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首页> 外文期刊>Lung cancer: Journal of the International Association for the Study of Lung Cancer >A phase I/II study of carboplatin plus gemcitabine for elderly patients with advanced non-small cell lung cancer: West Japan Thoracic Oncology Group Trial (WJTOG) 2905
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A phase I/II study of carboplatin plus gemcitabine for elderly patients with advanced non-small cell lung cancer: West Japan Thoracic Oncology Group Trial (WJTOG) 2905

机译:卡铂联合吉西他滨治疗老年晚期非小细胞肺癌的I / II期研究:西日本胸腔肿瘤小组试验(WJTOG)2905

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Introduction: Monotherapy with a third generation anticancer agent has been regarded as the standard therapy for elderly patients with advanced non-small-cell lung cancer (NSCLC). However, it is unclear whether elderly patients with a good performance status can tolerate platinum-doublet chemotherapy like younger patients. Methods: A combination phase I/II study was conducted in chemo-naive elderly patients with NSCLC to establish the toxicity and maximum tolerated dose (MTD) and to investigate the antitumor activity of carboplatin (CBDCA) plus gemcitabine (GEM). GEM was infused on days 1 and 8, and CBDCA on day 1 every 3. weeks. Results: Seventy-five patients were enrolled. The most frequent toxicities were hematological, especially thrombocytopenia. Three of three patients experienced a dose-limiting toxicity at dose level 3: 1000mg/m 2 GEM with AUC 5 CBDCA (MTD), and one of seven patients at level 2a: 1000mg/m 2 GEM with AUC 4 CBDCA (recommended dose). In the phase II study, the overall response rate was 22.2% and the median overall survival time was 14.2months. Conclusions: Although the recommended dosage is restricted to a lower level compared to younger patients, combination therapy using CBDCA with GEM is tolerable and promising for elderly patients with advanced NSCLC.
机译:简介:第三代抗癌药的单一疗法已被视为老年晚期非小细胞肺癌(NSCLC)患者的标准疗法。但是,尚不清楚性能良好的老年患者是否可以像年轻患者一样耐受铂类双联化疗。方法:对未经化疗的老年NSCLC患者进行I / II期联合研究,以确定毒性和最大耐受剂量(MTD)并研究卡铂(CBDCA)加吉西他滨(GEM)的抗肿瘤活性。每3周在第1天和第8天注入GEM,在第1天注入CBDCA。结果:75例患者入组。最常见的毒性是血液学毒性,尤其是血小板减少症。三分之三的患者在剂量水平3时出现剂量限制性毒性:AUC 5 CBDCA(MTD)为1000mg / m 2 GEM,七分之二a的患者之一:AUC 4 CBDCA的剂量为1000mg / m 2 GEM(推荐剂量) 。在II期研究中,总缓解率为22.2%,中位总生存时间为14.2个月。结论:尽管与年轻患者相比,推荐剂量被限制在较低水平,但CBDCA与GEM的联合治疗对晚期NSCLC的老年患者是可以忍受的,并且很有希望。

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