Cargando…

LGG-07. IS BRAF ALTERATION OR A HISTOLOGIC ‘QUALIFIER’ A PREDICTOR OF OUTCOME IN PEDIATRIC PILOCYTIC ASTROCYTOMA?

INTRODUCTION: Pediatric pilocytic astrocytomas (PA) are the most common pediatric central nervous system tumor. Surgical resection is the primary treatment for PA with five-year survival rates up to 95%. Despite a favorable prognosis, our understanding about the prognostic value of histopathological...

Descripción completa

Detalles Bibliográficos
Autores principales: Cler, Samuel J, Skidmore, Alexander, Yahanda, Alexander T, Mian, Ali, Mackey, Kimberly, Dahiya, Sonika, Strahle, Jennifer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8168219/
http://dx.doi.org/10.1093/neuonc/noab090.131
_version_ 1783701846120988672
author Cler, Samuel J
Skidmore, Alexander
Yahanda, Alexander T
Mian, Ali
Mackey, Kimberly
Dahiya, Sonika
Strahle, Jennifer
author_facet Cler, Samuel J
Skidmore, Alexander
Yahanda, Alexander T
Mian, Ali
Mackey, Kimberly
Dahiya, Sonika
Strahle, Jennifer
author_sort Cler, Samuel J
collection PubMed
description INTRODUCTION: Pediatric pilocytic astrocytomas (PA) are the most common pediatric central nervous system tumor. Surgical resection is the primary treatment for PA with five-year survival rates up to 95%. Despite a favorable prognosis, our understanding about the prognostic value of histopathological findings, such as histopathologic qualifier* or BRAF alterations is evolving. METHODS: Patients treated for a WHO grade 1 PA at Washington University in St. Louis/St. Louis Children’s Hospital were analyzed for clinical details, including pathology diagnosis (*histopathologic qualifier refers to designations in the diagnosis such as “WHO Grade I pilocytic astrocytoma with increased proliferative index”). BRAF alterations include gene fusions and point mutations. RESULTS: 224 patients were analyzed (51% female, mean age 9.6 years). Tumors were located in the cerebellum/fourth ventricle (50%), optic pathway/hypothalamus (15%), brainstem (12%), and cerebral cortex (11%). BRAF alterations were identified in 55/77 patients (71.4%) and additional histopathologic qualifiers were present in 27/220 patients (12.3%). 196 patients (87.5%) underwent surgical treatment and 22 (9.8%) had biopsy alone. 45 patients (22%) displayed tumor progression or recurrence after resection. The presence of a histopathologic ‘qualifier’ in the topline or BRAF alteration was not associated with tumor progression or recurrence (p=0.36, p=0.77). Ki-67 proliferative indices were not predictive of progression or recurrence (p=0.94), including when controlling for extent of resection and adjuvant therapy. BRAF alterations, specifically KIAA1549 fusions, were associated with cerebellar/fourth ventricular tumor location (p<0.001) and younger patient age (p=0.03). Extent of resection was the only predictor of outcome identified in this study; patients with gross total resection had significantly lower rates of progression and recurrence (p<0.0001). CONCLUSION: BRAF alterations and histopathologic qualifiers were not associated with tumor progression or recurrence in pediatric PA, although BRAF fusions were more common in tumors located in the cerebellum/fourth ventricle and in younger patients.
format Online
Article
Text
id pubmed-8168219
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-81682192021-06-02 LGG-07. IS BRAF ALTERATION OR A HISTOLOGIC ‘QUALIFIER’ A PREDICTOR OF OUTCOME IN PEDIATRIC PILOCYTIC ASTROCYTOMA? Cler, Samuel J Skidmore, Alexander Yahanda, Alexander T Mian, Ali Mackey, Kimberly Dahiya, Sonika Strahle, Jennifer Neuro Oncol Low Grade Gliomas INTRODUCTION: Pediatric pilocytic astrocytomas (PA) are the most common pediatric central nervous system tumor. Surgical resection is the primary treatment for PA with five-year survival rates up to 95%. Despite a favorable prognosis, our understanding about the prognostic value of histopathological findings, such as histopathologic qualifier* or BRAF alterations is evolving. METHODS: