临床开发多靶点酪氨酸激酶抑制剂:重点是XL-184 (cabozantinib)。

IF 1.8 4区 医学 Q2 Medicine
D W Bowles, E R Kessler, A Jimeno
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引用次数: 33

摘要

XL-184 (cabozantinib)是一种新型的小分子多靶点酪氨酸激酶抑制剂,对肝细胞生长因子受体(酪氨酸-蛋白激酶Met)、血管内皮生长因子受体2 (VEGFR-2)和原癌基因酪氨酸-蛋白激酶受体Ret具有特殊的活性。有充分的证据表明Met、VEGFR-2和Ret信号传导在几种肿瘤类型中。临床前数据表明,XL-184在上皮和间充质来源的肿瘤中都有活性。I期和II期临床研究支持显著的抗肿瘤活性,特别是在甲状腺髓样癌和骨转移癌中。本综述将评估XL-184的临床前药理学、药代动力学、药物相互作用和I - III期临床活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multi-targeted tyrosine kinase inhibitors in clinical development: focus on XL-184 (cabozantinib).

XL-184 (cabozantinib) is a novel, small-molecule, multitargeted receptor tyrosine kinase inhibitor with particular activity against hepatocyte growth factor receptor (tyrosine-protein kinase Met), vascular endothelial growth factor receptor 2 (VEGFR-2) and proto-oncogene tyrosine-protein kinase receptor Ret. There is ample evidence of Met, VEGFR-2 and Ret signaling in several tumor types. Preclinical data suggest that XL-184 has activity in tumors derived from both epithelial and mesenchymal origins. Phase I and II clinical studies support significant antitumor activity, particularly in medullary thyroid cancer and cancers metastatic to the bone. This review will evaluate XL-184's preclinical pharmacology, pharmacokinetics, drug interactions and clinical activity in phase I through phase III studies.

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来源期刊
Drugs of today
Drugs of today 医学-药学
CiteScore
3.90
自引率
0.00%
发文量
48
审稿时长
6-12 weeks
期刊介绍: An international, peer-reviewed journal publishing monographs on new products entering the market and review articles. Since its inception in 1965, Drugs of Today has established a reputation for excellence in providing physicians and other key healthcare professionals with practical, up-to-date monographs on recently approved and launched drugs.
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