首页> 外文期刊>Annals of oncology: official journal of the European Society for Medical Oncology >Randomized phase II trial of weekly paclitaxel combined with carboplatin versus standard paclitaxel combined with carboplatin for elderly patients with advanced non-small-cell lung cancer.
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Randomized phase II trial of weekly paclitaxel combined with carboplatin versus standard paclitaxel combined with carboplatin for elderly patients with advanced non-small-cell lung cancer.

机译:每周紫杉醇联合卡铂与标准紫杉醇联合卡铂治疗老年晚期非小细胞肺癌的随机II期试验。

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BACKGROUND: The optimal platinum doublet regimen in elderly patients with non-small-cell lung cancer (NSCLC) is still uncertain. We conducted a randomized phase II study to compare the efficacy and safety of weekly paclitaxel combined with carboplatin with those of the standard schedule. PATIENTS AND METHODS: Elderly patients (age > or =70 years) with advanced NSCLC were randomly assigned to either the weekly arm {70 mg/m(2) paclitaxel on days 1, 8, and 15 and carboplatin [area under the curve (AUC) = 6] on day 1} or the standard arm [200 mg/m(2) paclitaxel and carboplatin (AUC = 6) on day 1]. The primary end point was the overall response rate (ORR). RESULTS: Eighty-two patients were enrolled. The ORR and median progression-free survival were 55% and 6.0 months for the weekly arm and 53% and 5.6 months for the standard arm. Grade 3/4 neutropenia and peripheral neuropathy were observed in 41% and 0% of the patients in the weekly arm and in 88% and 25% in the standard arm, respectively. CONCLUSIONS: This is the first randomized study that compares the platinum doublet designed specifically for the elderly. Regarding the safety, the weekly regimen was less toxic than the standard regimen and seems to be preferable for elderly patients with advanced NSCLC.
机译:背景:老年非小细胞肺癌(NSCLC)患者的最佳铂族双联方案尚不确定。我们进行了一项随机的II期研究,以比较每周紫杉醇联合卡铂与标准疗程的疗效和安全性。患者与方法:年龄≥70岁的晚期NSCLC老年患者被随机分配至第1、8、15天每周一次(70 mg / m(2)紫杉醇和卡铂[曲线下面积(第1天的AUC] = 6]或标准臂[第1天的200 mg / m(2)紫杉醇和卡铂(AUC = 6)]。主要终点是总体缓解率(ORR)。结果:82例患者入选。每周治疗组的ORR和中位无进展生存期分别为55%和6.0个月,标准治疗组为53%和5.6个月。每周组分别有41%和0%的患者观察到3/4级中性粒细胞减少和周围神经病变,在标准组中分别观察到了88%和25%。结论:这是第一项比较专门为老年人设计的铂金双联体的随机研究。关于安全性,每周方案比标准方案毒性小,对于晚期NSCLC的老年患者似乎更可取。

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