Survival after therapy for pediatric ependymoma in a tertiary care center in Saudi Arabia
BACKGROUND: There is limited data from Saudi Arabia on the demographic characteristics, outcomes and effectiveness of different treatment modalities in children with intracranial ependymoma. OBJECTIVE: Study the characteristics of pediatric ependymoma and outcomes of treatment modalities in Saudi Ar...
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King Faisal Specialist Hospital and Research Centre
2020-12-01
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doaj-0f5eab3aaec34e7f801ace2bf86d64832020-12-18T13:32:45ZengKing Faisal Specialist Hospital and Research CentreAnnals of Saudi Medicine0256-49470975-44662020-12-0140648249010.5144/0256-4947.2020.4820256-4947.2020.482Survival after therapy for pediatric ependymoma in a tertiary care center in Saudi ArabiaSyed Nizam Shah0Sadeq Wasil Al-Dandan1Muhammad Shuja2Ali Balbaid3Mohammad Bashir4Musa Alharbi5From the Department of Pediatric Hematology and Oncology, King Fahad Medical City, Riyadh, Saudi ArabiaFrom the Department of Pathology and Laboratory Medicine, King Fahad Medical City, Riyadh, Saudi ArabiaFrom the Department of Radiation Oncology, King Fahad Medical City, Riyadh, Saudi ArabiaFrom the Department of Radiation Oncology, King Fahad Medical City, Riyadh, Saudi ArabiaFrom the Research Center, King Fahad Medical City, Riyadh, Saudi ArabiaFrom the Department of Pediatric Hematology and Oncology, King Fahad Medical City, Riyadh, Saudi ArabiaBACKGROUND: There is limited data from Saudi Arabia on the demographic characteristics, outcomes and effectiveness of different treatment modalities in children with intracranial ependymoma. OBJECTIVE: Study the characteristics of pediatric ependymoma and outcomes of treatment modalities in Saudi Arabia. DESIGN: Retrospective. SETTING: Tertiary care center. PATIENTS AND METHODS: Children with intracranial ependymoma who were younger than 14 years of age and treated between 2006 and 2015 were included in the study. Patients with prior radiation, chemo-therapy, or surgical resection at other centers were excluded. MAIN OUTCOME MEASURES: Kaplan-Meier survival curves were used to estimate the event-free (EFS) and overall survival (OS) rates of the patients. SAMPLE SIZE: 22. RESULTS: Of the 22 children, 4 (18.2%) were less than three years old. All intracranial ependymomas had upfront surgical resection of the primary tumor. Gross total resection was achievable in 9 (42.9%) cases and subtotal resection in another 9 (42.9%). Near-total resection was done in 3 (14.3%) cases. Median time from surgery to start of radiotherapy was 62 days. RT was given to 17 (77.3%) patients. Both mean and median RT dose was 55.8 Gy. Only 5 (22.7%) of the children received chemotherapy. The median duration of follow-up was 5.38 years and the median time for EFS was 2.27 years. The cumulative OS rate of the study was 44.5%. The cumulative EFS survival rate of the study was 18.6%. Among demographic, pathological, radiological features, none had a statistically significant effect on the survival. CONCLUSIONS: The outcomes are comparable to those reported by international investigators for similar populations. Further improvements can be achieved by avoiding delays in radiation therapy and adding molecular staging. LIMITATIONS: The limited number of cases, retrospective nature, lack of molecular biology and size of the tumors. CONFLICT OF INTEREST: None.https://www.annsaudimed.net/doi/full/10.5144/0256-4947.2020.482 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Syed Nizam Shah Sadeq Wasil Al-Dandan Muhammad Shuja Ali Balbaid Mohammad Bashir Musa Alharbi |
spellingShingle |
Syed Nizam Shah Sadeq Wasil Al-Dandan Muhammad Shuja Ali Balbaid Mohammad Bashir Musa Alharbi Survival after therapy for pediatric ependymoma in a tertiary care center in Saudi Arabia Annals of Saudi Medicine |
author_facet |
Syed Nizam Shah Sadeq Wasil Al-Dandan Muhammad Shuja Ali Balbaid Mohammad Bashir Musa Alharbi |
author_sort |
Syed Nizam Shah |
title |
Survival after therapy for pediatric ependymoma in a tertiary care center in Saudi Arabia |
title_short |
Survival after therapy for pediatric ependymoma in a tertiary care center in Saudi Arabia |
title_full |
Survival after therapy for pediatric ependymoma in a tertiary care center in Saudi Arabia |
title_fullStr |
Survival after therapy for pediatric ependymoma in a tertiary care center in Saudi Arabia |
title_full_unstemmed |
Survival after therapy for pediatric ependymoma in a tertiary care center in Saudi Arabia |
title_sort |
survival after therapy for pediatric ependymoma in a tertiary care center in saudi arabia |
publisher |
King Faisal Specialist Hospital and Research Centre |
series |
Annals of Saudi Medicine |
issn |
0256-4947 0975-4466 |
publishDate |
2020-12-01 |
description |
BACKGROUND: There is limited data from Saudi Arabia on the demographic characteristics, outcomes and effectiveness of different treatment modalities in children with intracranial ependymoma. OBJECTIVE: Study the characteristics of pediatric ependymoma and outcomes of treatment modalities in Saudi Arabia. DESIGN: Retrospective. SETTING: Tertiary care center. PATIENTS AND METHODS: Children with intracranial ependymoma who were younger than 14 years of age and treated between 2006 and 2015 were included in the study. Patients with prior radiation, chemo-therapy, or surgical resection at other centers were excluded. MAIN OUTCOME MEASURES: Kaplan-Meier survival curves were used to estimate the event-free (EFS) and overall survival (OS) rates of the patients. SAMPLE SIZE: 22. RESULTS: Of the 22 children, 4 (18.2%) were less than three years old. All intracranial ependymomas had upfront surgical resection of the primary tumor. Gross total resection was achievable in 9 (42.9%) cases and subtotal resection in another 9 (42.9%). Near-total resection was done in 3 (14.3%) cases. Median time from surgery to start of radiotherapy was 62 days. RT was given to 17 (77.3%) patients. Both mean and median RT dose was 55.8 Gy. Only 5 (22.7%) of the children received chemotherapy. The median duration of follow-up was 5.38 years and the median time for EFS was 2.27 years. The cumulative OS rate of the study was 44.5%. The cumulative EFS survival rate of the study was 18.6%. Among demographic, pathological, radiological features, none had a statistically significant effect on the survival. CONCLUSIONS: The outcomes are comparable to those reported by international investigators for similar populations. Further improvements can be achieved by avoiding delays in radiation therapy and adding molecular staging. LIMITATIONS: The limited number of cases, retrospective nature, lack of molecular biology and size of the tumors. CONFLICT OF INTEREST: None. |
url |
https://www.annsaudimed.net/doi/full/10.5144/0256-4947.2020.482 |
work_keys_str_mv |
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