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Annals of Saudi medicine. 2020 Nov-Dec;40(6):482-490. doi: 10.5144/0256-4947.2020.482

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

沙特阿拉伯一家三级医疗中心儿科室管细胞瘤治疗后的生存率 翻译改进

Syed Nizam Shah  1, Sadeq Wasil Al-Dandan  2, Muhammad Shuja  3, Ali Balbaid  3, Mohammad Bashir  4, Musa Alharbi  1

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作者单位

  • 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.
  • DOI: 10.5144/0256-4947.2020.482 PMID: 33307736

    摘要 Ai翻译

    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.

    Keywords:pediatric ependymoma; survival

    Copyright © Annals of Saudi medicine. 中文内容为AI机器翻译,仅供参考!

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