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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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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. |
format | Online Article Text |
id | pubmed-6099264 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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