Johnson Derek R, Wefel Jeffrey S
Department of Neurology, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.
CNS Oncol. 2013 Mar;2(2):195-201. doi: 10.2217/cns.13.5.
The association between increased signs and symptoms and poorer survival in glioblastoma is well recognized and confirmed in virtually every clinical trial and patient series. Measurement and consideration of performance status is, therefore, vital when counseling patients regarding their expected survival or evaluating the results of clinical trials. Unfortunately, measures of patient function in clinical trials have remained quite crude, in stark contrast to the rapid advances seen in the pathological characterization of brain tumors. Recently, clinical investigators have begun to examine the subcomponents of performance status in more detail, revealing that objective measures of cognition are significantly associated with patient survival in both newly diagnosed and recurrent glioblastoma. Furthermore, cognitive function does not appear to be a simple proxy for performance status but rather an independent predictor of survival, even within patient groups defined by currently available clinical prognostic systems. Therefore, objective measures of cognition must be evaluated for inclusion in future prognostic models and the simple addition of new tumor biomarkers to the current clinical prognostic models will likely prove insufficient. In order for the field of neuro-oncology to move forward in this regard, evaluation of cognition must become a routine part of future clinical trials, and the data must be recorded and analyzed with the same diligence as other trial end points.
胶质母细胞瘤中体征和症状增加与较差生存率之间的关联在几乎每一项临床试验和患者系列研究中都得到了充分认识和证实。因此,在向患者咨询其预期生存期或评估临床试验结果时,对其功能状态进行测量和考量至关重要。不幸的是,与脑肿瘤病理特征方面取得的快速进展形成鲜明对比的是,临床试验中对患者功能的测量仍相当粗略。最近,临床研究人员已开始更详细地研究功能状态的子成分,结果显示,无论是新诊断还是复发的胶质母细胞瘤,认知的客观测量指标都与患者生存率显著相关。此外,认知功能似乎并非功能状态的简单替代指标,而是生存率的独立预测因素,即使在由当前可用临床预后系统定义的患者群体中也是如此。因此,必须评估认知的客观测量指标,以便纳入未来的预后模型,而且仅在当前临床预后模型中简单添加新的肿瘤生物标志物可能证明是不够的。为了神经肿瘤学领域在这方面取得进展,认知评估必须成为未来临床试验的常规组成部分,并且必须像对待其他试验终点一样认真记录和分析相关数据。
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