Clinical Applications of Circulating Tumor Cells and Circulating Tumor DNA as Liquid Biopsy

被引:1210
作者
Alix-Panabieres, Catherine [1 ,2 ]
Pantel, Klaus [3 ]
机构
[1] Univ Med Ctr, Dept Cellular & Tissular Biopathol Tumors, LCCRH, Montpellier, France
[2] Univ Montpellier, IURC, Help Personalized Decis EA2415, Methodol Aspects,IURC, F-34059 Montpellier, France
[3] Univ Med Ctr Hamburg Eppendorf, Dept Tumor Biol, Hamburg, Germany
基金
欧洲研究理事会;
关键词
METASTATIC BREAST-CANCER; ANTI-EGFR THERAPY; ACQUIRED-RESISTANCE; PROSTATE-CANCER; BONE-MARROW; MOLECULAR CHARACTERIZATION; COLORECTAL-CANCER; MUTATIONAL STATUS; HER2; EXPRESSION; PROGNOSTIC ROLE;
D O I
10.1158/2159-8290.CD-15-1483
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
"Liquid biopsy" focusing on the analysis of circulating tumor cells (CTC) and circulating cell-free tumor DNA (ctDNA) in the blood of patients with cancer has received enormous attention because of its obvious clinical implications for personalized medicine. Analyses of CTCs and ctDNA have paved new diagnostic avenues and are, to date, the cornerstones of liquid biopsy diagnostics. The present review focuses on key areas of clinical applications of CTCs and ctDNA, including detection of cancer, prediction of prognosis in patients with curable disease, monitoring systemic therapies, and stratification of patients based on the detection of therapeutic targets or resistance mechanisms. Significance: The application of CTCs and ctDNA for the early detection of cancer is of high public interest, but it faces serious challenges regarding specificity and sensitivity of the current assays. Prediction of prognosis in patients with curable disease can already be achieved in several tumor entities, particularly in breast cancer. Monitoring the success or failure of systemic therapies (i.e., chemotherapy, hormonal therapy, or other targeted therapies) by sequential measurements of CTCs or ctDNA is also feasible. Interventional studies on treatment stratification based on the analysis of CTCs and ctDNA are needed to implement liquid biopsy into personalized medicine. (C) 2016 AACR.
引用
收藏
页码:479 / 491
页数:13
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