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基于深度学习的非小细胞肺癌组织病理学图像分类和突变预测。

Classification and mutation prediction from non-small cell lung cancer histopathology images using deep learning.

机构信息

Applied Bioinformatics Laboratories, New York University School of Medicine, New York, NY, USA.

Skirball Institute, Department of Cell Biology, New York University School of Medicine, New York, NY, USA.

出版信息

Nat Med. 2018 Oct;24(10):1559-1567. doi: 10.1038/s41591-018-0177-5. Epub 2018 Sep 17.

DOI:10.1038/s41591-018-0177-5
PMID:30224757
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9847512/
Abstract

Visual inspection of histopathology slides is one of the main methods used by pathologists to assess the stage, type and subtype of lung tumors. Adenocarcinoma (LUAD) and squamous cell carcinoma (LUSC) are the most prevalent subtypes of lung cancer, and their distinction requires visual inspection by an experienced pathologist. In this study, we trained a deep convolutional neural network (inception v3) on whole-slide images obtained from The Cancer Genome Atlas to accurately and automatically classify them into LUAD, LUSC or normal lung tissue. The performance of our method is comparable to that of pathologists, with an average area under the curve (AUC) of 0.97. Our model was validated on independent datasets of frozen tissues, formalin-fixed paraffin-embedded tissues and biopsies. Furthermore, we trained the network to predict the ten most commonly mutated genes in LUAD. We found that six of them-STK11, EGFR, FAT1, SETBP1, KRAS and TP53-can be predicted from pathology images, with AUCs from 0.733 to 0.856 as measured on a held-out population. These findings suggest that deep-learning models can assist pathologists in the detection of cancer subtype or gene mutations. Our approach can be applied to any cancer type, and the code is available at https://github.com/ncoudray/DeepPATH .

摘要

病理学家通过观察组织病理学切片来评估肺肿瘤的分期、类型和亚型,这是主要方法之一。肺腺癌(LUAD)和肺鳞状细胞癌(LUSC)是最常见的肺癌亚型,需要有经验的病理学家通过肉眼观察来区分。在这项研究中,我们在从癌症基因组图谱获得的全切片图像上训练了深度卷积神经网络(inception v3),以准确且自动地将其分类为 LUAD、LUSC 或正常肺组织。我们的方法的性能可与病理学家相媲美,平均曲线下面积(AUC)为 0.97。我们的模型在独立的冷冻组织、福尔马林固定石蜡包埋组织和活检数据集上进行了验证。此外,我们还训练了该网络来预测 LUAD 中最常见的十种突变基因。我们发现其中六种基因-STK11、EGFR、FAT1、SETBP1、KRAS 和 TP53-可以从病理图像中预测,在预留人群中的 AUC 从 0.733 到 0.856 不等。这些发现表明深度学习模型可以帮助病理学家检测癌症亚型或基因突变。我们的方法可以应用于任何癌症类型,代码可在 https://github.com/ncoudray/DeepPATH 上获得。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2034/9847512/41fd42e90c22/nihms-1861775-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2034/9847512/bcdb5479506d/nihms-1861775-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2034/9847512/e0fc8bcfd008/nihms-1861775-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2034/9847512/655674371d12/nihms-1861775-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2034/9847512/41fd42e90c22/nihms-1861775-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2034/9847512/bcdb5479506d/nihms-1861775-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2034/9847512/e0fc8bcfd008/nihms-1861775-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2034/9847512/655674371d12/nihms-1861775-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2034/9847512/41fd42e90c22/nihms-1861775-f0004.jpg

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