Practical recommendations for using ctDNA in clinical decision making

被引:85
作者
Cohen, Stacey A. [1 ,2 ]
Liu, Minetta C. C. [3 ]
Aleshin, Alexey [3 ]
机构
[1] Fred Hutchinson Canc Ctr, Seattle, WA 98109 USA
[2] Univ Washington, Seattle, WA 98195 USA
[3] Natera, Austin, TX USA
关键词
CIRCULATING-TUMOR DNA; BREAST-CANCER; CARCINOEMBRYONIC ANTIGEN; GUIDELINES; PROGRESSION; RECURRENCE; THERAPY; DISEASE; RISK;
D O I
10.1038/s41586-023-06225-y
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The continuous improvement in cancer care over the past decade has led to a gradual decrease in cancer-related deaths. This is largely attributed to improved treatment and disease management strategies. Early detection of recurrence using blood-based biomarkers such as circulating tumour DNA (ctDNA) is being increasingly used in clinical practice. Emerging real-world data shows the utility of ctDNA in detecting molecular residual disease and in treatment-response monitoring, helping clinicians to optimize treatment and surveillance strategies. Many studies have indicated ctDNA to be a sensitive and specific biomarker for recurrence. However, most of these studies are largely observational or anecdotal in nature, and peer-reviewed data regarding the use of ctDNA are mainly indication-specific. Here we provide general recommendations on the clinical utility of ctDNA and how to interpret ctDNA analysis in different treatment settings, especially in patients with solid tumours. Specifically, we provide an understanding around the implications, strengths and limitations of this novel biomarker and how to best apply the results in clinical practice.
引用
收藏
页码:259 / 268
页数:10
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