Massachusetts General Hospital Cancer Center, Boston, MA 02114, USA.
Harvard Medical School, Boston, MA 02115, USA.
Future Oncol. 2020 Mar;16(9):417-425. doi: 10.2217/fon-2019-0647. Epub 2020 Mar 4.
Gene fusions involving , and are oncogenic drivers across a wide variety of cancer types. Inhibitors of the chimeric TRKA/B/C protein kinases encoded by these fusions are now available, including larotrectinib, a potent and highly selective oral drug. Integrated data from three trials demonstrate substantial clinical activity of larotrectinib in patients with many different types of cancers harboring fusions. Larotrectinib has received accelerated approval from both the US FDA and the EMA. Resistance mutations have been observed in the kinase domains of the fusion genes and development of next-generation tropomyosin receptor kinase inhibitors designed to overcome such resistance mutations is being actively pursued in clinical trials and ongoing drug discovery efforts.
涉及 、 和 的基因融合是多种癌症类型的致癌驱动因素。这些融合编码的嵌合 TRKA/B/C 蛋白激酶的抑制剂现在已经可用,包括拉罗替尼,一种强效且高度选择性的口服药物。三项试验的综合数据表明,拉罗替尼在携带 融合的多种不同类型癌症患者中具有显著的临床活性。拉罗替尼已获得美国 FDA 和 EMA 的加速批准。在融合基因的激酶结构域中已经观察到耐药突变,正在临床试验和正在进行的药物发现努力中积极开发设计用于克服这种耐药突变的下一代原肌球蛋白受体激酶抑制剂。