Berghoff Anna S, Preusser Matthias
Institute of Neurology, Department of Medicine I, Medical University of Vienna, and Comprehensive Cancer Center Vienna - CNS Tumors Unit, Vienna, Austria.
Clin Neuropathol. 2012 Nov-Dec;31(6):405-8. doi: 10.5414/np300576.
In 2005, a seminal paper showed that glioblastoma patients aged 18 to 70, whose tumors have a methylated MGMT promoter have a better prognosis than patients with tumors carrying an unmethylated MGMT promoter. As a consequence of this and several confirmatory studies, routine MGMT testing in the clinical setting was promoted. However, only few centers have indeed implemented routine clinical MGMT testing, mostly due the lack of clear clinical consequence and because of considerable technical issues with the testing itself. Recently published results of trials on elderly patients with malignant gliomas have revived the call for routine MGMT testing for clinical decision making. These studies strongly support that MGMT status is a predictive factor for response to temozolomide treatment in elderly patients with malignant astrocytic gliomas and its use for therapy decisions could improve patient management, avoid treatment toxicities and save costs. However, although a number of different protocols for MGMT testing from routinely collected and formalin-fixed and paraffin-embedded tissue have been suggested, there is still no commonly accepted test method with sufficient analytical performance. Protocols established in high-throughput specialized academic or commercial laboratories may not be easily transferable to less specialized laboratories. Thus, before MGMT testing can be used and recommended for clinical decision making, an adequate test method with confirmed high repeatability and reproducibility needs to be identified. To this end, specifically designed investigations including stringently controlled interlaboratory ring trials are needed. Such studies need to take into account the considerable variation in pre-analytical tissue handling (e.g., tissue fixation conditions) between laboratories.
2005年,一篇具有开创性的论文表明,年龄在18至70岁之间的胶质母细胞瘤患者,其肿瘤的MGMT启动子发生甲基化,其预后要优于MGMT启动子未甲基化的肿瘤患者。基于这一研究及多项验证性研究的结果,临床环境中常规的MGMT检测得到了推广。然而,实际上只有少数中心实施了常规的临床MGMT检测,主要原因是缺乏明确的临床意义,以及检测本身存在诸多技术问题。最近发表的老年恶性胶质瘤患者试验结果再次呼吁进行常规MGMT检测以用于临床决策。这些研究有力地支持了MGMT状态是老年恶性星形细胞瘤患者对替莫唑胺治疗反应的预测因素,将其用于治疗决策可改善患者管理、避免治疗毒性并节省成本。然而,尽管已经提出了许多从常规收集的、福尔马林固定石蜡包埋组织中进行MGMT检测的不同方案,但仍然没有一种具有足够分析性能且被普遍接受的检测方法。在高通量专业学术或商业实验室建立的方案可能不容易转移到不太专业的实验室。因此,在MGMT检测能够用于并被推荐用于临床决策之前,需要确定一种具有高重复性和再现性的合适检测方法。为此,需要进行专门设计的调查,包括严格控制的实验室间环形试验。此类研究需要考虑到不同实验室之间在分析前组织处理(如组织固定条件)方面的巨大差异。