Mazaris Paul, Hong Xin, Altshuler David, Schultz Lonni, Poisson Laila M, Jain Rajan, Mikkelsen Tom, Rosenblum Mark, Kalkanis Steven
Departments of Neurosurgery, Hermelin Brain Tumor Center, Henry Ford Health System, 2799 West Grand Boulevard, Detroit 48202, USA.
Wayne State University School of Medicine, 1313 Scott Hall, Detroit 48201, USA.
Clin Neurol Neurosurg. 2014 May;120:103-12. doi: 10.1016/j.clineuro.2014.03.001. Epub 2014 Mar 12.
Glioblastoma (GBM) is a heterogeneous neoplasm with a small percentage of long-term survivors. Despite aggressive surgical resection and advances in radiotherapy and chemotherapy, the median survival for patients with GBM is 12-14 months. Factors associated with a favorable prognosis include young age, high performance status, gross resection >98%, non-eloquent tumor location and O6-methylguanine methyltransferase (MGMT) promoter methylation. We retrospectively analyzed the relationship of clinical, epidemiologic, genetic and molecular characteristics with survival in patients with GBM.
This retrospective analysis of overall survival looked at the outcomes of 480 patients diagnosed with GBM over 14 years at a single institution. Multivariate analysis was performed examining multiple patient characteristics.
Median survival time improved from 11.8 months in patients diagnosed from 1995 to 1999 to 15.9 months in those diagnosed from 2005 to 2008. Factors associated with survivor groups were age, KPS, tumor resection, treatment received and early progression. 18 cancer-related genes were upregulated in short-term survivors and five genes were downregulated in short-term survivors.
Epidemiologic, clinical, and molecular characteristics all contribute to GBM prognosis. Identifying factors associated with survival is important for treatment strategies as well as research for novel therapeutics and technologies. This study demonstrated improved survival for patients over time as well as significant differences among survivor groups.
胶质母细胞瘤(GBM)是一种异质性肿瘤,长期存活者比例较低。尽管进行了积极的手术切除以及放疗和化疗取得了进展,但GBM患者的中位生存期为12 - 14个月。与良好预后相关的因素包括年轻、高功能状态、大体切除率>98%、肿瘤位于非功能区以及O6 - 甲基鸟嘌呤甲基转移酶(MGMT)启动子甲基化。我们回顾性分析了GBM患者的临床、流行病学、遗传和分子特征与生存的关系。
这项对总生存期的回顾性分析考察了在单一机构14年间诊断为GBM的480例患者的结局。进行多变量分析以检验多个患者特征。
中位生存时间从1995年至1999年诊断的患者的11.8个月提高到2005年至2008年诊断的患者的15.9个月。与生存组相关的因素是年龄、KPS、肿瘤切除、接受治疗情况和早期进展。18个癌症相关基因在短期存活者中上调,5个基因在短期存活者中下调。
流行病学、临床和分子特征均对GBM预后有影响。确定与生存相关的因素对于治疗策略以及新型治疗方法和技术的研究都很重要。本研究表明患者的生存期随时间有所改善,且生存组之间存在显著差异。