1Department of Neurosurgery, Johns Hopkins Hospital, Baltimore, Maryland; and.
2Stanford University School of Medicine, Stanford, California.
Neurosurg Focus. 2020 Jan 1;48(1):E9. doi: 10.3171/2019.9.FOCUS19699.
Diffuse midline glioma (DMG) is a highly malignant childhood tumor with an exceedingly poor prognosis and limited treatment options. The majority of these tumors harbor somatic mutations in genes encoding histone variants. These recurrent mutations correlate with treatment response and are forming the basis for molecularly guided clinical trials. The ability to detect these mutations, either in circulating tumor DNA (ctDNA) or cerebrospinal fluid tumor DNA (CSF-tDNA), may enable noninvasive molecular profiling and earlier prediction of treatment response. Here, the authors review ctDNA and CSF-tDNA detection methods, detail recent studies that have explored detection of ctDNA and CSF-tDNA in patients with DMG, and discuss the implications of liquid biopsies for patients with DMG.
弥漫性中线脑胶质瘤(DMG)是一种高度恶性的儿童肿瘤,预后极差,治疗选择有限。这些肿瘤大多数都存在组蛋白变异体编码基因的体细胞突变。这些反复出现的突变与治疗反应相关,并为分子指导的临床试验提供了基础。无论是在循环肿瘤 DNA(ctDNA)还是脑脊液肿瘤 DNA(CSF-tDNA)中检测到这些突变的能力,都可能实现非侵入性的分子分析,并更早地预测治疗反应。在这里,作者回顾了 ctDNA 和 CSF-tDNA 的检测方法,详细介绍了最近探索 DMG 患者 ctDNA 和 CSF-tDNA 检测的研究,并讨论了液体活检对 DMG 患者的意义。