Patients treated for a WHO grade 1 PA at Washington University in St. Louis/St. Louis Children’s Hospital were analyzed for clinical details, including pathology diagnosis (*histopathologic qualifier refers to designations in the diagnosis such as “WHO Grade I pilocytic astrocytoma with increased proliferative index”). BRAF alterations include gene fusions and point mutations. RESULTS: 224 patients were analyzed (51% female, mean age 9.6 years). Tumors were located in the cerebellum/fourth ventricle (50%), optic pathway/hypothalamus (15%), brainstem (12%), and cerebral cortex (11%). BRAF alterations were identified in 55/77 patients (71.4%) and additional histopathologic qualifiers were present in 27/220 patients (12.3%). 196 patients (87.5%) underwent surgical treatment and 22 (9.8%) had biopsy alone. 45 patients (22%) displayed tumor progression or recurrence after resection. The presence of a histopathologic ‘qualifier’ in the topline or BRAF alteration was not associated with tumor progression or recurrence (p=0.36, p=0.77). Ki-67 proliferative indices were not predictive of progression or recurrence (p=0.94), including when controlling for extent of resection and adjuvant therapy. BRAF alterations, specifically KIAA1549 fusions, were associated with cerebellar/fourth ventricular tumor location (p<0.001) and younger patient age (p=0.03). Extent of resection was the only predictor of outcome identified in this study; patients with gross total resection had significantly lower rates of progression and recurrence (p<0.0001). CONCLUSION: BRAF alterations and histopathologic qualifiers were not associated with tumor progression or recurrence in pediatric PA, although BRAF fusions were more common in tumors located in the cerebellum/fourth ventricle and in younger patients. Oxford University Press 2021-06-01 /pmc/articles/PMC8168219/ http://dx.doi.org/10.1093/neuonc/noab090.131 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com. https://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 (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Low Grade Gliomas
Cler, Samuel J
Skidmore, Alexander
Yahanda, Alexander T
Mian, Ali
Mackey, Kimberly
Dahiya, Sonika
Strahle, Jennifer
LGG-07. IS BRAF ALTERATION OR A HISTOLOGIC ‘QUALIFIER’ A PREDICTOR OF OUTCOME IN PEDIATRIC PILOCYTIC ASTROCYTOMA?
title LGG-07. IS BRAF ALTERATION OR A HISTOLOGIC ‘QUALIFIER’ A PREDICTOR OF OUTCOME IN PEDIATRIC PILOCYTIC ASTROCYTOMA?
title_full LGG-07. IS BRAF ALTERATION OR A HISTOLOGIC ‘QUALIFIER’ A PREDICTOR OF OUTCOME IN PEDIATRIC PILOCYTIC ASTROCYTOMA?
title_fullStr LGG-07. IS BRAF ALTERATION OR A HISTOLOGIC ‘QUALIFIER’ A PREDICTOR OF OUTCOME IN PEDIATRIC PILOCYTIC ASTROCYTOMA?
title_full_unstemmed LGG-07. IS BRAF ALTERATION OR A HISTOLOGIC ‘QUALIFIER’ A PREDICTOR OF OUTCOME IN PEDIATRIC PILOCYTIC ASTROCYTOMA?
title_short LGG-07. IS BRAF ALTERATION OR A HISTOLOGIC ‘QUALIFIER’ A PREDICTOR OF OUTCOME IN PEDIATRIC PILOCYTIC ASTROCYTOMA?
title_sort lgg-07. is braf alteration or a histologic ‘qualifier’ a predictor of outcome in pediatric pilocytic astrocytoma?
topic Low Grade Gliomas
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8168219/
http://dx.doi.org/10.1093/neuonc/noab090.131
work_keys_str_mv AT clersamuelj lgg07isbrafalterationorahistologicqualifierapredictorofoutcomeinpediatricpilocyticastrocytoma
AT skidmorealexander lgg07isbrafalterationorahistologicqualifierapredictorofoutcomeinpediatricpilocyticastrocytoma
AT yahandaalexandert lgg07isbrafalterationorahistologicqualifierapredictorofoutcomeinpediatricpilocyticastrocytoma
AT mianali lgg07isbrafalterationorahistologicqualifierapredictorofoutcomeinpediatricpilocyticastrocytoma
AT mackeykimberly lgg07isbrafalterationorahistologicqualifierapredictorofoutcomeinpediatricpilocyticastrocytoma
AT dahiyasonika lgg07isbrafalterationorahistologicqualifierapredictorofoutcomeinpediatricpilocyticastrocytoma
AT strahlejennifer lgg07isbrafalterationorahistologicqualifierapredictorofoutcomeinpediatricpilocyticastrocytoma