Circulating tumor DNA testing in advanced non-small cell lung cancer

被引:28
|
作者
Moding, Everett J. [1 ,2 ,3 ]
Diehn, Maximilian [1 ,2 ,3 ]
Wakelee, Heather A. [1 ,4 ]
机构
[1] Stanford Univ, Sch Med, Stanford Canc Inst, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Radiat Oncol, Sch Med, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Inst Stem Cell Biol & Regenerat Med, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Med, Sch Med, Div Oncol, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
Circulating tumor DNA; Liquid biopsy; Biomarker; Non-small cell lung cancer; Epidermal growth factor receptor; Drug resistance; FACTOR RECEPTOR MUTATIONS; PLASMA DNA; ACQUIRED-RESISTANCE; KRAS MUTATIONS; EGFR MUTATIONS; OPEN-LABEL; PHASE-III; 1ST-LINE TREATMENT; NSCLC PATIENTS; GEFITINIB;
D O I
10.1016/j.lungcan.2018.02.019
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Circulating tumor DNA (ctDNA) shed from cancer cells into the peripheral blood can be non-invasively collected and tested for the presence of tumor-specific mutations. Mutations identified in ctDNA can predict responses to targeted therapies and emerging evidence suggests that changes in ctDNA levels over time can be used to monitor response to therapy and detect disease recurrence. Given the emergence of targeted therapies in advanced non-small cell lung cancer (NSCLC), liquid biopsies utilizing ctDNA testing represent a powerful approach to genotype tumors and monitor for the development of resistance. Here, we review current and potential future clinical applications of ctDNA testing for patients with advanced NSCLC.
引用
收藏
页码:42 / 47
页数:6
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