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首页> 外文期刊>Journal of Clinical Oncology >Gefitinib versus vinorelbine in chemotherapy-naive elderly patients with advanced non-small-cell lung cancer (INVITE): a randomized, phase II study.
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Gefitinib versus vinorelbine in chemotherapy-naive elderly patients with advanced non-small-cell lung cancer (INVITE): a randomized, phase II study.

机译:吉非替尼与长春瑞滨联合治疗的初次化疗的老年晚期非小细胞肺癌老年患者(INVITE):一项随机II期研究。

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PURPOSE: This phase II, open-label, parallel-group study compared gefitinib with vinorelbine in chemotherapy-naive elderly patients with advanced non-small-cell lung cancer (NSCLC). METHODS: Chemotherapy-naive patients (age >or= 70 years) were randomly assigned to gefitinib (250 mg/d orally) or vinorelbine (30 mg/m(2) infusion on days 1 and 8 of a 21-day cycle). The primary end point was progression-free survival (PFS). Secondary end points were overall survival (OS), objective response rate (ORR), quality of life (QOL), pulmonary symptom improvement (PSI), and tolerability. Exploratory end points included epidermal growth factor receptor (EGFR) gene copy number by fluorescent in situ hybridization (FISH). RESULTS: Patients were randomly assigned to gefitinib (n = 97) or to vinorelbine (n = 99). Hazard ratios (HR; gefitinib v vinorelbine) were 1.19 (95% CI, 0.85 to 1.65) for PFS and 0.98 (95% CI, 0.66 to 1.47) for OS. ORR and disease control rates were 3.1% (95% CI, 0.6 to 8.8) and 43.3% (for gefitinib) and 5.1% (95% CI, 1.7 to 11.4) and 53.5% (for vinorelbine), respectively. Overall QOL improvement and PSI rates were 24.3% and 36.6% (for gefitinib) and 10.9% and 31.0% (for vinorelbine), respectively. In the 54 patients who were EGFR FISH-positive, HRs were 3.13 (95% CI, 1.45 to 6.76) for PFS and 2.88 (95% CI, 1.21 to 6.83) for OS. There were fewer treatment-related grade 3 to 5 adverse events with gefitinib (12.8%) than with vinorelbine (41.7%). CONCLUSION: There was no statistical difference between gefitinib and vinorelbine in efficacy in chemotherapy-naive, unselected elderly patients with advanced NSCLC, but there was better tolerability with gefitinib. Individuals who were EGFR FISH-positive benefited more from vinorelbine than from gefitinib; this unexpected finding requires further study.
机译:目的:该II期开放标签,平行组研究比较了吉非替尼和长春瑞滨在未接受化疗的老年晚期非小细胞肺癌(NSCLC)患者中的应用。方法:将未接受化疗的年龄≥70岁的患者随机分配给吉非替尼(口服250 mg / d)或长春瑞滨(长春瑞滨)(在21天周期的第1天和第8天输注30 mg / m(2))。主要终点是无进展生存期(PFS)。次要终点是总生存期(OS),客观缓解率(ORR),生活质量(QOL),肺部症状改善(PSI)和耐受性。探索性终点包括通过荧光原位杂交(FISH)的表皮生长因子受体(EGFR)基因拷贝数。结果:患者被随机分配至吉非替尼(n = 97)或长春瑞滨(n = 99)。 PFS的危险比(HR;吉非替尼v长春瑞滨)为1.19(95%CI,0.85至1.65)和OS为0.98(95%CI,0.66至1.47)。 ORR和疾病控制率分别为3.1%(95%CI,0.6-8.8)和43.3%(吉非替尼)和5.1%(95%CI,1.7-11.4)和53.5%(长春瑞滨)。总体QOL改善和PSI率分别为24.3%和36.6%(对于吉非替尼)和10.9%和31.0%(对于长春瑞滨)。在54例EGFR FISH阳性患者中,PFS的HRs为3.13(95%CI,1.45至6.76),OS的HRs为2.88(95%CI,1.21至6.83)。与吉非替尼(12.8%)相比,与长春瑞滨(41.7%)相比,与治疗相关的3至5级不良事件更少。结论:吉非替尼和长春瑞滨在未接受化疗的未选老年NSCLC老年患者中疗效无统计学差异,但吉非替尼具有更好的耐受性。 EGFR FISH阳性的个体从长春瑞滨获益大于吉非替尼。这一意外发现需要进一步研究。

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