1Mayo Clinic Alix School of Medicine, Rochester.
2Department of Neurological Surgery, Mayo Clinic, Rochester.
Neurosurg Focus. 2022 Dec;53(6):E14. doi: 10.3171/2022.9.FOCUS22430.
Glioblastoma (GBM) is a devasting primary brain tumor with less than a 5% 5-year survival. Treatment response assessment can be challenging because of inflammatory pseudoprogression that mimics true tumor progression clinically and on imaging. Developing additional noninvasive assays is critical. In this article, the authors review various biomarkers that could be used in developing liquid biopsies for GBM, along with strengths, limitations, and future applications. In addition, they present a potential liquid biopsy design based on the use of an extracellular vesicle-based liquid biopsy targeting nonneoplastic extracellular vesicles.
The authors conducted a current literature review of liquid biopsy in GBM by searching the PubMed, Scopus, and Google Scholar databases. Articles were assessed for type of biomarker, isolation methodology, analytical techniques, and clinical relevance.
Recent work has shown that liquid biopsies of plasma, blood, and/or CSF hold promise as noninvasive clinical tools that can be used to diagnose recurrence, assess treatment response, and predict patient outcomes in GBM. Liquid biopsy in GBM has focused primarily on extracellular vesicles, cell-free tumor nucleic acids, and whole-cell isolates as focal biomarkers. GBM tumor signatures have been generated via analysis of tumor gene mutations, unique RNA expression, and metabolic and proteomic alterations. Liquid biopsies capture tumor heterogeneity, identifying alterations in GBM tumors that may be undetectable via surgical biopsy specimens. Finally, biomarker burden can be used to assess treatment response and recurrence in GBM.
Liquid biopsy offers a promising avenue for monitoring treatment response and recurrence in GBM without invasive procedures. Although additional steps must be taken to bring liquid biopsy into the clinic, proof-of-principle studies and isolation methodologies are promising. Ultimately, CSF and/or plasma-based liquid biopsy is likely to be a powerful tool in the neurosurgeon's arsenal in the near future for the treatment and management of GBM patients.
胶质母细胞瘤(GBM)是一种毁灭性的原发性脑肿瘤,其 5 年生存率不到 5%。由于炎症性假性进展在临床上和影像学上模拟了真正的肿瘤进展,因此治疗反应评估具有挑战性。开发额外的非侵入性检测方法至关重要。本文作者综述了可用于开发 GBM 液体活检的各种生物标志物,包括其优势、局限性和未来应用。此外,他们还提出了一种基于利用针对非肿瘤细胞外囊泡的细胞外囊泡液体活检的潜在液体活检设计。
作者通过搜索 PubMed、Scopus 和 Google Scholar 数据库,对 GBM 液体活检的现有文献进行了综述。评估了文章中的生物标志物类型、分离方法、分析技术和临床相关性。
最近的工作表明,血浆、血液和/或 CSF 的液体活检作为非侵入性临床工具具有潜力,可用于诊断复发、评估治疗反应并预测 GBM 患者的预后。GBM 的液体活检主要集中在外泌体、无细胞肿瘤核酸和全细胞分离物等焦点生物标志物上。通过分析肿瘤基因突变、独特的 RNA 表达以及代谢和蛋白质组学改变,生成了 GBM 肿瘤特征。液体活检可捕获肿瘤异质性,确定可能通过手术活检样本无法检测到的 GBM 肿瘤改变。最后,生物标志物负担可用于评估 GBM 中的治疗反应和复发。
液体活检为监测 GBM 的治疗反应和复发提供了一种很有前途的方法,无需进行侵入性操作。尽管还需要采取更多步骤将液体活检引入临床,但初步研究和分离方法很有希望。最终,CSF 和/或血浆液体活检很可能成为神经外科医生在不久的将来治疗和管理 GBM 患者的有力工具。