Pretreatment factors predict overall survival for patients with low-grade glioma: A recursive partitioning analysis

被引:144
作者
Bauman, G
Lote, K
Larson, D
Stalpers, L
Leighton, C
Fisher, B
Wara, W
MacDonald, D
Stitt, L
Cairncross, JG
机构
[1] London Reg Canc Ctr, Dept Radiat Oncol, London, ON N6A 4L6, Canada
[2] Univ Western Ontario, Dept Oncol, London, ON, Canada
[3] Univ Western Ontario, Dept Epidemiol & Biostat, London, ON, Canada
[4] Univ Western Ontario, Dept Clin Neurol Sci, London, ON, Canada
[5] Univ Calif San Francisco, Dept Radiat Oncol, San Francisco, CA USA
[6] Amsterdam Med Ctr, Dept Radiat Oncol, Amsterdam, Netherlands
[7] Norwegian Radium Hosp, Dept Oncol, Oslo, Norway
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 1999年 / 45卷 / 04期
关键词
low-grade glioma; astrocytoma; oligodendroglioma; mixed oligoastrocytoma; prognostic factors; radiotherapy; outcome;
D O I
10.1016/S0360-3016(99)00284-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Three databases were pooled and analyzed to determine which groupings of prognostic factors best predicted overall survival for patients with low-grade gliomas treated with surgery and immediate or delayed radiotherapy. Methods and Materials: Databases of patients with low-grade gliomas compiled at the London Regional Cancer Centre (LRCC), the Norwegian Radium Hospital (NRH), and the University of California, San Francisco (UCSF) were merged. Inclusion criteria for the pooled analysis included: age greater than or equal to 18 years and histologically confirmed low-grade (World Health Organization Grade II) supratentorial fibrillary astrocytoma, oligodendroglioma or mixed oligoastrocytoma. Factors analyzed for prognostic significance included: age at diagnosis, gender, seizures at presentation, presence of enhancement on computed tomography (CT) or magnetic resonance imaging (MRI), Karnofsky Performance Status (KPS) at diagnosis, histology, extent of surgical resection, timing of radiotherapy, and treating institution. Univariate and multivariate analysis of overall survival for these factors was performed. Recursive partitioning was performed to generate prognostic groups using these factors. Results: From the combined databases, 401 patients were eligible for analysis. Median survival for the entire group,vas 95 months/7.9 years. On univariate analysis age 18-40, presence of seizures at presentation, KPS greater than or equal to 70, treating institution, and absence of contrast enhancement were associated with improved overall survival. On multivariate analysis, these factors remained independent predictors of improved overall survival. Recursive partitioning analysis yielded four prognostic groups with statistically different median survivals (MS): Group I (n = 41: KPS < 70, age > 40) MS 12 months; Group II (n = 34: KPS greater than or equal to 70, age > 40, enhancement present) MS 46 months; Group III (n = 138: KPS < 70, age 18-40 or KPS greater than or equal to 70 age > 40, no enhancement) MS 87 months; Group IV (n = 188: KPS greater than or equal to 70, age 18-40) MS 128 months. Conclusion: Clusters of pretreatment prognostic factors described subgroups of low-grade glioma patients with divergent overall survivals. Consideration of these prognostic subgroups may be important when considering timing of interventions for these patients and in the stratification of patients for clinical trials. (C) 1999 Elsevier Science Inc.
引用
收藏
页码:923 / 929
页数:7
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