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酪氨酸激酶抑制剂奥希替尼在EGFR突变型胶质母细胞瘤中的临床活性

Clinical activity of the tyrosine kinase inhibitor osimertinib in -mutant glioblastoma.

作者信息

Makhlin Igor, Salinas Ryan D, Zhang Daniel, Jacob Fadi, Ming Gou-Li, Song Hongjun, Saxena Deeksha, Dorsey Jay F, Nasrallah MacLean P, Morrissette Jennifer Jd, Binder Zev A, O'Rourke Donald M, Desai Arati S, Brem Steven, Bagley Stephen J

机构信息

Division of Hematology & Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

Department of Neurosurgery, University of Pennsylvania, Philadelphia, PA 19104, USA.

出版信息

CNS Oncol. 2019 Nov 1;8(3):CNS43. doi: 10.2217/cns-2019-0014. Epub 2019 Nov 15.

Abstract

Glioblastoma (GBM) is the most common primary malignant brain tumor in adults and carries a dismal prognosis. The gene is among the most commonly deranged genes in GBM and thus an important therapeutic target. We report the case of a young female with heavily pretreated -mutated GBM, for whom we initiated osimertinib, an oral, third-generation tyrosine kinase inhibitor that irreversibly inhibits EGFR and has significant brain penetration. We then review some of the main challenges in targeting EGFR, including lack of central nervous system penetration with most tyrosine kinase inhibitors, molecular heterogeneity of GBM and the need for enhanced specificity for the mutations relevant in GBM.

摘要

胶质母细胞瘤(GBM)是成人中最常见的原发性恶性脑肿瘤,预后不佳。该基因是GBM中最常发生紊乱的基因之一,因此是一个重要的治疗靶点。我们报告了一例年轻女性,患有经过多次治疗的 -突变型GBM,我们为其启动了奥希替尼治疗,奥希替尼是一种口服的第三代酪氨酸激酶抑制剂,可不可逆地抑制表皮生长因子受体(EGFR),且具有显著的脑内渗透性。然后,我们回顾了靶向EGFR的一些主要挑战,包括大多数酪氨酸激酶抑制剂缺乏中枢神经系统渗透性、GBM的分子异质性以及需要增强对GBM相关 突变的特异性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a562/6880297/7555a3de93a3/cns-08-43-g1.jpg

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