Khurana Sakshi, Nie Qian, Schilter Kala F, Reddi Honey V
Belay Diagnostics, 1375 W. Fulton St, Chicago, IL, 60607, USA.
J Liq Biopsy. 2025 Jul 25;9:100317. doi: 10.1016/j.jlb.2025.100317. eCollection 2025 Sep.
Meta-analysis of literature was performed to gain an understanding of the performance of genomic profiling assays in cerebrospinal fluid (CSF) for the diagnosis and management of CNS cancers.
Using PRISMA methodology, PubMed was searched with the following search terms; "CSF and liquid biopsy" and "cerebrospinal fluid, liquid biopsy, mutations." Key data fields such as DNA input, technologies used, biomarkers evaluated, types of CNS tumors, sensitivity and specificity, and performance outcomes were analyzed. Studies were excluded if they did not evaluate cancer, use CSF or molecular test methods, had <10 patients, involved pediatric cases or were review articles.
A total of 63 studies were included in the analysis with a majority using ctDNA (n = 38) and targeted NGS panels (n = 45) with both sensitivity and specificity being reported in 24 studies. Of the samples sequenced, 76 % of the primary cancers were gliomas with lung cancer making up 67 % of the metastatic cancers. The Belay Summit™ test performed significantly better in both primary and metastatic CNS cancers with 88 % and 95 % sensitivity respectively compared to studies that used NGS with 6 of the 24 demonstrating a median sensitivity of 47 ± 1.95 % for primary and 7 of 24 demonstrating a median sensitivity of 71 ± 0.76 % for metastatic cancers.
CSF does have potential to inform treatment and management of CNS tumors. For a CSF based molecular test to be highly sensitive and specific, key considerations include panel content, methodology used, the type of variants being evaluated and the inclusion of true negative controls.
进行文献荟萃分析,以了解脑脊液(CSF)基因组分析检测在中枢神经系统(CNS)癌症诊断和管理中的性能。
采用PRISMA方法,在PubMed中使用以下检索词进行检索:“CSF与液体活检”以及“脑脊液、液体活检、突变”。分析了DNA输入、所用技术、评估的生物标志物、CNS肿瘤类型、敏感性和特异性以及性能结果等关键数据字段。如果研究未评估癌症、未使用CSF或分子检测方法、患者少于10例、涉及儿科病例或为综述文章,则将其排除。
共有63项研究纳入分析,大多数研究使用ctDNA(n = 38)和靶向NGS面板(n = 45),24项研究报告了敏感性和特异性。在测序的样本中,原发性癌症的76%为胶质瘤,肺癌占转移性癌症的67%。与使用NGS的研究相比,Belay Summit™检测在原发性和转移性CNS癌症中表现明显更好,敏感性分别为88%和95%,24项研究中有6项显示原发性癌症的中位敏感性为47±1.95%,24项研究中有7项显示转移性癌症的中位敏感性为71±0.76%。
CSF确实有可能为CNS肿瘤的治疗和管理提供信息。要使基于CSF的分子检测具有高度敏感性和特异性,关键考虑因素包括检测面板内容、所用方法、评估的变异类型以及纳入真正的阴性对照。