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首页> 外文期刊>Annals of oncology: official journal of the European Society for Medical Oncology >A phase I, dose-escalation study of volasertib combined with nintedanib in advanced solid tumors
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A phase I, dose-escalation study of volasertib combined with nintedanib in advanced solid tumors

机译:晚期实体瘤中伏拉塞替尼与尼达尼布联合应用的I期剂量递增研究

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摘要

This phase I trial determined that the Polo-like kinase inhibitor volasertib can be combined at the recommended single-agent dose (300 mg every 3 weeks) with nintedanib (200 mg twice a day), a triple angiokinase inhibitor, in patients with advanced solid tumors. Combination treatment demonstrated antitumor activity and a generally manageable safety profile.Volasertib is a potent and selective cell-cycle kinase inhibitor that induces mitotic arrest and apoptosis by targeting Polo-like kinases. This study determined the maximum tolerated dose (MTD) and pharmacokinetics of volasertib combined with nintedanib, a potent and orally bioavailable triple angiokinase inhibitor, in patients with advanced solid tumors.
机译:这项I期临床试验确定,对于晚期固体患者,Polo样激酶抑制剂伏拉塞替尼可以以推荐的单药剂量(每3周300毫克)与nintedanib(每天两次,200毫克)三联血管激酶抑制剂联合使用。肿瘤。联合治疗显示出抗肿瘤活性和通常可控的安全性。Volasertib是一种有效的选择性细胞周期激酶抑制剂,可通过靶向Polo样激酶诱导有丝分裂阻滞和细胞凋亡。这项研究确定了晚期实体瘤患者中,沃拉塞替尼与一种有效且口服可生物利用的三联血管激酶抑制剂nintedanib联合使用的最大耐受剂量(MTD)和药代动力学。

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