Kang Keiko M, Muralidharan Koushik, Yekula Anudeep, Small Julia L, Rosh Zachary S, Jones Pamela S, Carter Bob S, Balaj Leonora
Department of Neurosurgery, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02115, USA.
School of Medicine, University of California San Diego, San Diego, CA 92092, USA.
Cancers (Basel). 2021 Mar 11;13(6):1227. doi: 10.3390/cancers13061227.
Liquid biopsy provides a minimally invasive platform for the detection of tumor-derived information, including hotspot mutations, such as BRAF V600E. In this study, we provide evidence of the technical development of a ddPCR assay for the detection of BRAF V600E mutations in the plasma of patients with glioma or brain metastasis. In a small patient cohort ( = 9, = 5 BRAF V600E, = 4 BRAF WT, = 4 healthy control), we were able to detect the BRAF V600E mutation in the plasma of 4/5 patients with BRAF V600E-tissue confirmed mutant tumors, and none of the BRAF WT tumors. We also provide evidence in two metastatic patients with longitudinal monitoring, where the plasma-based BRAF V600E mutation correlated with clinical disease status. This proof of principle study demonstrates the potential of this assay to serve as an adjunctive tool for the detection, monitoring, and molecular characterization of BRAF mutant gliomas and brain metastasis.
液体活检为检测肿瘤衍生信息提供了一个微创平台,这些信息包括热点突变,如BRAF V600E。在本研究中,我们提供了一种用于检测胶质瘤或脑转移患者血浆中BRAF V600E突变的ddPCR检测技术发展的证据。在一个小患者队列(n = 9,其中n = 5为BRAF V600E突变,n = 4为BRAF野生型,n = 4为健康对照)中,我们能够在4/5组织确诊为BRAF V600E突变肿瘤的患者血浆中检测到BRAF V600E突变,而BRAF野生型肿瘤患者血浆中均未检测到。我们还提供了两名转移患者纵向监测的证据,其中基于血浆的BRAF V600E突变与临床疾病状态相关。这项原理验证研究证明了该检测方法作为BRAF突变型胶质瘤和脑转移的检测、监测及分子特征分析辅助工具的潜力。