Title | Deep learning-based classification of mesothelioma improves prediction of patient outcome. |
Publication Type | Journal Article |
Year of Publication | 2019 |
Authors | Courtiol P, Maussion C, Moarii M, Pronier E, Pilcer S, Sefta M, Manceron P, Toldo S, Zaslavskiy M, Le Stang N, Girard N, Elemento O, Nicholson AG, Blay J-Y, Galateau-Sallé F, Wainrib G, Clozel T |
Journal | Nat Med |
Volume | 25 |
Issue | 10 |
Pagination | 1519-1525 |
Date Published | 2019 10 |
ISSN | 1546-170X |
Keywords | Deep Learning, Female, Humans, Lung Neoplasms, Male, Mesothelioma, Neoplasm Grading, Neural Networks, Computer, Prognosis |
Abstract | Malignant mesothelioma (MM) is an aggressive cancer primarily diagnosed on the basis of histological criteria. 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 modalities. 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. |
DOI | 10.1038/s41591-019-0583-3 |
Alternate Journal | Nat. Med. |
PubMed ID | 31591589 |