Survival after therapy for pediatric ependymoma in a tertiary care center in Saudi Arabia

Author:

Shah Syed Nizam1ORCID,Al-Dandan Sadeq Wasil2,Shuja Muhammad3,Balbaid Ali3,Bashir Mohammad4,Alharbi Musa1

Affiliation:

1. From the Department of Pediatric Hematology and Oncology, King Fahad Medical City, Riyadh, Saudi Arabia

2. From the Department of Pathology and Laboratory Medicine, King Fahad Medical City, Riyadh, Saudi Arabia

3. From the Department of Radiation Oncology, King Fahad Medical City, Riyadh, Saudi Arabia

4. From the Research Center, King Fahad Medical City, Riyadh, Saudi Arabia

Abstract

ABSTRACT 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.

Publisher

King Faisal Specialist Hospital and Research Centre

Subject

General Medicine

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