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首页> 外文期刊>Clinical lung cancer >Preliminary Safety, Pharmacokinetics, and Efficacy of Regorafenib, Cisplatin, and Pemetrexed in Patients With Advanced Nonsquamous Non-Small-Cell Lung Cancers
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Preliminary Safety, Pharmacokinetics, and Efficacy of Regorafenib, Cisplatin, and Pemetrexed in Patients With Advanced Nonsquamous Non-Small-Cell Lung Cancers

机译:高级非小细胞肺癌患者术初步安全性,药代动力学和疗效,顺铂和培养基患者

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摘要

Regorafenib is an oral multitargeted kinase inhibitor with potent antiangiogenic activity. In this phase I trial we evaluated the safety, pharmacokinetics, and efficacy of regorafenib with cisplatin and pemetrexed for patients with advanced nonsquamous non-small-cell lung cancers (nsNSCLCs). Nine patients enrolled before premature termination of the study. Five of 9 (56%) patients had a partial response and the median progressionfree survival was 7 months (range, 1.5-15.1 months). Regorafenib had acceptable tolerability and minor pharmacokinetic interactions in combination with standard doses of cisplatin and pemetrexed in patients with advanced nsNSCLCs.
机译:Regorafenib是一种口服型抗血管生成活性的口腔型激酶抑制剂。 在该阶段,我试验我们评估了Regorafenib与顺铂的安全性,药代动力学和疗效,并针对先进的非小细胞肺癌患者(NSNSCLC)的患者。 九名患者在研究过早终止之前注册。 9名(56%)患者中的五种患者的部分反应,中位进展脱脂生存率为7个月(范围,1.5-15.1个月)。 Regorafenib在高级NSNSCLC患者中具有可接受的可耐受性和较小的药代动力学相互作用和患有标准剂量的顺铂和培养基。

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