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血和脑脊液中中枢神经系统淋巴瘤的诊断标志物:系统评价。

Diagnostic markers for CNS lymphoma in blood and cerebrospinal fluid: a systematic review.

机构信息

University Medical Center Utrecht, Utrecht, The Netherlands.

Stichting Epilepsie Instellingen Nederland (SEIN), Heemstede, The Netherlands.

出版信息

Br J Haematol. 2018 Aug;182(3):384-403. doi: 10.1111/bjh.15410. Epub 2018 May 29.

DOI:10.1111/bjh.15410
PMID:29808930
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6099264/
Abstract

Diagnosing central nervous system (CNS) lymphoma remains a challenge. Most patients have to undergo brain biopsy to obtain tissue for diagnosis, with associated risks of serious complications. Diagnostic markers in blood or cerebrospinal fluid (CSF) could facilitate early diagnosis with low complication rates. We performed a systematic literature search for studies on markers in blood or cerebrospinal fluid for the diagnosis CNS lymphoma and assessed the methodological quality of studies with the Quality Assessment of Diagnostic Accuracy Studies tool (QUADAS-2). We evaluated diagnostic value of the markers at a given threshold, as well as differences between mean or median levels in patients versus control groups. Twenty-five studies were included, reporting diagnostic value for 18 markers in CSF (microRNAs -21, -19b, and -92a, RNU2-1f, CXCL13, interleukins -6, -8, and -10, soluble interleukin-2-receptor, soluble CD19, soluble CD27, tumour necrosis factor-alfa, beta-2-microglobulin, antithrombin III, soluble transmembrane activator and calcium modulator and cyclophilin ligand interactor, soluble B cell maturation antigen, neopterin and osteopontin) and three markers in blood (microRNA-21 soluble CD27, and beta-2-microglobulin). All studies were at considerable risk of bias and there were concerns regarding the applicability of 15 studies. CXCL-13, beta-2-microglobulin and neopterin have the highest potential in diagnosing CNS lymphoma, but further study is still needed before they can be used in clinical practice.

摘要

诊断中枢神经系统(CNS)淋巴瘤仍然具有挑战性。大多数患者需要进行脑活检以获取用于诊断的组织,这会带来严重并发症的风险。血液或脑脊液(CSF)中的诊断标志物可以在低并发症率的情况下促进早期诊断。我们对血液或脑脊液中用于诊断 CNS 淋巴瘤的标志物进行了系统的文献检索,并使用诊断准确性研究质量评估工具(QUADAS-2)评估了研究的方法学质量。我们评估了在给定阈值下标志物的诊断价值,以及患者与对照组之间平均或中位数水平的差异。共纳入 25 项研究,报告了 CSF 中 18 种标志物(microRNAs-21、-19b 和 -92a、RNU2-1f、CXCL13、白细胞介素-6、-8 和 -10、可溶性白细胞介素-2 受体、可溶性 CD19、可溶性 CD27、肿瘤坏死因子-α、β-2-微球蛋白、抗凝血酶 III、可溶性跨膜激活剂和钙调节剂及环孢素配体相互作用物、可溶性 B 细胞成熟抗原、新蝶呤和骨桥蛋白)和血液中 3 种标志物(microRNA-21、可溶性 CD27 和β-2-微球蛋白)的诊断价值。所有研究都存在相当大的偏倚风险,有 15 项研究的适用性令人担忧。CXCL-13、β-2-微球蛋白和新蝶呤在诊断 CNS 淋巴瘤方面具有最大的潜力,但在将它们应用于临床实践之前,仍需要进一步的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e39/6099264/6c9ff8d0ba8f/BJH-182-384-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e39/6099264/6c9ff8d0ba8f/BJH-182-384-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e39/6099264/6c9ff8d0ba8f/BJH-182-384-g001.jpg

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