| Literature DB >> 33763651 |
Alexander T Pearson1, Tom Luedde2,3, Jakob Nikolas Kather4,5,6, Lara R Heij7,8,9, Heike I Grabsch10,11, Chiara Loeffler4, Amelie Echle4, Hannah Sophie Muti4, Jeremias Krause4, Jan M Niehues4, Kai A J Sommer4, Peter Bankhead12, Loes F S Kooreman10, Jefree J Schulte13, Nicole A Cipriani13, Roman D Buelow9, Peter Boor9, Nadi-Na Ortiz-Brüchle9, Andrew M Hanby11, Valerie Speirs14, Sara Kochanny1, Akash Patnaik1, Andrew Srisuwananukorn15, Hermann Brenner5,16,17, Michael Hoffmeister16, Piet A van den Brandt18, Dirk Jäger5,6, Christian Trautwein4.
Abstract
Molecular alterations in cancer can cause phenotypic changes in tumor cells and their micro-environment. Routine histopathology tissue slides - which are ubiquitously available - can reflect such morphological changes. Here, we show that deep learning can consistently infer a wide range of genetic mutations, molecular tumor subtypes, gene expression signatures and standard pathology biomarkers directly from routine histology. We developed, optimized, validated and publicly released a one-stop-shop workflow and applied it to tissue slides of more than 5000 patients across multiple solid tumors. Our findings show that a single deep learning algorithm can be trained to predict a wide range of molecular alterations from routine, paraffin-embedded histology slides stained with hematoxylin and eosin. These predictions generalize to other populations and are spatially resolved. Our method can be implemented on mobile hardware, potentially enabling point-of-care diagnostics for personalized cancer treatment. More generally, this approach could elucidate and quantify genotype-phenotype links in cancer.Entities:
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Year: 2020 PMID: 33763651 PMCID: PMC7610412 DOI: 10.1038/s43018-020-0087-6
Source DB: PubMed Journal: Nat Cancer ISSN: 2662-1347