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MEDB-54. Standard Risk Medulloblastoma treated solely with surgery and chemo-radiation
INTRODUCTION: Medulloblastoma is the most common malignant brain tumor in children, with 5-year overall survival (OS) ranging from 60%-95% depending on subgroup and risk status. The POG 8631/CCG 923 trial (accrual 1986-1990) found a 63% 5 year OS for patients with local disease after gross total res...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9165320/ http://dx.doi.org/10.1093/neuonc/noac079.428 |
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author | Cantor, Evan Meyer, Ashley Ogle, Andrea McHugh, Michele Beck, Mary Green, Tammy Ramachandran, Lakshmi Dahiya, Sonika Cluster, Andrew Brossier, Nicole M Abdelbaki, Mohamed S Limbrick, David Perkins, Stephanie Shatara, Margaret |
author_facet | Cantor, Evan Meyer, Ashley Ogle, Andrea McHugh, Michele Beck, Mary Green, Tammy Ramachandran, Lakshmi Dahiya, Sonika Cluster, Andrew Brossier, Nicole M Abdelbaki, Mohamed S Limbrick, David Perkins, Stephanie Shatara, Margaret |
author_sort | Cantor, Evan |
collection | PubMed |
description | INTRODUCTION: Medulloblastoma is the most common malignant brain tumor in children, with 5-year overall survival (OS) ranging from 60%-95% depending on subgroup and risk status. The POG 8631/CCG 923 trial (accrual 1986-1990) found a 63% 5 year OS for patients with local disease after gross total resection treated with radiation at a dose of 23.4 Gy craniospinal radiation and posterior fossa boost to 54 Gy, vs. 80.5% 5-year OS for patients treated as per full ACNS0331 therapy including maintenance chemotherapy. Herein, we describe a long-term survival with standard-risk medulloblastoma who only received surgical resection and radiation therapy. CASE: A 17-year-old male presented with acute onset of hypertension, bradycardia, headache, and blurry vision and was found to have a heterogeneously enhancing posterior fossa mass with mass effect on the fourth ventricle and hydrocephalus on brain MRI. He underwent gross total resection of the tumor and histopathology revealed medulloblastoma with classic and large cell features. Fluorescence in situ hybridization (FISH) was negative for MYC, MYCN amplification, or HER2 gain. Cerebrospinal fluid cytology was negative for neoplastic cells, and spinal MRI did not reveal any drop metastases. The patient initiated therapy per ACNS0331 with craniospinal irradiation posterior fossa boost. He also received weekly vincristine. After completion of radiation therapy, the family declined further chemotherapy despite medical advice. He had no evidence of relapse most recently at 51 months from completion of therapy. Next generation sequencing and methylation testing are currently pending. CONCLUSION: Current efforts aim at optimizing therapy based on molecular subgrouping, to minimize long-term adverse events associated with current therapies. We report a unique case of an adolescent male with an standard-risk medulloblastoma, who achieved remission with only radiotherapy. Further molecular tumor analysis may elucidate the response of the tumor. |
format | Online Article Text |
id | pubmed-9165320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-91653202022-06-06 MEDB-54. Standard Risk Medulloblastoma treated solely with surgery and chemo-radiation Cantor, Evan Meyer, Ashley Ogle, Andrea McHugh, Michele Beck, Mary Green, Tammy Ramachandran, Lakshmi Dahiya, Sonika Cluster, Andrew Brossier, Nicole M Abdelbaki, Mohamed S Limbrick, David Perkins, Stephanie Shatara, Margaret Neuro Oncol Medulloblastoma INTRODUCTION: Medulloblastoma is the most common malignant brain tumor in children, with 5-year overall survival (OS) ranging from 60%-95% depending on subgroup and risk status. The POG 8631/CCG 923 trial (accrual 1986-1990) found a 63% 5 year OS for patients with local disease after gross total resection treated with radiation at a dose of 23.4 Gy craniospinal radiation and posterior fossa boost to 54 Gy, vs. 80.5% 5-year OS for patients treated as per full ACNS0331 therapy including maintenance chemotherapy. Herein, we describe a long-term survival with standard-risk medulloblastoma who only received surgical resection and radiation therapy. CASE: A 17-year-old male presented with acute onset of hypertension, bradycardia, headache, and blurry vision and was found to have a heterogeneously enhancing posterior fossa mass with mass effect on the fourth ventricle and hydrocephalus on brain MRI. He underwent gross total resection of the tumor and histopathology revealed medulloblastoma with classic and large cell features. Fluorescence in situ hybridization (FISH) was negative for MYC, MYCN amplification, or HER2 gain. Cerebrospinal fluid cytology was negative for neoplastic cells, and spinal MRI did not reveal any drop metastases. The patient initiated therapy per ACNS0331 with craniospinal irradiation posterior fossa boost. He also received weekly vincristine. After completion of radiation therapy, the family declined further chemotherapy despite medical advice. He had no evidence of relapse most recently at 51 months from completion of therapy. Next generation sequencing and methylation testing are currently pending. CONCLUSION: Current efforts aim at optimizing therapy based on molecular subgrouping, to minimize long-term adverse events associated with current therapies. We report a unique case of an adolescent male with an standard-risk medulloblastoma, who achieved remission with only radiotherapy. Further molecular tumor analysis may elucidate the response of the tumor. Oxford University Press 2022-06-03 /pmc/articles/PMC9165320/ http://dx.doi.org/10.1093/neuonc/noac079.428 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (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 | Medulloblastoma Cantor, Evan Meyer, Ashley Ogle, Andrea McHugh, Michele Beck, Mary Green, Tammy Ramachandran, Lakshmi Dahiya, Sonika Cluster, Andrew Brossier, Nicole M Abdelbaki, Mohamed S Limbrick, David Perkins, Stephanie Shatara, Margaret MEDB-54. Standard Risk Medulloblastoma treated solely with surgery and chemo-radiation |
title | MEDB-54. Standard Risk Medulloblastoma treated solely with surgery and chemo-radiation |
title_full | MEDB-54. Standard Risk Medulloblastoma treated solely with surgery and chemo-radiation |
title_fullStr | MEDB-54. Standard Risk Medulloblastoma treated solely with surgery and chemo-radiation |
title_full_unstemmed | MEDB-54. Standard Risk Medulloblastoma treated solely with surgery and chemo-radiation |
title_short | MEDB-54. Standard Risk Medulloblastoma treated solely with surgery and chemo-radiation |
title_sort | medb-54. standard risk medulloblastoma treated solely with surgery and chemo-radiation |
topic | Medulloblastoma |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9165320/ http://dx.doi.org/10.1093/neuonc/noac079.428 |
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