首页> 外文期刊>Journal of Clinical Oncology >Phase III study comparing cisplatin plus gemcitabine with cisplatin plus pemetrexed in chemotherapy-naive patients with advanced-stage non-small-cell lung cancer.
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Phase III study comparing cisplatin plus gemcitabine with cisplatin plus pemetrexed in chemotherapy-naive patients with advanced-stage non-small-cell lung cancer.

机译:Ⅲ期研究在未接受化疗的晚期非小细胞肺癌患者中比较了顺铂联合吉西他滨与顺铂联合培美曲塞。

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PURPOSE: Cisplatin plus gemcitabine is a standard regimen for first-line treatment of advanced non-small-cell lung cancer (NSCLC). Phase II studies of pemetrexed plus platinum compounds have also shown activity in this setting. PATIENTS AND METHODS: This noninferiority, phase III, randomized study compared the overall survival between treatment arms using a fixed margin method (hazard ratio [HR] 1.176) in 1,725 chemotherapy-naive patients with stage IIIB or IV NSCLC and an Eastern Cooperative Oncology Group performance status of 0 to 1. Patients received cisplatin 75 mg/m(2) on day 1 and gemcitabine 1,250 mg/m(2) on days 1 and 8 (n = 863) or cisplatin 75 mg/m(2) and pemetrexed 500 mg/m(2) on day 1 (n = 862) every 3 weeks for up to six cycles. RESULTS: Overall survival for cisplatin/pemetrexed was noninferior to cisplatin/gemcitabine (median survival, 10.3 v 10.3 months, respectively; HR = 0.94; 95% CI, 0.84 to 1.05). Overall survival was statistically superior for cisplatin/pemetrexed versus cisplatin/gemcitabine in patients with adenocarcinoma (n = 847; 12.6 v 10.9 months, respectively) and large-cell carcinoma histology (n = 153; 10.4 v 6.7 months, respectively). In contrast, in patients with squamous cell histology, there was a significant improvement in survival with cisplatin/gemcitabine versus cisplatin/pemetrexed (n = 473; 10.8 v 9.4 months, respectively). For cisplatin/pemetrexed, rates of grade 3 or 4 neutropenia, anemia, and thrombocytopenia (P or= .001); febrile neutropenia (P = .002); and alopecia (P .001) were significantly lower, whereas grade 3 or 4 nausea (P = .004) was more common. CONCLUSION: In advanced NSCLC, cisplatin/pemetrexed provides similar efficacy with better tolerability and more convenient administration than cisplatin/gemcitabine. This is the first prospective phase III study in NSCLC to show survival differences based on histologic type.
机译:目的:顺铂加吉西他滨是一线治疗晚期非小细胞肺癌(NSCLC)的标准方案。培美曲塞加铂化合物的II期研究也显示了在这种情况下的活性。患者和方法:这项非劣效性,III期随机研究比较了使用固定余量法(危险比[HR] <1.176)对1,725例初治为IIIB或IV期NSCLC并接受东方合作肿瘤治疗的患者的治疗组之间的总生存率小组表现状态为0到1。患者在第1天接受顺铂75 mg / m(2),在第1和第8天接受吉西他滨1,250 mg / m(2)(n = 863)或顺铂75 mg / m(2)和培美曲塞在第1天(n = 862)每3周服用500 mg / m(2),最多六个周期。结果:顺铂/培美曲塞的总生存期不逊于顺铂/吉西他滨(中位生存期分别为10.3 v 10.3个月; HR = 0.94; 95%CI,0.84至1.05)。腺癌(n = 847;分别为12.6 v 10.9个月)和大细胞癌组织学检查(n = 153; 10.4 v 6.7个月)的患者,顺铂/培美曲塞的总生存率在统计学上优于顺铂/吉西他滨。相反,在鳞状细胞组织学患者中,顺铂/吉西他滨相对于顺铂/培美曲塞的生存率有显着改善(分别为473、10.8和9.4个月)。对于顺铂/培美曲塞,发生3或4级嗜中性白血球减少症,贫血和血小板减少症的比率(P <或= 0.001);发热性中性粒细胞减少症(P = .002);和脱发(P <.001)显着降低,而3级或4级恶心(P = .004)更常见。结论:在晚期非小细胞肺癌中,与顺铂/吉西他滨相比,顺铂/培美曲塞具有相似的疗效,更好的耐受性和更方便的给药。这是NSCLC中第一个前瞻性III期研究,显示了根据组织学类型的生存差异。

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