Prognostic significance of CT contrast enhancement within histological subgroups of intracranial glioma

被引:35
作者
Lote, K [1 ]
Egeland, T
Hager, B
Skullerud, K
Hirschberg, H
机构
[1] Norwegian Radium Hosp, Dept Oncol, N-0310 Oslo, Norway
[2] Norwegian Radium Hosp, Dept Radiol, N-0310 Oslo, Norway
[3] Univ Oslo, Natl Hosp, Dept Pathol, Oslo, Norway
[4] Univ Oslo, Natl Hosp, Dept Neurosurg, Oslo, Norway
[5] Univ Oslo, Natl Hosp, Ctr Epidemiol & Hosp Stat, Oslo, Norway
关键词
contrast enhancement; prognostic factor; specificity; glioma;
D O I
10.1023/A:1006106708606
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We report the prognostic significance of tumor CT contrast enhancement within histological subgroups in 831 consecutive adult glioma patients of high-grade (n = 516) and low-grade (n = 315) histology. In the present report, a negative prognostic factor is associated with shortened survival. Methods: Survival analysis including Kaplan-Meier plots, log-rank tests, Cox analysis, and Aalen's linear model as implemented in SPSS and S-PLUS. Results: Sensitivity and specificity of contrast enhancement as a test for high-grade glioma was 0.87 and 0.79, respectively. Enhancement was a strong negative prognostic factor comparable to high-grade histology in the total patient population. Enhancement was also a negative prognostic factor within the subgroups adult high-grade (Grade 3-4), anaplastic (Grade 3), and low-grade (Grade 1-2) gliomas (p < 0.001). The prognostic implications of initial enhancement declined in high-grade patients surviving beyond 36 months. Tumor contrast enhancement or calcifications (in parentheses) were present in 96% (3.6%) of glioblastomas, in 87% (7.4%) of high-grade gliomas, in 56.5% of anaplastic gliomas, and in 21% (16.2%) of low-grade gliomas. Calcification was a positive prognostic factor within the high-grade group of patients (p < 0.0001). Conclusion: Enhancement was a major prognostic factor comparable to high-grade: histology in this glioma patient population. Enhancement was a negative prognostic factor within each of the adult subgroups high-grade, anaplastic (grade 3), and low-grade gliomas. Enhancement was strongly associated with but not pathognomonic for high-grade histology.
引用
收藏
页码:161 / 170
页数:10
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