Mineo Jean-François, Bordron Anne, Baroncini Marc, Maurage Claude-Alain, Ramirez Carole, Siminski Rose-Mary, Berthou Christian, Dam Hieu Phong
Department of Neurosurgery, University Medical Center, Hospital Roger Salengro, 59037 Lille, France.
J Neurooncol. 2007 Dec;85(3):281-7. doi: 10.1007/s11060-007-9424-1. Epub 2007 Jun 15.
Anti-Human Epithelial Receptor Type 2 (HER2) antibodies have the ability to induce in vitro apoptosis of glioblastoma (GBM) cells. This study was designed to evaluate the variability of HER2 expression in GBM and its role as a possible prognosis factor.
Data of 57 patients with GBM and 16 patients with grade III gliomas were retrospectively analyzed. The expression of HER2 was determined by immunohistochemistry and intensity was noted from 0+ to 3+. We compared the HER2 expression in de novo GBM and in GBM resulting from anaplastic transformation of low-grade glioma ("secondary GBM"). Statistical analysis was performed using univariate analysis and the Kaplan-Meier method.
All GBM expressing highly HER2 (2+ and 3+) were de novo GBM. All secondary GBM expressed HER2 with low intensity (0+ and 1+). Survival time was significantly longer when HER2 expression was low (Log Rank test P = 0.04). The patterns of HER2 expression were similar between grade III gliomas and secondary GBM.
To our best knowledge, our study showed for the first time a significant association between HER2 expression and the type of GBM, with subsequent influence on survival rate. GBM with low-HER2 expression are more likely to be secondary GBM, carrying a better prognosis than de novo GBM.
抗人表皮生长因子受体2(HER2)抗体具有在体外诱导胶质母细胞瘤(GBM)细胞凋亡的能力。本研究旨在评估GBM中HER2表达的变异性及其作为可能的预后因素的作用。
回顾性分析57例GBM患者和16例III级神经胶质瘤患者的数据。通过免疫组织化学测定HER2的表达,并记录强度从0 +到3 +。我们比较了原发性GBM和由低级神经胶质瘤间变性转化产生的GBM(“继发性GBM”)中的HER2表达。使用单因素分析和Kaplan-Meier方法进行统计分析。
所有高表达HER2(2 +和3 +)的GBM均为原发性GBM。所有继发性GBM均低强度表达HER2(0 +和1 +)。当HER2表达较低时,生存时间明显更长(对数秩检验P = 0.04)。III级神经胶质瘤和继发性GBM之间HER2表达模式相似。
据我们所知,我们的研究首次表明HER2表达与GBM类型之间存在显著关联,随后对生存率产生影响。低HER2表达的GBM更可能是继发性GBM,其预后比原发性GBM更好。