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达可替尼:一种用于治疗胶质母细胞瘤的研究性药物。

Dacomitinib: an investigational drug for the treatment of glioblastoma.

机构信息

a Neurooncology Unit , Hospital Universitario 12 de Octubre , Madrid , Spain.

b Neurooncology Unit , Instituto de Salud Carlos III, UFIEC , Madrid , Spain.

出版信息

Expert Opin Investig Drugs. 2018 Oct;27(10):823-829. doi: 10.1080/13543784.2018.1528225. Epub 2018 Oct 5.

Abstract

Standard treatment of newly diagnosed glioblastoma (GB) is surgery with radiotherapy and temozolomide, but tumors will recur with a median overall survival of only 15 months. It seems imperative to explore new possibilities of treatment based on targetable alterations known to be present in GB. Among others, Epidermal Growth Factor Receptor or EGFR (HER1) mutations or amplifications are the most prevalent alterations in GB. In fact, around 40% of GB cases show amplification of EGFR gene, and half of these patients carry the EGFRvIII mutation, a deletion that generates a continuous activation of the tyrosine kinase domain of the receptor. Areas covered: We review the current knowledge about Dacomitinib, an oral, irreversible, second-generation, pan-HER tyrosine kinase inhibitor, in the treatment of glioblastoma. Dacomitinib has noteworthy antiglioma activity in preclinical models and has been tested in one phase II trial in patients with recurrent GB with EGFR amplification. Expert opinion: Despite the poor global results of Dacomitinib in recurrent GB shown in a phase II trial, some patients had a significant benefit. Therefore, it is necessary to improve the knowledge about the mechanisms of failure or resistance to EGFR inhibitors in GB.

摘要

标准治疗新诊断的胶质母细胞瘤(GB)是手术联合放疗和替莫唑胺,但肿瘤会复发,中位总生存期仅为 15 个月。因此,基于已知存在于 GB 中的可靶向改变,探索新的治疗可能性似乎势在必行。在其他改变中,表皮生长因子受体或 EGFR(HER1)突变或扩增是最常见的 GB 改变。事实上,约 40%的 GB 病例显示 EGFR 基因扩增,其中一半患者携带 EGFRvIII 突变,该突变会导致受体酪氨酸激酶结构域的持续激活。涵盖领域:我们回顾了达克替尼的最新知识,达克替尼是一种口服、不可逆、第二代、泛 HER 酪氨酸激酶抑制剂,用于治疗胶质母细胞瘤。达克替尼在临床前模型中具有显著的抗神经胶质瘤活性,并在一项针对 EGFR 扩增的复发性 GB 患者的 II 期试验中进行了测试。专家意见:尽管在 II 期试验中达克替尼在复发性 GB 中的总体结果不佳,但一些患者有显著获益。因此,有必要提高对 GB 中 EGFR 抑制剂失败或耐药机制的认识。

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