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CLINICAL, DEMOGRAPHIC, ANATOMOPATHOLOGICAL, AND MOLECULAR FINDINGS IN PATIENTS WITH MEDULLOBLASTOMA TREATED IN A SINGLE HEALTH FACILITY
OBJECTIVE: To describe the clinical, demographic, anatomopathological, molecular, and survival characteristics of patients with medulloblastoma. METHODS: Retrospective study based on patient information obtained from the review of medical records. Overall and event-free survival were analyzed using...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade de Pediatria de São Paulo
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7669220/ https://www.ncbi.nlm.nih.gov/pubmed/33206839 http://dx.doi.org/10.1590/1984-0462/2021/39/2019298 |
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author | Hoffmann, Iva Loureiro Cardinalli, Izilda Aparecida Yunes, José Andrés Seidinger, Ana Luiza Pereira, Ricardo Mendes |
author_facet | Hoffmann, Iva Loureiro Cardinalli, Izilda Aparecida Yunes, José Andrés Seidinger, Ana Luiza Pereira, Ricardo Mendes |
author_sort | Hoffmann, Iva Loureiro |
collection | PubMed |
description | OBJECTIVE: To describe the clinical, demographic, anatomopathological, molecular, and survival characteristics of patients with medulloblastoma. METHODS: Retrospective study based on patient information obtained from the review of medical records. Overall and event-free survival were analyzed using the Kaplan-Meier estimator, and the curves were compared by the log-rank test. RESULTS: Among the patients investigated, 70 were male (66%), and age at diagnosis ranged from 2 months to 22 years. The most frequent signs and symptoms were headache (80.8%) and vomiting (75.8%). Regarding treatment, most patients (63.2%) underwent complete surgical resection, with a predominance of classic histology (63.2%). The 5-year overall survival rate was 67.9%, and the 10-year rate was 64.2%. Patients with molecular profile characteristic of the wingless (WNT) subgroup had a better prognosis, with 5-year overall survival of 75%. CONCLUSIONS: The clinical, demographic, anatomopathological, and molecular characteristics of patients with medulloblastoma described in the present study were mostly similar to those reported in the literature. Patients submitted to complete tumor resection had better clinical outcomes than those who underwent incomplete resection/biopsy. Patients classified as high-risk showed worse overall and event-free survival than those in the standard-risk group, and the presence of metastasis at diagnosis was associated with recurrence. |
format | Online Article Text |
id | pubmed-7669220 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Sociedade de Pediatria de São Paulo |
record_format | MEDLINE/PubMed |
spelling | pubmed-76692202020-11-23 CLINICAL, DEMOGRAPHIC, ANATOMOPATHOLOGICAL, AND MOLECULAR FINDINGS IN PATIENTS WITH MEDULLOBLASTOMA TREATED IN A SINGLE HEALTH FACILITY Hoffmann, Iva Loureiro Cardinalli, Izilda Aparecida Yunes, José Andrés Seidinger, Ana Luiza Pereira, Ricardo Mendes Rev Paul Pediatr Original Article OBJECTIVE: To describe the clinical, demographic, anatomopathological, molecular, and survival characteristics of patients with medulloblastoma. METHODS: Retrospective study based on patient information obtained from the review of medical records. Overall and event-free survival were analyzed using the Kaplan-Meier estimator, and the curves were compared by the log-rank test. RESULTS: Among the patients investigated, 70 were male (66%), and age at diagnosis ranged from 2 months to 22 years. The most frequent signs and symptoms were headache (80.8%) and vomiting (75.8%). Regarding treatment, most patients (63.2%) underwent complete surgical resection, with a predominance of classic histology (63.2%). The 5-year overall survival rate was 67.9%, and the 10-year rate was 64.2%. Patients with molecular profile characteristic of the wingless (WNT) subgroup had a better prognosis, with 5-year overall survival of 75%. CONCLUSIONS: The clinical, demographic, anatomopathological, and molecular characteristics of patients with medulloblastoma described in the present study were mostly similar to those reported in the literature. Patients submitted to complete tumor resection had better clinical outcomes than those who underwent incomplete resection/biopsy. Patients classified as high-risk showed worse overall and event-free survival than those in the standard-risk group, and the presence of metastasis at diagnosis was associated with recurrence. Sociedade de Pediatria de São Paulo 2020-11-16 /pmc/articles/PMC7669220/ /pubmed/33206839 http://dx.doi.org/10.1590/1984-0462/2021/39/2019298 Text en https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License |
spellingShingle | Original Article Hoffmann, Iva Loureiro Cardinalli, Izilda Aparecida Yunes, José Andrés Seidinger, Ana Luiza Pereira, Ricardo Mendes CLINICAL, DEMOGRAPHIC, ANATOMOPATHOLOGICAL, AND MOLECULAR FINDINGS IN PATIENTS WITH MEDULLOBLASTOMA TREATED IN A SINGLE HEALTH FACILITY |
title | CLINICAL, DEMOGRAPHIC, ANATOMOPATHOLOGICAL, AND MOLECULAR FINDINGS IN
PATIENTS WITH MEDULLOBLASTOMA TREATED IN A SINGLE HEALTH
FACILITY |
title_full | CLINICAL, DEMOGRAPHIC, ANATOMOPATHOLOGICAL, AND MOLECULAR FINDINGS IN
PATIENTS WITH MEDULLOBLASTOMA TREATED IN A SINGLE HEALTH
FACILITY |
title_fullStr | CLINICAL, DEMOGRAPHIC, ANATOMOPATHOLOGICAL, AND MOLECULAR FINDINGS IN
PATIENTS WITH MEDULLOBLASTOMA TREATED IN A SINGLE HEALTH
FACILITY |
title_full_unstemmed | CLINICAL, DEMOGRAPHIC, ANATOMOPATHOLOGICAL, AND MOLECULAR FINDINGS IN
PATIENTS WITH MEDULLOBLASTOMA TREATED IN A SINGLE HEALTH
FACILITY |
title_short | CLINICAL, DEMOGRAPHIC, ANATOMOPATHOLOGICAL, AND MOLECULAR FINDINGS IN
PATIENTS WITH MEDULLOBLASTOMA TREATED IN A SINGLE HEALTH
FACILITY |
title_sort | clinical, demographic, anatomopathological, and molecular findings in
patients with medulloblastoma treated in a single health
facility |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7669220/ https://www.ncbi.nlm.nih.gov/pubmed/33206839 http://dx.doi.org/10.1590/1984-0462/2021/39/2019298 |
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