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首页> 外文期刊>British Journal of Cancer >Impact of KRAS codon subtypes from a randomised phase II trial of selumetinib plus docetaxel in KRAS mutant advanced non-small-cell lung cancer
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Impact of KRAS codon subtypes from a randomised phase II trial of selumetinib plus docetaxel in KRAS mutant advanced non-small-cell lung cancer

机译:selumetinib + docetaxelⅡ期随机试验对KRAS密码子亚型在 KRAS 突变晚期非小细胞肺癌中的作用

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Background: Selumetinib (AZD6244, ARRY-142886)+docetaxel increases median overall survival (OS) and significantly improves progression-free survival (PFS) and objective response rate (ORR) compared with docetaxel alone in patients with KRAS mutant, stage IIIB/IV non-small-cell lung cancer (NSCLC; NCT00890825). Methods: Retrospective analysis of OS, PFS, ORR and change in tumour size at week 6 for different sub-populations of KRAS codon mutations. Results: In patients receiving selumetinib+docetaxel and harbouring KRAS G12C or G12V mutations there were trends towards greater improvement in OS, PFS and ORR compared with other KRAS mutations. Conclusion: Different KRAS mutations in NSCLC may influence selumetinib/docetaxel sensitivity.
机译:背景:与单独使用多西他赛的KRAS突变患者(IIIB / IV期)相比,Selumetinib(AZD6244,ARRY-142886)+多西他赛可提高中位总体生存率(OS),并显着改善无进展生存期(PFS)和客观缓解率(ORR)。非小细胞肺癌(NSCLC; NCT00890825)。方法:回顾性分析第6周的不同KRAS密码子突变亚群的OS,PFS,ORR和肿瘤大小的变化。结果:与其他KRAS突变相比,接受selumetinib +多西他赛治疗且具有KRAS G12C或G12V突变的患者OS,PFS和ORR的改善趋势更大。结论:NSCLC中不同的KRAS突变可能影响selumetinib /多西他赛敏感性。

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