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首页> 外文期刊>Japanese journal of clinical oncology. >Osimertinib versus standard-of-care EGFR-TKI as first-line treatment for EGFRm advanced NSCLC: FLAURA Japanese subset
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Osimertinib versus standard-of-care EGFR-TKI as first-line treatment for EGFRm advanced NSCLC: FLAURA Japanese subset

机译:Osimertinib与护理标准EGFR-TKI作为EGFRM高级NSCLC的一线治疗:Flaura日本子集

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Background: The FLAURA study was a multicenter, double-blind, Phase 3 study in which patients with previously untreated epidermal growth factor receptor mutation-positive advanced non-small-cell lung carcinoma were randomized 1:1 to oral osimertinib 80 mg once daily or standard-of-care (gefitinib 250 mg or erlotinib 150 mg, once daily) to compare safety and efficacy. In the overall FLAURA study, significantly better progression-free survival was shown with osimertinib versus standard-of-care. Methods: Selected endpoints, including progression-free survival (primary endpoint), overall survival, objective response rate, duration of response and safety were evaluated for the Japanese subset of the FLAURA study. Results: In Japan, 120 eligible Japanese patients were randomized to osimertinib (65 patients) or gefitinib (55 patients) treatment from December 2014 to June 2017. Median progression-free survival was 19.1 (95% confidence interval, 12.6, 23.5) and 13.8 (95% confidence interval, 8.3, 16.6) months with osimertinib and gefitinib, respectively (hazard ratio, 0.61; 95% confidence interval, 0.38, 0.99). Median overall survival was not reached in either treatment arm (data were immature). In the osimertinib and gefitinib arms, objective response rate was 75.4% (49/65) and 76.4% (42/55), and median duration of response from onset was 18.4 (95% confidence interval, not calculated) and 9.5 (95% confidence interval, 6.2, 13.9) months, respectively. The incidence of adverse events was similar in the two groups. The frequency of Grade >=3 interstitial lung disease and pneumon-itis in the two groups were the same (one patient). Conclusions: As the first-line therapy, osimertinib showed significantly improved efficacy versus gefitinib in the Japanese population of the FLAURA study. No new safety concerns were raised. Clinical trial registration: NCT02296125 (ClinicalTrials.gov)
机译:背景:Flaura研究是一种多中心,双盲,相3研究,其中具有以前未经治疗的表皮生长因子受体突变阳性阳性的未小细胞肺癌的患者将每天一次或每天一次进行一次Oral Osimertinib 80 mg护理标准(GEFITINIB 250 mg或erlotinib 150 mg,每日一次)以比较安全性和功效。在整个浮游生研究中,通过Osimertinib与护理标准显示出明显更好的进展存活。方法:对日本佛拉巴研究的日本子集评估所选终点,包括无进展存活(主要终点),总体存活,客观响应率,响应持续时间和安全。结果:在日本,120名符合条件的日本患者于2014年12月至2017年6月随机转移到Osimertinib(65名患者)或Gefitinib(55名患者)治疗。中位进展生存率为19.1(95%置信区间,12.6,23.5)和13.8 (分别与Osimertinib和Gefitinib的95%置信区间,8.3,16.6)个月(危险比,0.61; 95%置信区间,0.38,0.99)。在任何一种治疗臂(数据不成熟)中都没有达到中位数的整体存活。在Osimertinib和Gefitinib武器中,客观反应率为75.4%(49/65)和76.4%(42/55),发病的中值持续时间为18.4(95%置信区间,未计算)和9.5(95%)(95%)(95%分别置信区间,6.2,13.9)个月。两组不良事件的发生率类似。等级的频率> = 3间质肺病和两组中的肺炎 - ITIS是相同的(一个患者)。结论:作为一线治疗,Osimertinib在普拉拉研究中日本人口中的吉维替尼显示出显着提高。没有提出新的安全问题。临床试验注册:NCT02296125(ClinicalTrials.gov)

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