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Adult Spinal Ependymomas: An Epidemiologic Study.
Syed I Khalid1, Owoicho Adogwa1, Ryan Kelly2
1Department of Neurosurgery, Rush University Medical Center, Chicago, Illinois.
World Neurosurgery
|December 12, 2017
Summary
Spinal ependymomas in adults are rare. High-grade tumors, older age, and radiation therapy are linked to worse survival, while gross total resection improves outcomes.
Area of Science:
- Neuro-oncology
- Epidemiology
- Cancer Survival Analysis
Background:
- Spinal ependymomas are rare central nervous system tumors in adults, comprising 3-6% of cases.
- Their rarity and poor prognosis necessitate population-based studies to identify survival factors and improve patient outcomes.
Purpose of the Study:
- To investigate epidemiological factors and survival risk associated with adult spinal ependymomas.
- To identify predictors of improved or decreased survival in this patient population.
Main Methods:
- Retrospective analysis of histologically confirmed spinal ependymomas in adults (≥18 years) using the Surveillance, Epidemiology, and End Results (SEER) database.
- Kaplan-Meier survival curves and multivariate regression analysis were employed to assess survival predictors.
Main Results:
- Five-year overall survival was 93.3%.
- Factors associated with decreased survival include older age at diagnosis, high tumor grade (grade IV), and use of radiation therapy.
- Gross total resection was associated with improved overall survival.
Conclusions:
- High-grade spinal ependymomas carry a significantly worse prognosis compared to lower-grade tumors.
- Early diagnosis and surgical resection are linked to better survival outcomes.
- The role of radiation therapy in spinal ependymoma treatment remains unclear.
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