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

被引:24
作者
Bailey, Justin J. [1 ]
Jaworski, Carolin [1 ]
Tung, Donovan [1 ]
Waengler, Carmen [2 ]
Waengler, Bjoern [3 ]
Schirrmacher, Ralf [1 ]
机构
[1] Univ Alberta, Cross Canc Inst, Dept Oncol, 11560 Univ Ave, Edmonton, AB T6G 1Z2, Canada
[2] Heidelberg Univ, Biomed Chem, Dept Clin Radiol & Nucl Med, Med Fac Mannheim, Mannheim, Germany
[3] Heidelberg Univ, Mol Imaging & Radiochem, Dept Clin Radiol & Nucl Med, Med Fac Mannheim, Mannheim, Germany
关键词
Tropomyosin receptor kinase; TrkA; TrkB; TrkC; NTRK; Trk inhibitor; cancer treatment; chronic pain; entrectinib; larotrectinib; targeted therapy; selitrectinib; resistance mutations; allosteric inhibitors; ACQUIRED-RESISTANCE; FUSION; CRIZOTINIB; NEUROTROPHINS; LAROTRECTINIB; ONCOGENE; BLOCKING; EFFICACY; MUTATION; POTENT;
D O I
10.1080/13543776.2020.1737011
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Introduction: 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 NTRK 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. Area covered: In this updated patent review for 2016-2019, patents covering inhibitors targeting the Trk family are discussed as a continuation of the previous reviews, Tropomyosin receptor kinase inhibitors: an updated patent review for 2010-2016 - Parts 1 & 2. 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. Expert opinion: 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.
引用
收藏
页码:325 / 339
页数:15
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