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MBCL-50. DISMAL OUTCOME OF HIGH RISK MEDULLOBLASTOMA TREATED WITH CHEMOTHERAPY FIRST APPROACH IN MALAYSIA

INTRODUCTION: Patients with high risk medulloblastoma are treated either with high dose chemotherapy or hyperfractionated radiotherapy. Both approaches are not feasible in resource-limited countries. POG9031 trial has reported favourable outcome for high risk medulloblastoma using standard chemother...

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Autores principales: Quah, Shiao Wei, Rahman, E J Abdul, Ibrahim, H Mohd, Muda, Z, Othman, I S, Unni, M N Mohamed, Gunasagaran, K, Ang, M P, Goh, C B, Teh, K H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7715103/
http://dx.doi.org/10.1093/neuonc/noaa222.519
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author Quah, Shiao Wei
Rahman, E J Abdul
Ibrahim, H Mohd
Muda, Z
Othman, I S
Unni, M N Mohamed
Gunasagaran, K
Ang, M P
Goh, C B
Teh, K H
author_facet Quah, Shiao Wei
Rahman, E J Abdul
Ibrahim, H Mohd
Muda, Z
Othman, I S
Unni, M N Mohamed
Gunasagaran, K
Ang, M P
Goh, C B
Teh, K H
author_sort Quah, Shiao Wei
collection PubMed
description INTRODUCTION: Patients with high risk medulloblastoma are treated either with high dose chemotherapy or hyperfractionated radiotherapy. Both approaches are not feasible in resource-limited countries. POG9031 trial has reported favourable outcome for high risk medulloblastoma using standard chemotherapy and radiotherapy only. Hence, we have adopted the protocol using chemotherapy first approach due to logistical reasons. OBJECTIVE: To review the outcome of children diagnosed with high risk medulloblastoma in Hospital Kuala Lumpur. METHODS: Patients diagnosed with high risk medulloblastoma between January 2015 and June 2018 treated using the chemotherapy first approach as per POG9031 protocol were identified. Data was then extracted and analysed. RESULTS: Nine patients were identified, 3 boys and 9 girls. Median age was 9.3 years (range 2.6 – 15.9 years). Median follow up for survivors are 3.6 years. Five patients (55.6%) had macroscopic metastatic disease at diagnosis. All patients had significant residual disease post-op. Only 3 patients are disease free till last follow up, giving a 3 years event free survival of 16%. Of the 6 patients who had relapsed, 4 have died, giving a 3 years overall survival of 46%. Patients with no metastasis at diagnosis (M0) fared better with 3 years event free survival of 38%, but 3 years event free survival for patients with macroscopic metastatic disease (M+) was 0%. CONCLUSION: Outcome of children with high risk medulloblastoma treated with chemotherapy first approach was dismal.
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spelling pubmed-77151032020-12-09 MBCL-50. DISMAL OUTCOME OF HIGH RISK MEDULLOBLASTOMA TREATED WITH CHEMOTHERAPY FIRST APPROACH IN MALAYSIA Quah, Shiao Wei Rahman, E J Abdul Ibrahim, H Mohd Muda, Z Othman, I S Unni, M N Mohamed Gunasagaran, K Ang, M P Goh, C B Teh, K H Neuro Oncol Medulloblastoma (Clinical) INTRODUCTION: Patients with high risk medulloblastoma are treated either with high dose chemotherapy or hyperfractionated radiotherapy. Both approaches are not feasible in resource-limited countries. POG9031 trial has reported favourable outcome for high risk medulloblastoma using standard chemotherapy and radiotherapy only. Hence, we have adopted the protocol using chemotherapy first approach due to logistical reasons. OBJECTIVE: To review the outcome of children diagnosed with high risk medulloblastoma in Hospital Kuala Lumpur. METHODS: Patients diagnosed with high risk medulloblastoma between January 2015 and June 2018 treated using the chemotherapy first approach as per POG9031 protocol were identified. Data was then extracted and analysed. RESULTS: Nine patients were identified, 3 boys and 9 girls. Median age was 9.3 years (range 2.6 – 15.9 years). Median follow up for survivors are 3.6 years. Five patients (55.6%) had macroscopic metastatic disease at diagnosis. All patients had significant residual disease post-op. Only 3 patients are disease free till last follow up, giving a 3 years event free survival of 16%. Of the 6 patients who had relapsed, 4 have died, giving a 3 years overall survival of 46%. Patients with no metastasis at diagnosis (M0) fared better with 3 years event free survival of 38%, but 3 years event free survival for patients with macroscopic metastatic disease (M+) was 0%. CONCLUSION: Outcome of children with high risk medulloblastoma treated with chemotherapy first approach was dismal. Oxford University Press 2020-12-04 /pmc/articles/PMC7715103/ http://dx.doi.org/10.1093/neuonc/noaa222.519 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 Medulloblastoma (Clinical)
Quah, Shiao Wei
Rahman, E J Abdul
Ibrahim, H Mohd
Muda, Z
Othman, I S
Unni, M N Mohamed
Gunasagaran, K
Ang, M P
Goh, C B
Teh, K H
MBCL-50. DISMAL OUTCOME OF HIGH RISK MEDULLOBLASTOMA TREATED WITH CHEMOTHERAPY FIRST APPROACH IN MALAYSIA
title MBCL-50. DISMAL OUTCOME OF HIGH RISK MEDULLOBLASTOMA TREATED WITH CHEMOTHERAPY FIRST APPROACH IN MALAYSIA
title_full MBCL-50. DISMAL OUTCOME OF HIGH RISK MEDULLOBLASTOMA TREATED WITH CHEMOTHERAPY FIRST APPROACH IN MALAYSIA
title_fullStr MBCL-50. DISMAL OUTCOME OF HIGH RISK MEDULLOBLASTOMA TREATED WITH CHEMOTHERAPY FIRST APPROACH IN MALAYSIA
title_full_unstemmed MBCL-50. DISMAL OUTCOME OF HIGH RISK MEDULLOBLASTOMA TREATED WITH CHEMOTHERAPY FIRST APPROACH IN MALAYSIA
title_short MBCL-50. DISMAL OUTCOME OF HIGH RISK MEDULLOBLASTOMA TREATED WITH CHEMOTHERAPY FIRST APPROACH IN MALAYSIA
title_sort mbcl-50. dismal outcome of high risk medulloblastoma treated with chemotherapy first approach in malaysia
topic Medulloblastoma (Clinical)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7715103/
http://dx.doi.org/10.1093/neuonc/noaa222.519
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