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Afatinib in locally advanced/metastatic NSCLC harboring common EGFR mutations, after chemotherapy: a Phase IV study

机译:化疗后局部晚期/转移性NSCLC中具有常见EGFR突变的阿法替尼:一项IV期研究

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Aim: The current study evaluated the efficacy and tolerability of second-line afatinib in patients with EGFR mutation-positive (EGFRm+) non-small-cell lung cancer (NSCLC) following chemotherapy. Patients & methods: In this open-label, single-arm Phase IV study, patients with EGFRm+ (Del19/L858R) NSCLC who had progressed following platinum-based chemotherapy received afatinib (starting dose 40?mg/day). The primary end point was confirmed objective response. Results: 60 patients received afatinib for a median duration of 11.5 months. 50% of patients had a confirmed objective response, of median duration 13.8 months. Median progression-free survival was 10.9 months. The most common treatment-related adverse events were diarrhea (72%), rash (28%) and paronychia (23%). Conclusion: Our data support the use of afatinib (40?mg/day) as an effective and well-tolerated second-line treatment in EGFRm+ NSCLC.
机译:目的:本研究评估了二线阿法替尼对化疗后EGFR突变阳性(EGFRm +)非小细胞肺癌(NSCLC)患者的疗效和耐受性。患者与方法:在这项开放性单臂IV期研究中,铂类化疗后进展的EGFRm +(Del19 / L858R)NSCLC患者接受阿法替尼治疗(起始剂量为40?mg /天)。主要终点被确认为客观反应。结果:60名患者接受阿法替尼治疗,中位持续时间为11.5个月。 50%的患者确诊为客观反应,中位持续时间为13.8个月。中位无进展生存期为10.9个月。与治疗相关的最常见不良事件为腹泻(72%),皮疹(28%)和甲沟炎(23%)。结论:我们的数据支持使用阿法替尼(40?mg /天)作为EGFRm + NSCLC的有效且耐受良好的二线治疗。

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