Porta Camillo, Giglione Palma, Liguigli Wanda, Paglino Chiara
Medical Oncology, IRCCS San Matteo University Hospital Foundation, Piazzale C Golgi, 19, 27100 Pavia, Italy.
Future Oncol. 2015;11(1):39-50. doi: 10.2217/fon.14.208.
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.
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。