微小残留病
循环肿瘤DNA
计算生物学
生物
DNA测序
基因组
体细胞
深度测序
DNA
癌症
遗传学
基因
白血病
作者
David M. Kurtz,Joanne Soo,Lyron Co Ting Keh,Stefan Alig,Jacob J. Chabon,Brian J. Sworder,André Schultz,Michael C. Jin,Florian Scherer,Andrea Garofalo,Charles Macaulay,Emily G. Hamilton,Binbin Chen,Mari Olsen,Joseph G. Schroers‐Martin,Alexander Craig,Everett J. Moding,Mohammad Shahrokh Esfahani,Chih Long Liu,Ulrich Dührsen
标识
DOI:10.1038/s41587-021-00981-w
摘要
Circulating tumor-derived DNA (ctDNA) is an emerging biomarker for many cancers, but the limited sensitivity of current detection methods reduces its utility for diagnosing minimal residual disease. Here we describe phased variant enrichment and detection sequencing (PhasED-seq), a method that uses multiple somatic mutations in individual DNA fragments to improve the sensitivity of ctDNA detection. Leveraging whole-genome sequences from 2,538 tumors, we identify phased variants and their associations with mutational signatures. We show that even without molecular barcodes, the limits of detection of PhasED-seq outperform prior methods, including duplex barcoding, allowing ctDNA detection in the ppm range in participant samples. We profiled 678 specimens from 213 participants with B cell lymphomas, including serial cell-free DNA samples before and during therapy for diffuse large B cell lymphoma. In participants with undetectable ctDNA after two cycles of therapy using a next-generation sequencing-based approach termed cancer personalized profiling by deep sequencing, an additional 25% have ctDNA detectable by PhasED-seq and have worse outcomes. Finally, we demonstrate the application of PhasED-seq to solid tumors.
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