A retrospective analysis of 52 cases of spinal cord glioma managed with radiation therapy

被引:46
作者
Rodrigues, GB [1 ]
Waldron, JN [1 ]
Wong, CS [1 ]
Laperriere, NJ [1 ]
机构
[1] Univ Toronto Hlth Network, Princess Margaret Hosp, Ontario Canc Inst, Dept Radiat Oncol, Toronto, ON M5G 2M9, Canada
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2000年 / 48卷 / 03期
关键词
spinal cord; glioma; radiation therapy;
D O I
10.1016/S0360-3016(00)00690-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To describe the outcome of primary spinal cord glioma treated with radiation therapy after surgery and to identify variables predictive of outcome. Methods and Materials: A chart review of 52 patients with a diagnosis of spinal cord non-ependymoma glioma at the Princess Margaret Hospital was conducted. Thirty-two patients (62%) were male and 20 (38%) were female. Median age was 32 years (2-76 years). Median follow-up was 3.7 years (2 months to 27 years). Initial surgical management consisted of biopsy alone in 27 (52%) cases, subtotal resection in 20 (38%) cases, and gross total resection in 5 (10%) cases. All patients received postoperative radiation therapy; median total dose was 50 Gy, given in 25 daily fractions (20-60 Gy). Actuarial survival rates were calculated and the influence of patient-, tumor-, and treatment-related variables on outcome was determined. Results: Five-year overall, cause-specific, and progression-free survivals were 54%, 62%, and 58%, respectively. Ten-year survivals were 45%, 50%, and 43%, respectively. A total of 29 (56%) patients died during the period of review. For 23 (79%) of these patients, death was cancer specific. Progression of tumor was documented in 28 of 52 (54%) patients. The following factors predicted for improved outcome on univariate analysis: age < 18 years, low-grade histology, and length of symptoms prior to diagnosis > 6 months. Conclusion: The outcome of patients in this series is consistent with that of other similar published reports. Specific recommendations are made for the management of this tumor. (C) 2000 Elsevier Science Inc.
引用
收藏
页码:837 / 842
页数:6
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