A deep learning system can accurately classify primary and metastatic cancers based on patterns of passenger mutations
Wei JiaoiD, Gurnit Atwal, Paz Polak, Rosa Karlic, Edwin Cuppen, Alexandra DanyiiD, Jeroen de RidderiD, Carla van Herpen, Martijn P Lolkema, Neeltje SteeghsiD, Gad Getz, Quaid D Morris, Lincoln D. Stein, PCAWG Pathology & Clinical Correlates Working Grp, ICGC/TCGA Pan-cancer Analysis of Whole Genomes Net
Abstract
The two strongest factors predicting a human cancers clinical behaviour are the primary tumours anatomic organ of origin and its histopathology. However, roughly 3% of the time a cancer presents with metastatic disease and no primary can be determined even after a thorough radiological survey. A related dilemma arises when a radiologically defined mass is sampled by cytology yielding cancerous cells, but the cytologist cannot distinguish between a primary tumour and a metastasis from elsewhere.\n\nHere we use whole genome sequencing (WGS) data from the ICGC/TCGA PanCancer Analysis of Whole Genomes (PCAWG) project to develop a machine learning classifier able to accurately distinguish among 23 major cancer types using information derived from somatic mutations alone. This demonstrates the feasibility of automated cancer type discrimination based on next-generation sequencing of clinical samples. In addition, this work opens the possibility of determining the origin of tumours detected by the emerging technology of deep sequencing of circulating cell-free DNA in blood plasma.
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