首页> 外文期刊>Anticancer Research: International Journal of Cancer Research and Treatment >Previous Immune Checkpoint Inhibitor Treatment to Increase the Efficacy of Docetaxel and Ramucirumab Combination ChemotherapyPrevious Immune Checkpoint Inhibitor Treatment to Increase the Efficacy of Docetaxel and Ramucirumab Combination Chemotherapy
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Previous Immune Checkpoint Inhibitor Treatment to Increase the Efficacy of Docetaxel and Ramucirumab Combination ChemotherapyPrevious Immune Checkpoint Inhibitor Treatment to Increase the Efficacy of Docetaxel and Ramucirumab Combination Chemotherapy

机译:以往的免疫检查点抑制剂治疗,增加多西紫杉醇和拉姆梭拉组合组合化疗的疗效术治疗免疫检查点抑制剂治疗,增加了多西紫杉醇和拉姆索姆拉姆联合化疗的疗效

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Background/Aim: For immune checkpoint inhibitor (ICI)-pretreated patients, docetaxel and ramucirumab (DOC+RAM) combination therapy may be more effective compared to patients not receiving ICI treatment. Patients and Methods: From June 2013 to July 2018, 39 patients with advanced/recurrent non-small cell lung cancer underwent DOC+RAM therapy. We analyzed the efficacy and safety of DOC+RAM therapy based on the presence (pre-ICI+) or absence (pre-ICI-) of ICI pretreatment history. Results: Of the 39 patients treated with DOC+RAM, we identified 18 (46%) pre-ICI+ patients. Overall response rates for DOC+RAM concerning pre-ICI+ and pre-ICI- patients were 38.9% vs. 19.0%, respectively. Median progression-free survival (PFS) was 5.7 vs. 2.3 months [hazard ratio(HR)= 0.36; 95% confidence interval (CI)= 0.16-0.80]. Adverse events such as fever, myalgia, arthritis, pleural effusion, and pneumonitis tended to be increased in pre-ICI+ patients. Conclusion: Despite increased toxicity concerns, DOC+RAM therapy in pre-ICI+ patients showed a trend for tumor regression improvement and statistically significant prolongation of PFS.
机译:背景/目的:对于免疫检查点抑制剂(ICI) - 与未接受ICI治疗的患者相比,Docetaxel和Ramucirumab(Doc + Ram)组合治疗可能更有效。患者及方法:2013年6月至2018年7月,39例先进/复发性非小细胞肺癌接受了DOC + RAM治疗。我们根据ICI预处理历史的存在(预ICI +)或缺席(前ICI-)的存在,分析了DOC + RAM治疗的疗效和安全性。结果:39例患有Doc + RAM治疗的39名患者,我们确定了18例(46%)前ICI +患者。关于预诊所+和ICI-患者的DOC + RAM的总回应率分别为38.9%,分别为19.0%。中位进展生存期(PFS)为5.7与2.3个月[危险比(HR)= 0.36; 95%置信区间(CI)= 0.16-0.80]。发烧,肌痛,关节炎,胸膜积液和肺炎等不良事件往往在患有前ICI +患者中增加。结论:尽管有毒性较高,但在ICI +患者的Doc + Ram治疗表现出肿瘤回归改善的趋势,并统计上显着的PFS延长。

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