Li Gordon, Mitra Siddhartha, Wong Albert J
Department of Neurosurgery, Stanford University School of Medicine, 300 Pasteur Drive, Edwards Building Room 213, Stanford, CA 94305, USA.
Neurosurg Clin N Am. 2010 Jan;21(1):87-93. doi: 10.1016/j.nec.2009.08.004.
Epidermal growth factor variant III (EGFRvIII) is the most common alteration of the epidermal growth factor (EGF) receptor found in human tumors. It is commonly expressed in glioblastoma multiforme (GBM), where it was initially identified. This constitutively active mutant receptor leads to unregulated growth, survival, invasion, and angiogenesis in cells that express it. EGFRvIII results from an in-frame deletion of exons 2 to 7 resulting in the fusion of exon 1 to exon 8 of the EGF receptor gene creating a novel glycine at the junction in the extracellular amino terminal domain. The juxtaposition of ordinarily distant amino acids in combination with the glycine that forms at the junction leads to a novel tumor-specific epitope that would make an ideal tumor-specific target. A peptide derived from the EGFRvIII junction can be used as a vaccine to prevent or induce the regression of tumors. This peptide vaccine has now proceeded to phase 1 and 2 clinical trials where it has been highly successful and is now undergoing investigation in a larger human clinical trial for patients who have newly diagnosed GBM. In this article, the authors discuss the preclinical data that led to the human trials and the exciting preliminary data from the clinical trials.
表皮生长因子变异体III(EGFRvIII)是在人类肿瘤中发现的表皮生长因子(EGF)受体最常见的变异形式。它最初是在多形性胶质母细胞瘤(GBM)中被鉴定出来的,在该肿瘤中普遍表达。这种组成型激活的突变受体导致表达它的细胞中生长、存活、侵袭和血管生成不受调控。EGFRvIII是由外显子2至7的框内缺失导致的,从而使表皮生长因子受体基因的外显子1与外显子8融合,在细胞外氨基末端结构域的连接处产生一个新的甘氨酸。通常相距较远的氨基酸并列,再加上连接处形成的甘氨酸,导致形成一个新的肿瘤特异性表位,这将成为一个理想的肿瘤特异性靶点。源自EGFRvIII连接处的一种肽可作为疫苗用于预防肿瘤或诱导肿瘤消退。这种肽疫苗现已进入1期和2期临床试验,在这些试验中取得了巨大成功,目前正在针对新诊断的GBM患者进行更大规模的人体临床试验研究。在本文中,作者讨论了促成人体试验的临床前数据以及来自临床试验的令人振奋的初步数据。