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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:雷戈非尼,顺铂和培美曲塞在晚期非鳞状非小细胞肺癌患者中的初步安全性,药代动力学和疗效

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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:瑞戈非尼是一种具有有效抗血管生成活性的口服多靶点激酶抑制剂。在这一阶段的I期试验中,我们评估了雷戈非尼联合顺铂和培美曲塞对晚期非鳞状非小细胞肺癌(nsNSCLCs)患者的安全性,药代动力学和疗效。 9名患者在研究提前终止前入组。 9名患者中有5名(56%)有部分缓解,中位无进展生存期为7个月(范围1.5-15.1个月)。在晚期nsNSCLC患者中,Regorafenib与标准剂量的顺铂和培美曲塞合用具有可接受的耐受性和较小的药代动力学相互作用。

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