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

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 complica...

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Autores principales: van Westrhenen, Anouk, Smidt, Lisanne C. A., Seute, Tatjana, Nierkens, Stefan, Stork, Abraham C. J., Minnema, Monique C., Snijders, Tom J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099264/
https://www.ncbi.nlm.nih.gov/pubmed/29808930
http://dx.doi.org/10.1111/bjh.15410
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author van Westrhenen, Anouk
Smidt, Lisanne C. A.
Seute, Tatjana
Nierkens, Stefan
Stork, Abraham C. J.
Minnema, Monique C.
Snijders, Tom J.
author_facet van Westrhenen, Anouk
Smidt, Lisanne C. A.
Seute, Tatjana
Nierkens, Stefan
Stork, Abraham C. J.
Minnema, Monique C.
Snijders, Tom J.
author_sort van Westrhenen, Anouk
collection PubMed
description 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.
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spelling pubmed-60992642018-08-23 Diagnostic markers for CNS lymphoma in blood and cerebrospinal fluid: a systematic review van Westrhenen, Anouk Smidt, Lisanne C. A. Seute, Tatjana Nierkens, Stefan Stork, Abraham C. J. Minnema, Monique C. Snijders, Tom J. Br J Haematol Haematological Malignancy 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. John Wiley and Sons Inc. 2018-05-29 2018-08 /pmc/articles/PMC6099264/ /pubmed/29808930 http://dx.doi.org/10.1111/bjh.15410 Text en © 2018 The Authors. British Journal of Haematology published by John Wiley & Sons Ltd and British Society for Haematology. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Haematological Malignancy
van Westrhenen, Anouk
Smidt, Lisanne C. A.
Seute, Tatjana
Nierkens, Stefan
Stork, Abraham C. J.
Minnema, Monique C.
Snijders, Tom J.
Diagnostic markers for CNS lymphoma in blood and cerebrospinal fluid: a systematic review
title Diagnostic markers for CNS lymphoma in blood and cerebrospinal fluid: a systematic review
title_full Diagnostic markers for CNS lymphoma in blood and cerebrospinal fluid: a systematic review
title_fullStr Diagnostic markers for CNS lymphoma in blood and cerebrospinal fluid: a systematic review
title_full_unstemmed Diagnostic markers for CNS lymphoma in blood and cerebrospinal fluid: a systematic review
title_short Diagnostic markers for CNS lymphoma in blood and cerebrospinal fluid: a systematic review
title_sort diagnostic markers for cns lymphoma in blood and cerebrospinal fluid: a systematic review
topic Haematological Malignancy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099264/
https://www.ncbi.nlm.nih.gov/pubmed/29808930
http://dx.doi.org/10.1111/bjh.15410
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