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Vascular endothelial growth factor (VEGF) in leptomeningeal metastasis: diagnostic and prognostic value

This study examined the diagnostic and prognostic value of vascular endothelial growth factor (VEGF) levels in the cerebrospinal fluid (CSF) of 39 patients with leptomeningeal metastasis (LM). Vascular endothelial growth factor levels at diagnosis were significantly higher in patients with LM (media...

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Autores principales: Herrlinger, U, Wiendl, H, Renninger, M, Förschler, H, Dichgans, J, Weller, M
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409812/
https://www.ncbi.nlm.nih.gov/pubmed/15213721
http://dx.doi.org/10.1038/sj.bjc.6601953
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author Herrlinger, U
Wiendl, H
Renninger, M
Förschler, H
Dichgans, J
Weller, M
author_facet Herrlinger, U
Wiendl, H
Renninger, M
Förschler, H
Dichgans, J
Weller, M
author_sort Herrlinger, U
collection PubMed
description This study examined the diagnostic and prognostic value of vascular endothelial growth factor (VEGF) levels in the cerebrospinal fluid (CSF) of 39 patients with leptomeningeal metastasis (LM). Vascular endothelial growth factor levels at diagnosis were significantly higher in patients with LM (median 359 pg ml(−1)) than in patients with other neurological diseases (median <25 pg ml(−1)). The specificity of VEGF levels above 250 pg ml(−1) for LM was high (98.3%), while the sensitivity was low (51.4%; 73% for VEGF values above 100 pg ml(−1)). In 49% of the LM patients, particularly with lymphoma or medulloblastoma, VEGF levels were below 250 pg ml(−1) and thus in the range of VEGF levels in other neurological diseases. Vascular endothelial growth factor levels correlated significantly with CSF lactate and albumin. Vascular endothelial growth factor levels mirrored the clinical course with a marked reduction in response to therapy and an increase at relapse in some patients who had serial CSF samples available. Multivariate Cox regression analysis showed VEGF below 100 pg ml(−1) (relative risk (RR)=4.24, P=0.0002) and age below 60 years (RR=2.5, P=0.004) to be associated with longer survival in LM. In conclusion, CSF VEGF levels in LM vary considerably. High VEGF levels have a very high specifity for LM and may help to establish the diagnosis. The role of VEGF as a predictor of outcome should be substantiated in prospective studies.
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spelling pubmed-24098122009-09-10 Vascular endothelial growth factor (VEGF) in leptomeningeal metastasis: diagnostic and prognostic value Herrlinger, U Wiendl, H Renninger, M Förschler, H Dichgans, J Weller, M Br J Cancer Clinical This study examined the diagnostic and prognostic value of vascular endothelial growth factor (VEGF) levels in the cerebrospinal fluid (CSF) of 39 patients with leptomeningeal metastasis (LM). Vascular endothelial growth factor levels at diagnosis were significantly higher in patients with LM (median 359 pg ml(−1)) than in patients with other neurological diseases (median <25 pg ml(−1)). The specificity of VEGF levels above 250 pg ml(−1) for LM was high (98.3%), while the sensitivity was low (51.4%; 73% for VEGF values above 100 pg ml(−1)). In 49% of the LM patients, particularly with lymphoma or medulloblastoma, VEGF levels were below 250 pg ml(−1) and thus in the range of VEGF levels in other neurological diseases. Vascular endothelial growth factor levels correlated significantly with CSF lactate and albumin. Vascular endothelial growth factor levels mirrored the clinical course with a marked reduction in response to therapy and an increase at relapse in some patients who had serial CSF samples available. Multivariate Cox regression analysis showed VEGF below 100 pg ml(−1) (relative risk (RR)=4.24, P=0.0002) and age below 60 years (RR=2.5, P=0.004) to be associated with longer survival in LM. In conclusion, CSF VEGF levels in LM vary considerably. High VEGF levels have a very high specifity for LM and may help to establish the diagnosis. The role of VEGF as a predictor of outcome should be substantiated in prospective studies. Nature Publishing Group 2004-07-19 2004-06-22 /pmc/articles/PMC2409812/ /pubmed/15213721 http://dx.doi.org/10.1038/sj.bjc.6601953 Text en Copyright © 2004 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Clinical
Herrlinger, U
Wiendl, H
Renninger, M
Förschler, H
Dichgans, J
Weller, M
Vascular endothelial growth factor (VEGF) in leptomeningeal metastasis: diagnostic and prognostic value
title Vascular endothelial growth factor (VEGF) in leptomeningeal metastasis: diagnostic and prognostic value
title_full Vascular endothelial growth factor (VEGF) in leptomeningeal metastasis: diagnostic and prognostic value
title_fullStr Vascular endothelial growth factor (VEGF) in leptomeningeal metastasis: diagnostic and prognostic value
title_full_unstemmed Vascular endothelial growth factor (VEGF) in leptomeningeal metastasis: diagnostic and prognostic value
title_short Vascular endothelial growth factor (VEGF) in leptomeningeal metastasis: diagnostic and prognostic value
title_sort vascular endothelial growth factor (vegf) in leptomeningeal metastasis: diagnostic and prognostic value
topic Clinical
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409812/
https://www.ncbi.nlm.nih.gov/pubmed/15213721
http://dx.doi.org/10.1038/sj.bjc.6601953
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