nature Communications, 15(1). https://doi.org/10.1038/s41467-024-55331-6

MLA:

Bannier, Pierre Antoine, et al. "AI allows pre-screening of FGFR3 mutational status using routine histology slides of muscle-invasive bladder cancer." Nature Communications 15.1 (2024).

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