首页> 外文期刊>Oncology research and treatment. >Necitumumab plus Gemcitabine and Cisplatin as First-Line Therapy in Patients with Stage IV EGFR-Expressing Squamous Non-Small-Cell Lung Cancer German Subgroup Data from an Open-Label, Randomized Controlled Phase 3 Study (SQUIRE)
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Necitumumab plus Gemcitabine and Cisplatin as First-Line Therapy in Patients with Stage IV EGFR-Expressing Squamous Non-Small-Cell Lung Cancer German Subgroup Data from an Open-Label, Randomized Controlled Phase 3 Study (SQUIRE)

机译:奈瑟单抗+吉西他滨和顺铂作为IV期表达EGFR鳞状非小细胞肺癌患者的一线治疗德国亚组数据来自开放标签,随机对照3期研究(SQUIRE)

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Background: In the SQUIRE study, adding the anti epidermal growth factor receptor (EGFR) IgG1 antibody necitumumab to first-line gemcitabine and cisplatin (GC + N) in advanced squamous non-small-cell lung cancer (sqNSCLC) significantly improved overall survival (OS); the safety profile was acceptable. We explored data for the German subpopulation (N = 96) of SQUIRE patients with EGFR-expressing tumors. Patient and Methods: Patients with stage IV sqNSCLC were randomized 1:1 to up to 6 cycles of open-label GC + N or GC alone. GC + N patients with no progression continued on necitumumab monotherapy until disease progression or intolerable toxicity. The primary endpoint was OS; thesecondary endpoints included progression-free survival (PFS), safety and health-related quality of life (EQ-5D, Lung Cancer Symptom Scale (LOSS)). Results: The 96 German SQUIRE patients with EGFR-expressing tumors (GC + N 42, GC 54) received a median of 4 GC cycles; the GC + N patients received 5 cycles of necitumumab. Adding necitumumab was associated with 41% risk reduction of death (hazard ratio (HR) 0.59, 95% confidence interval (CI) 0.37-0.94, p = 0.026) and 44% risk reduction of progression (HR 0.56, 95% CI 0.33-0.95, p = 0.029). Adverse events typically associated with EGFR antibody treatment (including rash, hypomagnesemia) were more common with GC + N. The time to deterioration of the EQ-5D and LOSS scores showed no notable differences between the treatment arms, except for appetite loss (delayed for GC + N). Conclusion: The survival benefit from adding necitumumab to first-line GC was more pronounced in the German SQUIRE subpopulation with EGFR-expressing tumors than in the overall (intention-to-treat) population; toxicity was manageable and consistent with the overall population. (C) 2016 S. Karger GmbH, Freiburg
机译:背景:在SQUIRE研究中,将抗表皮生长因子受体(EGFR)IgG1抗体necitumumab加入一线吉西他滨和顺铂(GC + N)一线治疗晚期鳞状非小细胞肺癌(sqNSCLC)中,可显着改善总体生存率(操作系统);安全性是可以接受的。我们探索了SQUIRE表达EGFR肿瘤患者的德国亚人群(N = 96)的数据。患者和方法:将IV期sqNSCLC阶段的患者1:1随机分配到开放标记GC + N或单独使用GC的多达6个周期。没有进展的GC + N患者继续接受尼妥珠单抗单药治疗,直到疾病进展或无法忍受的毒性反应为止。主要终点是操作系统;次要终点包括无进展生存期(PFS),与安全和健康有关的生活质量(EQ-5D,肺癌症状量表(LOSS))。结果:96名患有EGFR表达肿瘤(GC + N 42,GC 54)的德国SQUIRE患者接受了4个GC周期的中位治疗。 GC + N患者接受了5个疗程的尼妥单抗治疗。加入尼西珠单抗可降低41%的死亡风险(危险比(HR)0.59,95%的置信区间(CI)0.37-0.94,p = 0.026)和44%的进展风险降低(HR 0.56,95%CI 0.33- 0.95,p = 0.029)。 GC + N较常发生与EGFR抗体治疗相关的不良事件(包括皮疹,低镁血症)。EQ-5D和LOSS评分恶化的时间表明治疗组之间无显着差异,除了食欲减退(延迟GC + N)。结论:在表达EGFR的肿瘤的德国SQUIRE亚人群中,在一线GC中加入奈珠单抗的生存获益比总的(意图治疗)人群更为明显。毒性是可控的并且与总人口一致。 (C)2016 S.Karger GmbH,弗赖堡

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