Human Neurosciences Department Neurosurgery Division "Sapienza" University, Rome, Italy.
AOU "Policlinico Umberto I", Viale del Policlinico 155, 00161, Rome, Italy.
J Neurooncol. 2020 Jan;146(2):275-284. doi: 10.1007/s11060-019-03364-z. Epub 2019 Dec 30.
In 2019 a group of University of Pennsylvania (Hoffman et al., J Neurooncol 145: 321-328, 2019) aimed to explore the prognostic impact of expression of epidermal growth factor receptor (EGFR), one of the most common genetic alterations in WT-GBM, in young adults with IDH-WT GBM, suggesting an inferior outcomes in young adults (< 45yo) with newly diagnosed, IDH-WT GBM. At the same time, our group were considering the dimension of this subpopulation treated in our centre, and we performed the same analysis, comparing datas with affected elderly adults.
We explore the prognostic impact of EGFR expression status in young adults with IDH-WT GBM, and compare this impact with the affected elderly adults. We therefore analyzed clinical characteristics, tumor genetics, and clinical outcomes in a cohort of adults aged 18-45 years with newly diagnosed WT GBM. We selected a total of 146 patients affected by newly diagnosed IDH-WT GBM who underwent surgery, radiation, and chemotherapy in our Institution in the period ranging between January 2014 and December 2016. We focused primarily on the prognostic impact of EGFR expression.
We confirmed through a Bivariate Analysis that the Age of the Patients, the Volume of the lesions, were statistically strongly associated with the survival parameters; The general OS of the cohort presented a breakthrough point between the patients who were respectively younger and older than 45 years, EGFR mutation was per se not associated to a survival reduction in all the cohort patients. When analyzing exclusively the Survival parameters of the patients whose age was under 40, it was possible to outline a non statistically significant trend towards a lesser OS in younger patients harboring an EGFR expression.
Once again the main difference in terms of OS in GBM is shown in a EOR and in Age. To our knowledge, ours is the second study (Hoffman et al., J Neurooncol 145: 321-328, 2019) to evaluate the prognostic impact of EGFR CN gain specifically in young adults with IDH-WT GBM and in the era of modern radiation and Temozolomide, but is the first one to compares this impact with a population of adults over 45, and correlates this date with clinical onset, dimension and localization of disease between this groups. We suggest other centers to evaluate this important finding with a larger number of patients and we are inclined to accept collaborations to increase the power of this study.
2019 年,宾夕法尼亚大学的一组研究人员(Hoffman 等人,J Neurooncol 145:321-328,2019)旨在探讨表皮生长因子受体(EGFR)表达的预后影响,EGFR 是 WT-GBM 中最常见的遗传改变之一,在 IDH-WT GBM 的年轻患者中,提示年轻患者(<45 岁)的预后较差,这些年轻患者新诊断为 IDH-WT GBM。与此同时,我们的团队正在考虑在我们中心治疗的这个亚群的维度,我们进行了相同的分析,比较了受影响的老年患者的数据。
我们探讨了 EGFR 表达状态在 IDH-WT GBM 的年轻患者中的预后影响,并将其与老年患者的影响进行了比较。因此,我们分析了一组在我们机构新诊断为 WT GBM 的 18-45 岁成年患者的临床特征、肿瘤遗传学和临床结果。我们共选择了 146 名新诊断为 IDH-WT GBM 的患者,这些患者在我们机构接受了手术、放疗和化疗,这些患者的治疗时间在 2014 年 1 月至 2016 年 12 月之间。我们主要关注 EGFR 表达的预后影响。
通过二元分析我们确认了患者的年龄和病变体积与生存参数有统计学上的强相关性;该队列的总 OS 在分别小于和大于 45 岁的患者之间存在突破点,EGFR 突变本身不会导致所有患者的生存时间缩短。当仅分析年龄小于 40 岁的患者的生存参数时,在携带 EGFR 表达的年轻患者中,OS 较短的趋势并不显著。
再次,GBM 中 EOR 和年龄的差异是生存差异的主要原因。据我们所知,我们的研究是第二项(Hoffman 等人,J Neurooncol 145:321-328,2019)专门评估 IDH-WT GBM 中年轻患者 EGFR CN 增益的预后影响,并在现代放疗和替莫唑胺时代进行评估,但这是第一项将这一影响与 45 岁以上成人进行比较的研究,并将这一数据与这两个群体的疾病发病时间、维度和定位相关联。我们建议其他中心用更多的患者来评估这一重要发现,我们倾向于接受合作以增加这项研究的力度。