Liquid Biopsies: Genotyping Circulating Tumor DNA

被引:1643
|
作者
Diaz, Luis A. [1 ,2 ]
Bardelli, Alberto [3 ,4 ]
机构
[1] Johns Hopkins Univ, Sch Med, Swim Amer Lab, Baltimore, MD USA
[2] Johns Hopkins Univ, Sch Med, Ludwig Ctr Canc Genet & Therapeut, Baltimore, MD USA
[3] Univ Turin, Inst Canc Res & Treatment Candiolo, Candiolo, Italy
[4] Fdn Italiana Ric Canc, Inst Mol Oncol, Milan, Italy
关键词
CELL-FREE DNA; FREE PLASMA DNA; ACQUIRED-RESISTANCE; NUCLEIC-ACIDS; BREAST-CANCER; PRENATAL-DIAGNOSIS; BLOOD-PLASMA; FETAL DNA; HALF-LIFE; MUTATIONS;
D O I
10.1200/JCO.2012.45.2011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Genotyping tumor tissue in search of somatic genetic alterations for actionable information has become routine practice in clinical oncology. Although these sequence alterations are highly informative, sampling tumor tissue has significant inherent limitations; tumor tissue is a single snapshot in time, is subject to selection bias resulting from tumor heterogeneity, and can be difficult to obtain. Cell-free fragments of DNA are shed into the bloodstream by cells undergoing apoptosis or necrosis, and the load of circulating cell-free DNA (cfDNA) correlates with tumor staging and prognosis. Moreover, recent advances in the sensitivity and accuracy of DNA analysis have allowed for genotyping of cfDNA for somatic genomic alterations found in tumors. The ability to detect and quantify tumor mutations has proven effective in tracking tumor dynamics in real time as well as serving as a liquid biopsy that can be used for a variety of clinical and investigational applications not previously possible. (C) 2014 by American Society of Clinical Oncology
引用
收藏
页码:579 / +
页数:9
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