Cerebrospinal fluid cell-free tumour DNA as a liquid biopsy for primary brain tumours and central nervous system metastases

被引:108
作者
Seoane, J. [1 ,2 ,3 ,4 ]
De Mattos-Arruda, L. [1 ]
Le Rhun, E. [5 ,6 ,7 ]
Bardelli, A. [8 ,9 ]
Weller, M. [10 ,11 ]
机构
[1] Vall dHebron Univ Hosp, Vall dHebron Inst Oncol, Barcelona, Spain
[2] ICREA, Barcelona, Spain
[3] CIBERONC, Barcelona, Spain
[4] Univ Autonoma Barcelona, Cerdanyola Del Valles, Spain
[5] Lille Univ, INSERM, U1192, PRISM, Villeneuve Dascq, France
[6] Univ Hosp, Dept Neurosurg, Neurooncol, Lille, France
[7] Ctr Oscar Lambret, Dept Med Oncol, Breast Unit, Neurooncol, Lille, France
[8] IRCCS, Candiolo Canc Inst FPO, Candiolo, TO, Italy
[9] Univ Torino, Dept Oncol, Candiolo, TO, Italy
[10] Univ Hosp, Dept Neurol, Zurich, Switzerland
[11] Univ Zurich, Zurich, Switzerland
基金
欧盟地平线“2020”;
关键词
cerebrospinal fluid; circulating cell-free tumour DNA; glioblastoma; brain metastasis; liquid biopsy; brain cancer; MULTICENTER PHASE-II; BREAST-CANCER; LUNG-CANCER; OPEN-LABEL; LEPTOMENINGEAL CARCINOMATOSIS; MELANOMA METASTASES; RADIATION-THERAPY; ESR1; MUTATIONS; HETEROGENEITY; GLIOBLASTOMA;
D O I
10.1093/annonc/mdy544
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Challenges in obtaining tissue specimens from patients with brain tumours limit the diagnosis and molecular characterisation and impair the development of better therapeutic approaches. The analysis of cell-free tumour DNA in plasma (considered a liquid biopsy) has facilitated the characterisation of extra-cranial tumours. However, cell-free tumour DNA in plasma is limited in quantity and may not reliably capture the landscape of genomic alterations of brain tumours. Here, we review recent work assessing the relevance of cell-free tumour DNA from cerebrospinal fluid in the characterisation of brain cancer. We focus on the advances in the use of the cerebrospinal fluid as a source of cell-free tumour DNA to facilitate diagnosis, reveal actionable genomic alterations, monitor responses to therapy, and capture tumour heterogeneity in patients with primary brain tumours and brain and leptomeningeal metastases. Profiling cerebrospinal fluid cell-free tumour DNA provides the opportunity to precisely acquire and monitor genomic information in real time and guide precision therapies.
引用
收藏
页码:211 / 218
页数:8
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