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原肌球蛋白受体激酶抑制剂:2016-2019 年的专利更新回顾。

Tropomyosin receptor kinase inhibitors: an updated patent review for 2016-2019.

机构信息

Department of Oncology, University of Alberta, Cross Cancer Institute, Edmonton, Canada.

Biomedical Chemistry, Department of Clinical Radiology and Nuclear Medicine, Medical Faculty Mannheim of Heidelberg University, Mannheim, Germany.

出版信息

Expert Opin Ther Pat. 2020 May;30(5):325-339. doi: 10.1080/13543776.2020.1737011. Epub 2020 Mar 10.

Abstract

: Tropomyosin receptor kinases (Trks) control processes in the fields of growth, survival, and differentiation of neuronal processes. They also play a crucial role in neurodegenerative diseases as well as different types of cancer. Interest in developing Trk inhibitors to target fusion-driven cancers has escalated in the last decade, leading to the FDA approval of the pan-Trk inhibitors entrectinib and larotrectinib. The development of next-generation inhibitors that overcome resistance mutations arising from treatment with these first generation inhibitors has been the focus in recent years.: In this updated patent review for 2016-2019, patents covering inhibitors targeting the Trk family are discussed as a continuation of the previous reviews, . The status of Trk inhibitors in clinical trials is also evaluated. For the identification of relevant patents and clinical trials, Web of Science, Google, Google Patents, and patent referencing were used.: The FDA approval of larotrectinib and entrectinib is a prime example of how basket clinical trial design targeting oncogenic drivers, regardless of tumor histology, is a viable approach to drug discovery and embodies the shift toward personalized medicine.

摘要

: 原肌球蛋白受体激酶(Trks)控制着神经元过程生长、存活和分化等过程。它们在神经退行性疾病和不同类型的癌症中也起着至关重要的作用。在过去十年中,人们对开发针对融合驱动癌症的 Trk 抑制剂的兴趣日益浓厚,这导致了泛 Trk 抑制剂恩曲替尼和拉罗替尼获得 FDA 批准。近年来的重点是开发克服这些第一代抑制剂治疗产生的耐药性突变的下一代抑制剂。

: 在本更新的 2016-2019 年专利综述中,作为前几次综述的延续,讨论了针对 Trk 家族的抑制剂专利。还评估了 Trk 抑制剂在临床试验中的状况。为了确定相关专利和临床试验,使用了 Web of Science、Google、Google Patents 和专利参考文献。

: FDA 批准拉罗替尼和恩曲替尼是一个很好的例子,说明针对致癌驱动因素的篮子临床试验设计,无论肿瘤组织学如何,都是一种可行的药物发现方法,体现了向个性化医疗的转变。

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