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A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns

In cancer, the primary tumour’s organ of origin and histopathology are the strongest determinants of its clinical behaviour, but in 3% of cases a patient presents with a metastatic tumour and no obvious primary. Here, as part of the ICGC/TCGA Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium,...

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Autores principales: Jiao, Wei, Atwal, Gurnit, Polak, Paz, Karlic, Rosa, Cuppen, Edwin, Danyi, Alexandra, de Ridder, Jeroen, van Herpen, Carla, Lolkema, Martijn P., Steeghs, Neeltje, Getz, Gad, Morris, Quaid D., Stein, Lincoln D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7002586/
https://www.ncbi.nlm.nih.gov/pubmed/32024849
http://dx.doi.org/10.1038/s41467-019-13825-8
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author Jiao, Wei
Atwal, Gurnit
Polak, Paz
Karlic, Rosa
Cuppen, Edwin
Danyi, Alexandra
de Ridder, Jeroen
van Herpen, Carla
Lolkema, Martijn P.
Steeghs, Neeltje
Getz, Gad
Morris, Quaid D.
Stein, Lincoln D.
author_facet Jiao, Wei
Atwal, Gurnit
Polak, Paz
Karlic, Rosa
Cuppen, Edwin
Danyi, Alexandra
de Ridder, Jeroen
van Herpen, Carla
Lolkema, Martijn P.
Steeghs, Neeltje
Getz, Gad
Morris, Quaid D.
Stein, Lincoln D.
author_sort Jiao, Wei
collection PubMed
description In cancer, the primary tumour’s organ of origin and histopathology are the strongest determinants of its clinical behaviour, but in 3% of cases a patient presents with a metastatic tumour and no obvious primary. Here, as part of the ICGC/TCGA Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium, we train a deep learning classifier to predict cancer type based on patterns of somatic passenger mutations detected in whole genome sequencing (WGS) of 2606 tumours representing 24 common cancer types produced by the PCAWG Consortium. Our classifier achieves an accuracy of 91% on held-out tumor samples and 88% and 83% respectively on independent primary and metastatic samples, roughly double the accuracy of trained pathologists when presented with a metastatic tumour without knowledge of the primary. Surprisingly, adding information on driver mutations reduced accuracy. Our results have clinical applicability, underscore how patterns of somatic passenger mutations encode the state of the cell of origin, and can inform future strategies to detect the source of circulating tumour DNA.
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spelling pubmed-70025862020-02-07 A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns Jiao, Wei Atwal, Gurnit Polak, Paz Karlic, Rosa Cuppen, Edwin Danyi, Alexandra de Ridder, Jeroen van Herpen, Carla Lolkema, Martijn P. Steeghs, Neeltje Getz, Gad Morris, Quaid D. Stein, Lincoln D. Nat Commun Article In cancer, the primary tumour’s organ of origin and histopathology are the strongest determinants of its clinical behaviour, but in 3% of cases a patient presents with a metastatic tumour and no obvious primary. Here, as part of the ICGC/TCGA Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium, we train a deep learning classifier to predict cancer type based on patterns of somatic passenger mutations detected in whole genome sequencing (WGS) of 2606 tumours representing 24 common cancer types produced by the PCAWG Consortium. Our classifier achieves an accuracy of 91% on held-out tumor samples and 88% and 83% respectively on independent primary and metastatic samples, roughly double the accuracy of trained pathologists when presented with a metastatic tumour without knowledge of the primary. Surprisingly, adding information on driver mutations reduced accuracy. Our results have clinical applicability, underscore how patterns of somatic passenger mutations encode the state of the cell of origin, and can inform future strategies to detect the source of circulating tumour DNA. Nature Publishing Group UK 2020-02-05 /pmc/articles/PMC7002586/ /pubmed/32024849 http://dx.doi.org/10.1038/s41467-019-13825-8 Text en © The Author(s) 2020, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Jiao, Wei
Atwal, Gurnit
Polak, Paz
Karlic, Rosa
Cuppen, Edwin
Danyi, Alexandra
de Ridder, Jeroen
van Herpen, Carla
Lolkema, Martijn P.
Steeghs, Neeltje
Getz, Gad
Morris, Quaid D.
Stein, Lincoln D.
A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns
title A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns
title_full A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns
title_fullStr A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns
title_full_unstemmed A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns
title_short A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns
title_sort deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7002586/
https://www.ncbi.nlm.nih.gov/pubmed/32024849
http://dx.doi.org/10.1038/s41467-019-13825-8
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