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多韦替尼(CHIR258,TKI258):结构、研发以及临床前和临床活性

Dovitinib (CHIR258, TKI258): structure, development and preclinical and clinical activity.

作者信息

Porta Camillo, Giglione Palma, Liguigli Wanda, Paglino Chiara

机构信息

Medical Oncology, IRCCS San Matteo University Hospital Foundation, Piazzale C Golgi, 19, 27100 Pavia, Italy.

出版信息

Future Oncol. 2015;11(1):39-50. doi: 10.2217/fon.14.208.

Abstract

Dovitinib is an oral multikinase inhibitor targeting FGF receptors, PDGF receptors and VEGF receptors. Its activity against FGF receptors suggests its usefulness in treating cancers after the failure of VEGF/VEGF receptor-targeting agents. The identified dose and schedule to be used in further studies was 500 mg orally for 5 days on and 2 days off. Biological considerations and the results achieved in a Phase I/II trial suggested its activity in advanced renal cell carcinoma patients pretreated with a tyrosine kinase inhibitor and an mTOR inhibitor. Surprisingly, in a randomized controlled Phase III trial versus sorafenib in the same setting, dovitinib failed to demonstrate any superiority. At present, dovitinib is being tested in different tumor types. However, molecular-based patient selection seems to be key to fully exploit the activity of this drug.

摘要

多韦替尼是一种口服多激酶抑制剂,可靶向成纤维细胞生长因子(FGF)受体、血小板衍生生长因子(PDGF)受体和血管内皮生长因子(VEGF)受体。其对FGF受体的活性表明,在VEGF/VEGF受体靶向药物治疗失败后,它可用于治疗癌症。进一步研究确定的使用剂量和方案为口服500毫克,连续服用5天,停药2天。生物学考量以及一项I/II期试验的结果表明,它对先前接受过酪氨酸激酶抑制剂和mTOR抑制剂治疗的晚期肾细胞癌患者具有活性。令人惊讶的是,在相同背景下与索拉非尼进行的一项随机对照III期试验中,多韦替尼未能显示出任何优势。目前,多韦替尼正在不同肿瘤类型中进行测试。然而,基于分子的患者选择似乎是充分发挥该药物活性的关键。

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