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

机译:深度学习系统使用乘客突变模式准确地分类原发性和转移性癌症

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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.
机译:在癌症中,原发性肿瘤的原产儿和组织病理学器官是其临床行为最强的决定因素,但在3%的病例中患者患有α转移性肿瘤,没有明显的主要原发性。在这里,作为全基因组(PCAWG)联盟的ICGC / TCGA泛癌癌症分析的一部分,我们训练深度学习分类器,以预测基于在2606个肿瘤的全基因组测序(WGS)中检测到的体细胞乘客突变模式的癌症类型24 PCAWG联盟产生的常见癌症类型。我们的分类器在独立的初级和转移样品中分别在保持肿瘤样品和88%和83%上实现了91%的准确性,大致增加了训练肿瘤的训练病理学家的准确性,而不知道初级。令人惊讶的是,添加有关驾驶员突变的信息降低了准确性。我们的结果具有临床适用性,强调了体细胞乘客突变的模式编码原产地的细胞状态,并且可以告知未来的策略以检测循环肿瘤DNA的源。

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