Deep learning-based classification of mesothelioma improves prediction of patient outcome

被引:0
|
作者
Pierre Courtiol
Charles Maussion
Matahi Moarii
Elodie Pronier
Samuel Pilcer
Meriem Sefta
Pierre Manceron
Sylvain Toldo
Mikhail Zaslavskiy
Nolwenn Le Stang
Nicolas Girard
Olivier Elemento
Andrew G. Nicholson
Jean-Yves Blay
Françoise Galateau-Sallé
Gilles Wainrib
Thomas Clozel
机构
[1] Owkin Lab,Department of Biopathology
[2] Owkin,Department of Physiology and Biophysics
[3] Inc.,Department of Histopathology
[4] MESOPATH/MESOBANK Cancer Center Léon Bérard,Department of Medical Oncology
[5] Université de Lyon,undefined
[6] Université Claud Bernard Lyon 1,undefined
[7] Institut du Thorax Curie-Montsouris,undefined
[8] Institut Curie,undefined
[9] Institute for Computational Biomedicine and Caryl and Israel Englander Institute for Precision Medicine,undefined
[10] WorldQuant Initiative for Quantitative Prediction,undefined
[11] Weill Cornell Medicine,undefined
[12] Royal Brompton and Harefield Hospitals NHS Foundation Trust,undefined
[13] and National Heart and Lung Institute,undefined
[14] Imperial College,undefined
[15] Centre Léon Bérard,undefined
来源
Nature Medicine | 2019年 / 25卷
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摘要
Malignant mesothelioma (MM) is an aggressive cancer primarily diagnosed on the basis of histological criteria1. The 2015 World Health Organization classification subdivides mesothelioma tumors into three histological types: epithelioid, biphasic and sarcomatoid MM. MM is a highly complex and heterogeneous disease, rendering its diagnosis and histological typing difficult and leading to suboptimal patient care and decisions regarding treatment modalities2. Here we have developed a new approach—based on deep convolutional neural networks—called MesoNet to accurately predict the overall survival of mesothelioma patients from whole-slide digitized images, without any pathologist-provided locally annotated regions. We validated MesoNet on both an internal validation cohort from the French MESOBANK and an independent cohort from The Cancer Genome Atlas (TCGA). We also demonstrated that the model was more accurate in predicting patient survival than using current pathology practices. Furthermore, unlike classical black-box deep learning methods, MesoNet identified regions contributing to patient outcome prediction. Strikingly, we found that these regions are mainly located in the stroma and are histological features associated with inflammation, cellular diversity and vacuolization. These findings suggest that deep learning models can identify new features predictive of patient survival and potentially lead to new biomarker discoveries.
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页码:1519 / 1525
页数:6
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