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HGG-42. CLINICAL FEATURES AND TREATMENT OUTCOME OF MALIGNANT GLIOMAS IN CHILDREN AND ADOLESCENTS
INTRODUCTION: Malignant gliomas in children and adolescents are rare. They are difficult to treat and are associated with an extremely poor prognosis. SUBJECTS AND METHODS: The treatment and outcomes of WHO grade IV -gliomas and diffuse intrinsic pontine gliomas (DIPG) in children and adolescents (A...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7715910/ http://dx.doi.org/10.1093/neuonc/noaa222.323 |
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author | Yonezawa, Hajime Uchida, Hiroyuki Higa, Nayuta Oyoshi, Tatsuki Yoshimoto, Koji |
author_facet | Yonezawa, Hajime Uchida, Hiroyuki Higa, Nayuta Oyoshi, Tatsuki Yoshimoto, Koji |
author_sort | Yonezawa, Hajime |
collection | PubMed |
description | INTRODUCTION: Malignant gliomas in children and adolescents are rare. They are difficult to treat and are associated with an extremely poor prognosis. SUBJECTS AND METHODS: The treatment and outcomes of WHO grade IV -gliomas and diffuse intrinsic pontine gliomas (DIPG) in children and adolescents (Age 4–39, median 28) treated at our institute since 2001 were retrospectively reviewed. Thirty-five cases were included in this study. Nine cases were located in their brain stem and 2 of them were diagnosed as DIPG clinically without biopsy. Three (brain stem -2, thalamus- 1) cases were diffuse midline glioma H3 K27 M mutant. Remaining 30 cases were diagnosed histologically as glioblastoma. Expect for 2 cases, all were irradiated. Twenty-four cases were treated with temozolomide (TMZ). Bevacizumab (BEV) was administrated as an initial therapy in 10 cases (concomitant with TMZ in 9 cases) and was administrated at the time of relapse in 9 cases. In summary, 19 cases were treated with BEV. RESULTS: Median survival time (MST) of all cases was 16.8 (4.4 -152.3) months. In total, BEV did not prolonged overall survival (OS), MST 16.02 vs 14.44, (p=0.498). Among adolescents (age 15–39), patients treated with BEV had a trend of longer OS but did not reached statistical significance, MST 19.64 vs 10.76 (p=0.167). An extent of resection and KPS =>70 at discharge from hospital were beneficial factors associated with prolonged OS. CONCLUSION: As well as in elderly cases, multidisciplinary treatment including resection, radiation and chemotherapy including BEV improves outcomes. |
format | Online Article Text |
id | pubmed-7715910 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-77159102020-12-09 HGG-42. CLINICAL FEATURES AND TREATMENT OUTCOME OF MALIGNANT GLIOMAS IN CHILDREN AND ADOLESCENTS Yonezawa, Hajime Uchida, Hiroyuki Higa, Nayuta Oyoshi, Tatsuki Yoshimoto, Koji Neuro Oncol High Grade Glioma INTRODUCTION: Malignant gliomas in children and adolescents are rare. They are difficult to treat and are associated with an extremely poor prognosis. SUBJECTS AND METHODS: The treatment and outcomes of WHO grade IV -gliomas and diffuse intrinsic pontine gliomas (DIPG) in children and adolescents (Age 4–39, median 28) treated at our institute since 2001 were retrospectively reviewed. Thirty-five cases were included in this study. Nine cases were located in their brain stem and 2 of them were diagnosed as DIPG clinically without biopsy. Three (brain stem -2, thalamus- 1) cases were diffuse midline glioma H3 K27 M mutant. Remaining 30 cases were diagnosed histologically as glioblastoma. Expect for 2 cases, all were irradiated. Twenty-four cases were treated with temozolomide (TMZ). Bevacizumab (BEV) was administrated as an initial therapy in 10 cases (concomitant with TMZ in 9 cases) and was administrated at the time of relapse in 9 cases. In summary, 19 cases were treated with BEV. RESULTS: Median survival time (MST) of all cases was 16.8 (4.4 -152.3) months. In total, BEV did not prolonged overall survival (OS), MST 16.02 vs 14.44, (p=0.498). Among adolescents (age 15–39), patients treated with BEV had a trend of longer OS but did not reached statistical significance, MST 19.64 vs 10.76 (p=0.167). An extent of resection and KPS =>70 at discharge from hospital were beneficial factors associated with prolonged OS. CONCLUSION: As well as in elderly cases, multidisciplinary treatment including resection, radiation and chemotherapy including BEV improves outcomes. Oxford University Press 2020-12-04 /pmc/articles/PMC7715910/ http://dx.doi.org/10.1093/neuonc/noaa222.323 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. 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 (http://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 | High Grade Glioma Yonezawa, Hajime Uchida, Hiroyuki Higa, Nayuta Oyoshi, Tatsuki Yoshimoto, Koji HGG-42. CLINICAL FEATURES AND TREATMENT OUTCOME OF MALIGNANT GLIOMAS IN CHILDREN AND ADOLESCENTS |
title | HGG-42. CLINICAL FEATURES AND TREATMENT OUTCOME OF MALIGNANT GLIOMAS IN CHILDREN AND ADOLESCENTS |
title_full | HGG-42. CLINICAL FEATURES AND TREATMENT OUTCOME OF MALIGNANT GLIOMAS IN CHILDREN AND ADOLESCENTS |
title_fullStr | HGG-42. CLINICAL FEATURES AND TREATMENT OUTCOME OF MALIGNANT GLIOMAS IN CHILDREN AND ADOLESCENTS |
title_full_unstemmed | HGG-42. CLINICAL FEATURES AND TREATMENT OUTCOME OF MALIGNANT GLIOMAS IN CHILDREN AND ADOLESCENTS |
title_short | HGG-42. CLINICAL FEATURES AND TREATMENT OUTCOME OF MALIGNANT GLIOMAS IN CHILDREN AND ADOLESCENTS |
title_sort | hgg-42. clinical features and treatment outcome of malignant gliomas in children and adolescents |
topic | High Grade Glioma |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7715910/ http://dx.doi.org/10.1093/neuonc/noaa222.323 |
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