Clatot Florian
Department of Medical Oncology, Centre Henri Becquerel, 1 rue d'Amiens, 76038, Rouen Cedex 1, France.
Normandie Univ, UNIROUEN, Inserm U1245, IRON Group, Normandy Centre for Genomic and Personalized Medicine, Rouen University Hospital, Rouen, France.
Recent Results Cancer Res. 2020;215:231-252. doi: 10.1007/978-3-030-26439-0_12.
In only few years, circulating tumor DNA (ctDNA) in breast cancer has moved from purely fundamental research to nearby daily use for treatment selection and drug-resistance assessment. Indeed, technical advances and widespread use of next-generation sequencing or digital PCR allowed for detection of very low amount of tumor DNA in bloodstream. The use of ctDNA as liquid biopsy able either to monitor tumor burden under treatment or to overcome tumor heterogeneity and identify potential targetable drivers. Time has come to define how ctDNA can be implemented for early or metastatic breast cancer management. Data from retrospective analyses of prospective trials have recently highlighted the potential advantages but also the limitations of ctDNA, in particular for patients under endocrine therapy.
在短短几年内,乳腺癌循环肿瘤DNA(ctDNA)已从单纯的基础研究发展到几乎可用于日常治疗选择和耐药性评估。事实上,技术进步以及下一代测序或数字PCR的广泛应用使得能够检测出血液中极少量的肿瘤DNA。将ctDNA用作液体活检,既可以监测治疗中的肿瘤负荷,也可以克服肿瘤异质性并识别潜在的可靶向驱动因素。现在是时候定义如何将ctDNA应用于早期或转移性乳腺癌的管理了。近期来自前瞻性试验回顾性分析的数据凸显了ctDNA的潜在优势,但也指出了其局限性,尤其是对于接受内分泌治疗的患者。