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Survival and prognostic factors in childhood medulloblastoma: A Brazilian single center experience from 1995 to 2016

BACKGROUND: Medulloblastoma is the most common malignant brain tumor in the pediatric population. Despite prognosis improvement in the past two decades, one-third of the patients still remain incurable. New evidence suggests that medulloblastoma comprises four distinct entities; therefore, treatment...

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Autores principales: Bleil, Cristina Birlem, Bizzi, Jorge Wladimir Junqueira, Bedin, Andre, de Oliveira, Francine Hehn, Antunes, Ápio Cláudio Martins
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6744760/
https://www.ncbi.nlm.nih.gov/pubmed/31528456
http://dx.doi.org/10.25259/SNI-237-2019
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author Bleil, Cristina Birlem
Bizzi, Jorge Wladimir Junqueira
Bedin, Andre
de Oliveira, Francine Hehn
Antunes, Ápio Cláudio Martins
author_facet Bleil, Cristina Birlem
Bizzi, Jorge Wladimir Junqueira
Bedin, Andre
de Oliveira, Francine Hehn
Antunes, Ápio Cláudio Martins
author_sort Bleil, Cristina Birlem
collection PubMed
description BACKGROUND: Medulloblastoma is the most common malignant brain tumor in the pediatric population. Despite prognosis improvement in the past two decades, one-third of the patients still remain incurable. New evidence suggests that medulloblastoma comprises four distinct entities; therefore, treatment de-escalation is required. The aim of this article is to evaluate epidemiological data from patients treated at our institution. The primary objective is to analyze overall survival (OS) and event-free survival (EFS) and the secondary objective is to identify prognostic factor from this cohort. METHODS: We retrospectively analyzed 69 patients who underwent surgical resection for medulloblastoma among 423 children from the tumor registry data bank of Santo Antônio Children’s Hospital from 1995 to 2016. Kaplan–Meier method and Cox regression analysis were used to identify OS, EFS, and prognostic factors. RESULTS: The 5-year OS and EFS rates found were 44.5% and 36.4%, respectively. The extent of resection and radiotherapy as adjuvant treatments was positively correlated to outcome while metastatic disease at diagnosis was negatively related to OS. Age younger than 3 years old did not have a worse outcome in our cohort. CONCLUSION: Similar results to population-based studies were found, but we still face difficulties due to living in a developing country. In the near future, we look forward to new diagnostic techniques that will enable us to classify medulloblastomas according to molecular subgroups.
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spelling pubmed-67447602019-09-16 Survival and prognostic factors in childhood medulloblastoma: A Brazilian single center experience from 1995 to 2016 Bleil, Cristina Birlem Bizzi, Jorge Wladimir Junqueira Bedin, Andre de Oliveira, Francine Hehn Antunes, Ápio Cláudio Martins Surg Neurol Int Original Article BACKGROUND: Medulloblastoma is the most common malignant brain tumor in the pediatric population. Despite prognosis improvement in the past two decades, one-third of the patients still remain incurable. New evidence suggests that medulloblastoma comprises four distinct entities; therefore, treatment de-escalation is required. The aim of this article is to evaluate epidemiological data from patients treated at our institution. The primary objective is to analyze overall survival (OS) and event-free survival (EFS) and the secondary objective is to identify prognostic factor from this cohort. METHODS: We retrospectively analyzed 69 patients who underwent surgical resection for medulloblastoma among 423 children from the tumor registry data bank of Santo Antônio Children’s Hospital from 1995 to 2016. Kaplan–Meier method and Cox regression analysis were used to identify OS, EFS, and prognostic factors. RESULTS: The 5-year OS and EFS rates found were 44.5% and 36.4%, respectively. The extent of resection and radiotherapy as adjuvant treatments was positively correlated to outcome while metastatic disease at diagnosis was negatively related to OS. Age younger than 3 years old did not have a worse outcome in our cohort. CONCLUSION: Similar results to population-based studies were found, but we still face difficulties due to living in a developing country. In the near future, we look forward to new diagnostic techniques that will enable us to classify medulloblastomas according to molecular subgroups. Scientific Scholar 2019-06-25 /pmc/articles/PMC6744760/ /pubmed/31528456 http://dx.doi.org/10.25259/SNI-237-2019 Text en Copyright: © 2019 Surgical Neurology International http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Bleil, Cristina Birlem
Bizzi, Jorge Wladimir Junqueira
Bedin, Andre
de Oliveira, Francine Hehn
Antunes, Ápio Cláudio Martins
Survival and prognostic factors in childhood medulloblastoma: A Brazilian single center experience from 1995 to 2016
title Survival and prognostic factors in childhood medulloblastoma: A Brazilian single center experience from 1995 to 2016
title_full Survival and prognostic factors in childhood medulloblastoma: A Brazilian single center experience from 1995 to 2016
title_fullStr Survival and prognostic factors in childhood medulloblastoma: A Brazilian single center experience from 1995 to 2016
title_full_unstemmed Survival and prognostic factors in childhood medulloblastoma: A Brazilian single center experience from 1995 to 2016
title_short Survival and prognostic factors in childhood medulloblastoma: A Brazilian single center experience from 1995 to 2016
title_sort survival and prognostic factors in childhood medulloblastoma: a brazilian single center experience from 1995 to 2016
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6744760/
https://www.ncbi.nlm.nih.gov/pubmed/31528456
http://dx.doi.org/10.25259/SNI-237-2019
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