Sareen Heena, Garrett Celine, Lynch David, Powter Branka, Brungs Daniel, Cooper Adam, Po Joseph, Koh Eng-Siew, Vessey Joey Yusof, McKechnie Simon, Bazina Renata, Sheridan Mark, Gelder James van, Darwish Balsam, Jaeger Mathias, Roberts Tara L, De Souza Paul, Becker Therese M
Centre for Circulating Tumour Cell Diagnostics and Research, Ingham Institute for Applied Medical Research, 1 Campbell St, Liverpool, NSW 2170, Australia.
South Western Sydney Clinical School, University of New South Wales South Western Clinical School, Goulburn St, Liverpool, NSW 2170, Australia.
Cancers (Basel). 2020 Jul 8;12(7):1831. doi: 10.3390/cancers12071831.
Glioblastoma multiforme (GBM) is one of the most lethal primary central nervous system cancers with a median overall survival of only 12-15 months. The best documented treatment is surgical tumor debulking followed by chemoradiation and adjuvant chemotherapy with temozolomide, but treatment resistance and therefore tumor recurrence, is the usual outcome. Although advances in molecular subtyping suggests GBM can be classified into four subtypes, one concern about using the original histology for subsequent treatment decisions is that it only provides a static snapshot of heterogeneous tumors that may undergo longitudinal changes over time, especially under selective pressure of ongoing therapy. Liquid biopsies obtained from bodily fluids like blood and cerebro-spinal fluid (CSF) are less invasive, and more easily repeated than surgery. However, their deployment for patients with brain cancer is only emerging, and possibly suppressed clinically due to the ongoing belief that the blood brain barrier prevents the egress of circulating tumor cells, exosomes, and circulating tumor nucleic acids into the bloodstream. Although brain cancer liquid biopsy analyses appear indeed challenging, advances have been made and here we evaluate the current literature on the use of liquid biopsies for detection of clinically relevant biomarkers in GBM to aid diagnosis and prognostication.
多形性胶质母细胞瘤(GBM)是最致命的原发性中枢神经系统癌症之一,总体中位生存期仅为12 - 15个月。记录最完善的治疗方法是手术肿瘤切除,随后进行放化疗以及使用替莫唑胺进行辅助化疗,但通常的结果是出现治疗耐药性,进而导致肿瘤复发。尽管分子亚型分类方面的进展表明GBM可分为四种亚型,但对于使用原始组织学来做出后续治疗决策的一个担忧是,它仅提供了异质性肿瘤的静态快照,这些肿瘤可能会随时间发生纵向变化,尤其是在持续治疗的选择压力下。从血液和脑脊液(CSF)等体液中获取的液体活检侵入性较小,且比手术更容易重复进行。然而,它们在脑癌患者中的应用才刚刚兴起,而且可能由于一直以来认为血脑屏障会阻止循环肿瘤细胞、外泌体和循环肿瘤核酸进入血液的观念而在临床上受到抑制。尽管脑癌液体活检分析确实具有挑战性,但已经取得了进展,在此我们评估当前关于使用液体活检检测GBM中临床相关生物标志物以辅助诊断和预后的文献。