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阿伐替尼用于治疗转移性或不可切除的胃肠道间质瘤。

Avapritinib for metastatic or unresectable gastrointestinal stromal tumors.

作者信息

Alzofon N, Jimeno A

机构信息

Division of Medical Oncology, Department of Medicine, University of Colorado School of Medicine, Aurora, Colorado, USA.

Division of Medical Oncology, Department of Medicine and Charles C. Gates Center for Regenerative Medicine and Stem Cell Biology, University of Colorado School of Medicine, Aurora, Colorado, USA.

出版信息

Drugs Today (Barc). 2020 Sep;56(9):561-571. doi: 10.1358/dot.2020.56.9.3170808.

Abstract

Avapritinib is a tyrosine kinase inhibitor (TKI) that has recently received Food and Drug Administration (FDA) approval for the treatment of metastatic or unresectable gastrointestinal stromal tumors harboring a platelet-derived growth factor receptor alpha (PDGFRA) exon 18 mutation. Mutations in the activation loop of PDGFRA or KIT confer resistance to conventional TKIs due to structural changes in the receptor. Avapritinib was developed to selectively target these mutations, thereby offering a new treatment option for patients in whom imatinib, sunitinib, and regorafenib have failed. This review covers the basic science and preclinical studies that guided avapritinib's development, in addition to the data currently available from early clinical studies as well as those later-stage trials that led to its approval.

摘要

阿伐普替尼是一种酪氨酸激酶抑制剂(TKI),最近已获得美国食品药品监督管理局(FDA)批准,用于治疗携带血小板衍生生长因子受体α(PDGFRA)外显子18突变的转移性或不可切除的胃肠道间质瘤。由于受体结构变化,PDGFRA或KIT激活环中的突变会导致对传统TKI产生耐药性。开发阿伐普替尼是为了选择性地靶向这些突变,从而为伊马替尼、舒尼替尼和瑞戈非尼治疗失败的患者提供一种新的治疗选择。本综述涵盖了指导阿伐普替尼研发的基础科学和临床前研究,以及目前早期临床研究和导致其获批的后期试验中可获得的数据。

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