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CXCL13 and CXCL9 CSF Levels in Central Nervous System Lymphoma—Diagnostic, Therapeutic, and Prognostic Relevance

Background: Diagnostic delay and neurologic deterioration are still a problem for the treatment of rapidly progressing CNS lymphoma (CNSL); there is an unmet need for a diagnostic test with a high diagnostic yield and limited risk, minimizing the time to the initiation of effective treatment. Method...

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Autores principales: Masouris, Ilias, Manz, Kirsi, Pfirrmann, Markus, Dreyling, Martin, Angele, Barbara, Straube, Andreas, Langer, Sigrid, Huber, Marion, Koedel, Uwe, Von Baumgarten, Louisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8032970/
https://www.ncbi.nlm.nih.gov/pubmed/33841320
http://dx.doi.org/10.3389/fneur.2021.654543
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author Masouris, Ilias
Manz, Kirsi
Pfirrmann, Markus
Dreyling, Martin
Angele, Barbara
Straube, Andreas
Langer, Sigrid
Huber, Marion
Koedel, Uwe
Von Baumgarten, Louisa
author_facet Masouris, Ilias
Manz, Kirsi
Pfirrmann, Markus
Dreyling, Martin
Angele, Barbara
Straube, Andreas
Langer, Sigrid
Huber, Marion
Koedel, Uwe
Von Baumgarten, Louisa
author_sort Masouris, Ilias
collection PubMed
description Background: Diagnostic delay and neurologic deterioration are still a problem for the treatment of rapidly progressing CNS lymphoma (CNSL); there is an unmet need for a diagnostic test with a high diagnostic yield and limited risk, minimizing the time to the initiation of effective treatment. Methods: In this prospective monocentric study, we analyzed the utility of CXCL13 and CXCL9 as diagnostic, therapeutic and prognostic biomarkers for CNSL. Cerebrospinal fluid (CSF) from 155 consecutive patients admitted with brain lesions of various origins was collected. Levels of CXCL13 and CXCL9 were analyzed by ELISA. Additionally, CSF was analyzed during CNSL disease course (relapse, remission, progress) in 17 patients. Results: CXCL13 and CXCL9 CSF levels were significantly increased in patients with CNSL compared to control patients with lesions of other origin. Using logistic regression and a minimal-p-value approach, a cut-off value of 80 pg/ml for CXCL13 shows high sensitivity (90.7%) and specificity (90.1%) for the diagnosis of active CNSL. CXCL9 at a cut-off value of 84 pg/ml is less sensitive (61.5%) and specific (87.1%). Both cytokines correlate with the clinical course and response to therapy. Conclusions: Our results confirm the excellent diagnostic potential of CXCL13 and introduce CXCL9 as a novel albeit less powerful marker for PCNSL.
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spelling pubmed-80329702021-04-10 CXCL13 and CXCL9 CSF Levels in Central Nervous System Lymphoma—Diagnostic, Therapeutic, and Prognostic Relevance Masouris, Ilias Manz, Kirsi Pfirrmann, Markus Dreyling, Martin Angele, Barbara Straube, Andreas Langer, Sigrid Huber, Marion Koedel, Uwe Von Baumgarten, Louisa Front Neurol Neurology Background: Diagnostic delay and neurologic deterioration are still a problem for the treatment of rapidly progressing CNS lymphoma (CNSL); there is an unmet need for a diagnostic test with a high diagnostic yield and limited risk, minimizing the time to the initiation of effective treatment. Methods: In this prospective monocentric study, we analyzed the utility of CXCL13 and CXCL9 as diagnostic, therapeutic and prognostic biomarkers for CNSL. Cerebrospinal fluid (CSF) from 155 consecutive patients admitted with brain lesions of various origins was collected. Levels of CXCL13 and CXCL9 were analyzed by ELISA. Additionally, CSF was analyzed during CNSL disease course (relapse, remission, progress) in 17 patients. Results: CXCL13 and CXCL9 CSF levels were significantly increased in patients with CNSL compared to control patients with lesions of other origin. Using logistic regression and a minimal-p-value approach, a cut-off value of 80 pg/ml for CXCL13 shows high sensitivity (90.7%) and specificity (90.1%) for the diagnosis of active CNSL. CXCL9 at a cut-off value of 84 pg/ml is less sensitive (61.5%) and specific (87.1%). Both cytokines correlate with the clinical course and response to therapy. Conclusions: Our results confirm the excellent diagnostic potential of CXCL13 and introduce CXCL9 as a novel albeit less powerful marker for PCNSL. Frontiers Media S.A. 2021-03-26 /pmc/articles/PMC8032970/ /pubmed/33841320 http://dx.doi.org/10.3389/fneur.2021.654543 Text en Copyright © 2021 Masouris, Manz, Pfirrmann, Dreyling, Angele, Straube, Langer, Huber, Koedel and Von Baumgarten. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Masouris, Ilias
Manz, Kirsi
Pfirrmann, Markus
Dreyling, Martin
Angele, Barbara
Straube, Andreas
Langer, Sigrid
Huber, Marion
Koedel, Uwe
Von Baumgarten, Louisa
CXCL13 and CXCL9 CSF Levels in Central Nervous System Lymphoma—Diagnostic, Therapeutic, and Prognostic Relevance
title CXCL13 and CXCL9 CSF Levels in Central Nervous System Lymphoma—Diagnostic, Therapeutic, and Prognostic Relevance
title_full CXCL13 and CXCL9 CSF Levels in Central Nervous System Lymphoma—Diagnostic, Therapeutic, and Prognostic Relevance
title_fullStr CXCL13 and CXCL9 CSF Levels in Central Nervous System Lymphoma—Diagnostic, Therapeutic, and Prognostic Relevance
title_full_unstemmed CXCL13 and CXCL9 CSF Levels in Central Nervous System Lymphoma—Diagnostic, Therapeutic, and Prognostic Relevance
title_short CXCL13 and CXCL9 CSF Levels in Central Nervous System Lymphoma—Diagnostic, Therapeutic, and Prognostic Relevance
title_sort cxcl13 and cxcl9 csf levels in central nervous system lymphoma—diagnostic, therapeutic, and prognostic relevance
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8032970/
https://www.ncbi.nlm.nih.gov/pubmed/33841320
http://dx.doi.org/10.3389/fneur.2021.654543
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