Cargando…

Surgical treatment and prognosis of focal brainstem gliomas in children: A 7 year single center experience

This study aims to describe the role of open surgical treatment for focal brainstem gliomas (FBSGs) with the assistance of multimodal neuronavigation and intraoperative neurophysiological monitoring (IOM) in children to investigate the efficacy of microsurgical treatment in pediatric FBSGs. Also the...

Descripción completa

Detalles Bibliográficos
Autores principales: Sun, Tao, Xu, Yan, Pan, Changcun, Liu, Yuhan, Tian, Yongji, Li, Chunde, Di, Fei, Zhang, Liwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478697/
https://www.ncbi.nlm.nih.gov/pubmed/32899058
http://dx.doi.org/10.1097/MD.0000000000022029
_version_ 1783580110870282240
author Sun, Tao
Xu, Yan
Pan, Changcun
Liu, Yuhan
Tian, Yongji
Li, Chunde
Di, Fei
Zhang, Liwei
author_facet Sun, Tao
Xu, Yan
Pan, Changcun
Liu, Yuhan
Tian, Yongji
Li, Chunde
Di, Fei
Zhang, Liwei
author_sort Sun, Tao
collection PubMed
description This study aims to describe the role of open surgical treatment for focal brainstem gliomas (FBSGs) with the assistance of multimodal neuronavigation and intraoperative neurophysiological monitoring (IOM) in children to investigate the efficacy of microsurgical treatment in pediatric FBSGs. Also the prognostic factors related to the overall survival (OS) of FBSGs to describe the patient and tumor characteristics relevant to prognosis/outcome were focused on. Clinical data of 63 pediatric patients below 16 years of age with FBSGs admitted to the Neurosurgical Unit of Beijing Tiantan Hospital from January 2012 to December 2018 were retrospectively analyzed. All patients underwent initial surgical treatment, followed by magnetic resonance diffusion tensor imaging (DTI), neuronavigation and IOM. Gross or near total resection (GTR or NTR) was achieved in 57/63 (90.5%) cases, and subtotal resection (STR) was achieved in 6/63 (9.5%) cases. Postoperative adjuvant therapy was received by 27/63 (42.9%) cases. Postoperative pathological examination revealed that 36/63 (57.1%) cases had grade I gliomas, 22/63 (34.9%) had grade II, and 5/63 (8.0%) had grade III–IV gliomas according to the WHO classification. The mean Karnofsky score preoperatively was 60, and at the time of follow-up was 90. Consecutively, 6 cases demonstrated disease progression, and 5 of these were deceased. The OS in all patients was 81.2% at 5 years. Histological grade (P < .001) and age at diagnosis (P = .023) showed significant association with prolonged OS. Multimodal neuronavigation and IOM allow very precise intracranial surgery, contributing to a maximally safe resection that might decrease the postoperative disability and mortality rate. This study also showed that pediatric FBSGs were mostly low-grade tumors with excellent surgical outcomes. Consequently, it is suggested that microsurgery can be used to treat FBSGs in children in order to provide better prognosis and survival outcomes.
format Online
Article
Text
id pubmed-7478697
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Lippincott Williams & Wilkins
record_format MEDLINE/PubMed
spelling pubmed-74786972020-09-24 Surgical treatment and prognosis of focal brainstem gliomas in children: A 7 year single center experience Sun, Tao Xu, Yan Pan, Changcun Liu, Yuhan Tian, Yongji Li, Chunde Di, Fei Zhang, Liwei Medicine (Baltimore) 5300 This study aims to describe the role of open surgical treatment for focal brainstem gliomas (FBSGs) with the assistance of multimodal neuronavigation and intraoperative neurophysiological monitoring (IOM) in children to investigate the efficacy of microsurgical treatment in pediatric FBSGs. Also the prognostic factors related to the overall survival (OS) of FBSGs to describe the patient and tumor characteristics relevant to prognosis/outcome were focused on. Clinical data of 63 pediatric patients below 16 years of age with FBSGs admitted to the Neurosurgical Unit of Beijing Tiantan Hospital from January 2012 to December 2018 were retrospectively analyzed. All patients underwent initial surgical treatment, followed by magnetic resonance diffusion tensor imaging (DTI), neuronavigation and IOM. Gross or near total resection (GTR or NTR) was achieved in 57/63 (90.5%) cases, and subtotal resection (STR) was achieved in 6/63 (9.5%) cases. Postoperative adjuvant therapy was received by 27/63 (42.9%) cases. Postoperative pathological examination revealed that 36/63 (57.1%) cases had grade I gliomas, 22/63 (34.9%) had grade II, and 5/63 (8.0%) had grade III–IV gliomas according to the WHO classification. The mean Karnofsky score preoperatively was 60, and at the time of follow-up was 90. Consecutively, 6 cases demonstrated disease progression, and 5 of these were deceased. The OS in all patients was 81.2% at 5 years. Histological grade (P < .001) and age at diagnosis (P = .023) showed significant association with prolonged OS. Multimodal neuronavigation and IOM allow very precise intracranial surgery, contributing to a maximally safe resection that might decrease the postoperative disability and mortality rate. This study also showed that pediatric FBSGs were mostly low-grade tumors with excellent surgical outcomes. Consequently, it is suggested that microsurgery can be used to treat FBSGs in children in order to provide better prognosis and survival outcomes. Lippincott Williams & Wilkins 2020-09-04 /pmc/articles/PMC7478697/ /pubmed/32899058 http://dx.doi.org/10.1097/MD.0000000000022029 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle 5300
Sun, Tao
Xu, Yan
Pan, Changcun
Liu, Yuhan
Tian, Yongji
Li, Chunde
Di, Fei
Zhang, Liwei
Surgical treatment and prognosis of focal brainstem gliomas in children: A 7 year single center experience
title Surgical treatment and prognosis of focal brainstem gliomas in children: A 7 year single center experience
title_full Surgical treatment and prognosis of focal brainstem gliomas in children: A 7 year single center experience
title_fullStr Surgical treatment and prognosis of focal brainstem gliomas in children: A 7 year single center experience
title_full_unstemmed Surgical treatment and prognosis of focal brainstem gliomas in children: A 7 year single center experience
title_short Surgical treatment and prognosis of focal brainstem gliomas in children: A 7 year single center experience
title_sort surgical treatment and prognosis of focal brainstem gliomas in children: a 7 year single center experience
topic 5300
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478697/
https://www.ncbi.nlm.nih.gov/pubmed/32899058
http://dx.doi.org/10.1097/MD.0000000000022029
work_keys_str_mv AT suntao surgicaltreatmentandprognosisoffocalbrainstemgliomasinchildrena7yearsinglecenterexperience
AT xuyan surgicaltreatmentandprognosisoffocalbrainstemgliomasinchildrena7yearsinglecenterexperience
AT panchangcun surgicaltreatmentandprognosisoffocalbrainstemgliomasinchildrena7yearsinglecenterexperience
AT liuyuhan surgicaltreatmentandprognosisoffocalbrainstemgliomasinchildrena7yearsinglecenterexperience
AT tianyongji surgicaltreatmentandprognosisoffocalbrainstemgliomasinchildrena7yearsinglecenterexperience
AT lichunde surgicaltreatmentandprognosisoffocalbrainstemgliomasinchildrena7yearsinglecenterexperience
AT difei surgicaltreatmentandprognosisoffocalbrainstemgliomasinchildrena7yearsinglecenterexperience
AT zhangliwei surgicaltreatmentandprognosisoffocalbrainstemgliomasinchildrena7yearsinglecenterexperience