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Malignant Glioma with Neuronal Marker Expression : A Clinicopathological Study of 18 Cases

OBJECTIVE: Malignant gliomas with neuronal marker expression (MGwNM) are rare and poorly characterized. Increasingly diverse types of MGwNM have been described and these reported cases underscore the dilemmas in the classification and diagnosis of those tumors. The aim of this study is to provide ad...

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Autores principales: Kim, Hong Rye, Lee, Jae Jun, Lee, Jung-Il, Nam, Do Hyun, Suh, Yeon-Lim, Seol, Ho Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Neurosurgical Society 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754586/
https://www.ncbi.nlm.nih.gov/pubmed/26885285
http://dx.doi.org/10.3340/jkns.2016.59.1.44
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author Kim, Hong Rye
Lee, Jae Jun
Lee, Jung-Il
Nam, Do Hyun
Suh, Yeon-Lim
Seol, Ho Jun
author_facet Kim, Hong Rye
Lee, Jae Jun
Lee, Jung-Il
Nam, Do Hyun
Suh, Yeon-Lim
Seol, Ho Jun
author_sort Kim, Hong Rye
collection PubMed
description OBJECTIVE: Malignant gliomas with neuronal marker expression (MGwNM) are rare and poorly characterized. Increasingly diverse types of MGwNM have been described and these reported cases underscore the dilemmas in the classification and diagnosis of those tumors. The aim of this study is to provide additional insights into MGwNM and present the clinicopathological features of 18 patients. METHODS: We reviewed the medical records of 18 patients diagnosed as MGwNM at our institute between January 2006 and December 2012. Macroscopic total resection was performed in 11 patients (61%). We evaluated the methylation status of O(6)-methylguanine-DNA methyltransferase (MGMT) and expression of isocitrate dehydrogenase 1 (IDH-1) in all cases, and deletions of 1p and 19q in available cases. RESULTS: The estimated median overall survival was 21.2 months. The median progression-free survival was 6.3 months. Six patients (33%) had MGMT methylation but IDH1 mutation was found in only one patient (6%). Gene analysis for 1p19q performed in nine patients revealed no deletion in six, 19q deletion only in two, and 1p deletion only in one. The extent of resection was significantly correlated with progression free survival on both univariate analysis and multivariate analysis (p=0.002 and p=0.013, respectively). CONCLUSION: In this study, the overall survival of MGwNM was not superior to glioblastoma. The extent of resection has a significant prognostic impact on progression-free survival. Further studies of the prognostic factors related to chemo-radio therapy, similar to studies with glioblastoma, are mandatory to improve survival.
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spelling pubmed-47545862016-02-16 Malignant Glioma with Neuronal Marker Expression : A Clinicopathological Study of 18 Cases Kim, Hong Rye Lee, Jae Jun Lee, Jung-Il Nam, Do Hyun Suh, Yeon-Lim Seol, Ho Jun J Korean Neurosurg Soc Clinical Article OBJECTIVE: Malignant gliomas with neuronal marker expression (MGwNM) are rare and poorly characterized. Increasingly diverse types of MGwNM have been described and these reported cases underscore the dilemmas in the classification and diagnosis of those tumors. The aim of this study is to provide additional insights into MGwNM and present the clinicopathological features of 18 patients. METHODS: We reviewed the medical records of 18 patients diagnosed as MGwNM at our institute between January 2006 and December 2012. Macroscopic total resection was performed in 11 patients (61%). We evaluated the methylation status of O(6)-methylguanine-DNA methyltransferase (MGMT) and expression of isocitrate dehydrogenase 1 (IDH-1) in all cases, and deletions of 1p and 19q in available cases. RESULTS: The estimated median overall survival was 21.2 months. The median progression-free survival was 6.3 months. Six patients (33%) had MGMT methylation but IDH1 mutation was found in only one patient (6%). Gene analysis for 1p19q performed in nine patients revealed no deletion in six, 19q deletion only in two, and 1p deletion only in one. The extent of resection was significantly correlated with progression free survival on both univariate analysis and multivariate analysis (p=0.002 and p=0.013, respectively). CONCLUSION: In this study, the overall survival of MGwNM was not superior to glioblastoma. The extent of resection has a significant prognostic impact on progression-free survival. Further studies of the prognostic factors related to chemo-radio therapy, similar to studies with glioblastoma, are mandatory to improve survival. The Korean Neurosurgical Society 2016-01 2016-01-20 /pmc/articles/PMC4754586/ /pubmed/26885285 http://dx.doi.org/10.3340/jkns.2016.59.1.44 Text en Copyright © 2016 The Korean Neurosurgical Society http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Article
Kim, Hong Rye
Lee, Jae Jun
Lee, Jung-Il
Nam, Do Hyun
Suh, Yeon-Lim
Seol, Ho Jun
Malignant Glioma with Neuronal Marker Expression : A Clinicopathological Study of 18 Cases
title Malignant Glioma with Neuronal Marker Expression : A Clinicopathological Study of 18 Cases
title_full Malignant Glioma with Neuronal Marker Expression : A Clinicopathological Study of 18 Cases
title_fullStr Malignant Glioma with Neuronal Marker Expression : A Clinicopathological Study of 18 Cases
title_full_unstemmed Malignant Glioma with Neuronal Marker Expression : A Clinicopathological Study of 18 Cases
title_short Malignant Glioma with Neuronal Marker Expression : A Clinicopathological Study of 18 Cases
title_sort malignant glioma with neuronal marker expression : a clinicopathological study of 18 cases
topic Clinical Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754586/
https://www.ncbi.nlm.nih.gov/pubmed/26885285
http://dx.doi.org/10.3340/jkns.2016.59.1.44
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