Kwatra Madan M
Duke University Medical Center, Durham, P.O. Box 3094, NC 27710, United States.
Curr Cancer Drug Targets. 2017;17(3):290-296. doi: 10.2174/1568009616666161227091522.
Glioblastoma (GBM) is a deadly brain cancer, and all attempts to control it have failed so far. However, the future looks bright, as we now know the molecular landscape of GBM through the work of The Cancer Genome Atlas (TCGA) program. GBMs exhibit significant inter- and intratumoral heterogeneity, and to control this type of tumor, a personalized approach is required. One target, whose gene is amplified and mutated in a large number of GBMs, is the epidermal growth factor receptor (EGFR). But all attempts to target it have been unsuccessful. We attribute the reason for this failure to the molecular heterogeneity of EGFR in GBM, as well as to the poor brain penetration of previously tested EGFR-Tyrosine Kinase Inhibitors (EGFR-TKIs). In this review, we discuss the molecular heterogeneity of EGFR and provide rational preclinical and clinical guidelines for testing AZD9291, a third generation, irreversible EGFR-TKI with both a high affinity for EGFRvIII and excellent brain penetration.
胶质母细胞瘤(GBM)是一种致命的脑癌,迄今为止,所有控制它的尝试均告失败。然而,未来前景光明,因为通过癌症基因组图谱(TCGA)项目的工作,我们现在已经了解了GBM的分子格局。GBM表现出显著的肿瘤间和肿瘤内异质性,为了控制这类肿瘤,需要采用个性化方法。在大量GBM中,其基因发生扩增和突变的一个靶点是表皮生长因子受体(EGFR)。但所有针对它的尝试均未成功。我们将这种失败的原因归因于GBM中EGFR的分子异质性,以及先前测试的EGFR酪氨酸激酶抑制剂(EGFR-TKIs)较差的脑渗透性。在本综述中,我们讨论了EGFR的分子异质性,并为测试AZD9291提供合理的临床前和临床指南,AZD9291是第三代不可逆EGFR-TKI,对EGFRvIII具有高亲和力且脑渗透性良好。