循环肿瘤DNA
结直肠癌
体细胞
癌症
DNA
突变体
生物
核酸
突变
癌症研究
基因
医学
肿瘤科
遗传学
作者
Frank Diehl,Kerstin Schmidt,Michael A. Choti,Katharine Romans,Steven N. Goodman,Meng Li,Katherine A. Thornton,Nishant Agrawal,Lori J. Sokoll,Steve Szabo,Kenneth W. Kinzler,Bert Vogelstein,Luis A. Díaz
出处
期刊:Nature Medicine
[Springer Nature]
日期:2008-07-31
卷期号:14 (9): 985-990
被引量:2321
摘要
The measurement of circulating nucleic acids has transformed the management of chronic viral infections such as HIV. The development of analogous markers for individuals with cancer could similarly enhance the management of their disease. DNA containing somatic mutations is highly tumor specific and thus, in theory, can provide optimum markers. However, the number of circulating mutant gene fragments is small compared to the number of normal circulating DNA fragments, making it difficult to detect and quantify them with the sensitivity required for meaningful clinical use. In this study, we applied a highly sensitive approach to quantify circulating tumor DNA (ctDNA) in 162 plasma samples from 18 subjects undergoing multimodality therapy for colorectal cancer. We found that ctDNA measurements could be used to reliably monitor tumor dynamics in subjects with cancer who were undergoing surgery or chemotherapy. We suggest that this personalized genetic approach could be generally applied to individuals with other types of cancer ( pages 914–915 ).
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