Clinicopathological characteristics and survival of spinal cord astrocytomas

Abstract Background Due to their rarity, the clinicopathological characteristics and prognostic factors of spinal cord gliomas are still unclear. Here, we aimed to clarify these issues in a cohort of 108 spinal cord astrocytomas. Methods We characterized the clinicopathological characteristics, incl...

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Main Authors: Yao‐Wu Zhang, Rui‐Chao Chai, Ren Cao, Wen‐Ju Jiang, Wei‐Hao Liu, Yu‐Lun Xu, Jun Yang, Yong‐Zhi Wang, Wen‐Qing Jia
Format: Article
Language:English
Published: Wiley 2020-10-01
Series:Cancer Medicine
Subjects:
Online Access:https://doi.org/10.1002/cam4.3364
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author Yao‐Wu Zhang
Rui‐Chao Chai
Ren Cao
Wen‐Ju Jiang
Wei‐Hao Liu
Yu‐Lun Xu
Jun Yang
Yong‐Zhi Wang
Wen‐Qing Jia
author_facet Yao‐Wu Zhang
Rui‐Chao Chai
Ren Cao
Wen‐Ju Jiang
Wei‐Hao Liu
Yu‐Lun Xu
Jun Yang
Yong‐Zhi Wang
Wen‐Qing Jia
author_sort Yao‐Wu Zhang
collection DOAJ
description Abstract Background Due to their rarity, the clinicopathological characteristics and prognostic factors of spinal cord gliomas are still unclear. Here, we aimed to clarify these issues in a cohort of 108 spinal cord astrocytomas. Methods We characterized the clinicopathological characteristics, including 2016 World Health Organization (WHO) grade, age, sex, location, segment length, resection, pre‐ and postsurgery, Modified McCormick Scale (MMS), radio‐ and chemotherapy, and Ki‐67 and H3 K27M mutations, in 108 spinal cord astrocytomas through heatmaps. The Cox regression analysis and Kaplan‐Meier curves were used to study the prognostic value of these clinicopathological features. Results There are a total 38 H3 K27M‐mutant tumors, including 31 cases with histological grade II/III tumors. The age of low‐grade astrocytoma patients (WHO grade I/II, n = 54) was significantly younger (27.0 vs 35.5 years, P = .001) than those with high‐grade tumors (WHO grade III/IV, n = 54). All patients underwent surgical resection with neurophysiological monitoring, and the surgery did not result in significant changes in MMS. The presurgery MMS was associated with overall survival in the high‐grade subgroup (P = .008) but not in the low‐grade subgroup (P = .312). While, the high content of resection improved the survival of only patients with low‐grade astrocytomas (P = .016) but not those with high‐grade astrocytomas (P = .475). Both the low‐grade and high‐grade astrocytomas had no obvious benefit from neither adjuvant chemotherapy nor radiotherapy (all P > .05). Conclusions We characterized the clinicopathological characteristics and their prognostic values in 108 spinal cord astrocytomas, which could help with evidence‐based management of spinal cord astrocytomas.
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spelling doaj.art-041549128ed246a3a5d9e1e6b07a83db2023-04-25T14:00:49ZengWileyCancer Medicine2045-76342020-10-019196996700610.1002/cam4.3364Clinicopathological characteristics and survival of spinal cord astrocytomasYao‐Wu Zhang0Rui‐Chao Chai1Ren Cao2Wen‐Ju Jiang3Wei‐Hao Liu4Yu‐Lun Xu5Jun Yang6Yong‐Zhi Wang7Wen‐Qing Jia8Department of Neurosurgery Beijing Tiantan Hospital, Capital Medical University Beijing ChinaChina National Clinical Research Center for Neurological Diseases Beijing ChinaDepartment of Neurosurgery Beijing Tiantan Hospital, Capital Medical University Beijing ChinaDepartment of Neurosurgery Beijing Tiantan Hospital, Capital Medical University Beijing ChinaDepartment of Neurosurgery Beijing Tiantan Hospital, Capital Medical University Beijing ChinaDepartment of Neurosurgery Beijing Tiantan Hospital, Capital Medical University Beijing ChinaDepartment of Neurosurgery Beijing Tiantan Hospital, Capital Medical University Beijing ChinaDepartment of Neurosurgery Beijing Tiantan Hospital, Capital Medical University Beijing ChinaDepartment of Neurosurgery Beijing Tiantan Hospital, Capital Medical University Beijing ChinaAbstract Background Due to their rarity, the clinicopathological characteristics and prognostic factors of spinal cord gliomas are still unclear. Here, we aimed to clarify these issues in a cohort of 108 spinal cord astrocytomas. Methods We characterized the clinicopathological characteristics, including 2016 World Health Organization (WHO) grade, age, sex, location, segment length, resection, pre‐ and postsurgery, Modified McCormick Scale (MMS), radio‐ and chemotherapy, and Ki‐67 and H3 K27M mutations, in 108 spinal cord astrocytomas through heatmaps. The Cox regression analysis and Kaplan‐Meier curves were used to study the prognostic value of these clinicopathological features. Results There are a total 38 H3 K27M‐mutant tumors, including 31 cases with histological grade II/III tumors. The age of low‐grade astrocytoma patients (WHO grade I/II, n = 54) was significantly younger (27.0 vs 35.5 years, P = .001) than those with high‐grade tumors (WHO grade III/IV, n = 54). All patients underwent surgical resection with neurophysiological monitoring, and the surgery did not result in significant changes in MMS. The presurgery MMS was associated with overall survival in the high‐grade subgroup (P = .008) but not in the low‐grade subgroup (P = .312). While, the high content of resection improved the survival of only patients with low‐grade astrocytomas (P = .016) but not those with high‐grade astrocytomas (P = .475). Both the low‐grade and high‐grade astrocytomas had no obvious benefit from neither adjuvant chemotherapy nor radiotherapy (all P > .05). Conclusions We characterized the clinicopathological characteristics and their prognostic values in 108 spinal cord astrocytomas, which could help with evidence‐based management of spinal cord astrocytomas.https://doi.org/10.1002/cam4.3364astrocytomaclinicopathological featureH3 K27Mspinal cord tumorsurvival
spellingShingle Yao‐Wu Zhang
Rui‐Chao Chai
Ren Cao
Wen‐Ju Jiang
Wei‐Hao Liu
Yu‐Lun Xu
Jun Yang
Yong‐Zhi Wang
Wen‐Qing Jia
Clinicopathological characteristics and survival of spinal cord astrocytomas
Cancer Medicine
astrocytoma
clinicopathological feature
H3 K27M
spinal cord tumor
survival
title Clinicopathological characteristics and survival of spinal cord astrocytomas
title_full Clinicopathological characteristics and survival of spinal cord astrocytomas
title_fullStr Clinicopathological characteristics and survival of spinal cord astrocytomas
title_full_unstemmed Clinicopathological characteristics and survival of spinal cord astrocytomas
title_short Clinicopathological characteristics and survival of spinal cord astrocytomas
title_sort clinicopathological characteristics and survival of spinal cord astrocytomas
topic astrocytoma
clinicopathological feature
H3 K27M
spinal cord tumor
survival
url https://doi.org/10.1002/cam4.3364
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