组织学
H&E染色
癌症
表型
病理
数字化病理学
组织病理学
分子诊断学
生物
医学
计算生物学
免疫组织化学
生物信息学
基因
遗传学
作者
Jakob Nikolas Kather,Lara R. Heij,Heike I. Grabsch,Chiara Maria Lavinia Loeffler,Amelie Echle,Hannah Sophie Muti,Jeremias Krause,Jan Niehues,Kai Sommer,Peter Bankhead,Loes Kooreman,Jefree J. Schulte,Nicole A. Cipriani,Roman D. Buelow,Peter Boor,Nadina Ortiz‐Brüchle,Andrew M. Hanby,Valerie Speirs,Sara Kochanny,Akash Patnaik
出处
期刊:Nature cancer
[Nature Portfolio]
日期:2020-07-27
卷期号:1 (8): 789-799
被引量:518
标识
DOI:10.1038/s43018-020-0087-6
摘要
Molecular alterations in cancer can cause phenotypic changes in tumor cells and their microenvironment. 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 5,000 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. Two papers by Kather and colleagues and Gerstung and colleagues develop workflows to predict a wide range of molecular alterations from pan-cancer digital pathology slides.
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