Riviere-Cazaux Cecile, Keough Michael B, Zuccato Jeffrey A, Kumar Rahul, Schulz Sebastian, Warrington Arthur E, Ruff Michael W, Ellingson Benjamin M, Sanai Nader, Campian Jian L, Kizilbash Sani H, Parney Ian F, Zadeh Gelareh, Khasraw Mustafa, Kessler Tobias, Sener Ugur, Cahill Daniel P, Mansouri Alireza, Burns Terry C
Department of Neurological Surgery, Mayo Clinic, Rochester, MN, USA.
Division of Neurosurgery, Department of Surgery, University of Toronto, Toronto, Ontario, Canada.
Neuro Oncol. 2025 Jun 21;27(5):1165-1179. doi: 10.1093/neuonc/noae276.
Cerebrospinal fluid (CSF) has emerged as a valuable liquid biopsy source for glioma biomarker discovery and validation. CSF produced within the ventricles circulates through the subarachnoid space, where the composition of glioma-derived analytes is influenced by the proximity and anatomical location of sampling relative to tumor, in addition to underlying tumor biology. The substantial gradients observed between lumbar and intracranial CSF compartments for tumor-derived analytes underscore the importance of sampling site selection. Moreover, radiographic features, such as tumor-CSF contact and blood-brain barrier disruption, are critical covariates that may affect biomarker detection and the abundance of plasma-derived analytes in CSF, respectively. Longitudinal intracranial CSF sampling, enabled by access devices like Ommaya reservoirs, may offer a window into treatment response and disease progression, though variability in analyte yield, sample volumes, and the dynamic effects of surgical resection pose challenges. This review critically evaluates the anatomic, radiographic, and longitudinal factors, or "time-space continuum," that impact glioma CSF biomarker abundance. Practical considerations for longitudinal CSF biobanking, including access device placement and collection, are also reviewed. Key takeaways and recommendations for CSF glioma biomarker discovery and validation are provided as a "hitchhiker's guide" based on our collective experience, along with resources for investigators aiming to develop CSF biobanking at their institutions.
脑脊液(CSF)已成为用于胶质瘤生物标志物发现和验证的重要液体活检来源。脑室内产生的脑脊液在蛛网膜下腔循环,在那里,除了潜在的肿瘤生物学特性外,胶质瘤衍生分析物的组成还受相对于肿瘤的采样距离和解剖位置的影响。在腰椎和颅内脑脊液腔室之间观察到的肿瘤衍生分析物的显著梯度突出了采样部位选择的重要性。此外,影像学特征,如肿瘤与脑脊液的接触以及血脑屏障破坏,分别是可能影响生物标志物检测和脑脊液中血浆衍生分析物丰度的关键协变量。通过像奥马亚储液器这样的接入装置实现的颅内脑脊液纵向采样,可能为治疗反应和疾病进展提供一个窗口,尽管分析物产量、样本量的变异性以及手术切除的动态影响带来了挑战。本综述批判性地评估了影响胶质瘤脑脊液生物标志物丰度的解剖学、影像学和纵向因素,即“时空连续体”。还综述了纵向脑脊液生物样本库的实际考虑因素,包括接入装置的放置和采集。基于我们的集体经验,提供了脑脊液胶质瘤生物标志物发现和验证的关键要点及建议,作为一份“指南”,同时为旨在在其机构开展脑脊液生物样本库建设的研究人员提供了相关资源。