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首页> 外文期刊>Lung cancer: Journal of the International Association for the Study of Lung Cancer >Dose-escalation study of pemetrexed in combination with carboplatin followed by pemetrexed maintenance therapy for advanced non-small cell lung cancer.
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Dose-escalation study of pemetrexed in combination with carboplatin followed by pemetrexed maintenance therapy for advanced non-small cell lung cancer.

机译:培美曲塞联合卡铂联合培美曲塞维持治疗用于晚期非小细胞肺癌的剂量递增研究。

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INTRODUCTION: The primary objectives of this study were to determine the recommended dose of pemetrexed and carboplatin in patients with chemo-naive advanced non-small cell lung cancer (NSCLC). METHODS: Patients received escalated doses of carboplatin area under the concentration-time curve (AUC) of 5 (cohort 1) or 6 (cohort 2) and pemetrexed 500 mg/m(2) every 3 weeks for six cycles. For patients with objective response and stable disease, pemetrexed were continued until disease progression or unacceptable toxicity. RESULTS: In cohort 1, a dose-limiting toxicity (DLT) was observed in one of the six patients: grade 4 thrombocytopenia. No DLTs were seen in the first 6 patients of cohort 2, and thus the combination of pemetrexed 500 mg/m(2) plus carboplatin at AUC 6 was determined as the recommended dose. Among a total of 20 patients, 8 patients received a median of four cycles of pemetrexed monotherapy in a maintenance setting without unexpected or cumulative toxicities. No complete responses and 12 partial responses were observed, giving an overall response rate of 60.0% [95% confidence interval (CI), 36.1-80.9%]. Median progression-free survival time for all patients was 7.6 months (95% CI: 4.8-8.0 months). CONCLUSIONS: Pemetrexed 500 mg/m(2) plus carboplatin AUC 6 combination therapy followed by pemetrexed maintenance therapy, is generally tolerable, and shows encouraging antitumor activity in chemotherapy-naive patients with advanced NSCLC.
机译:简介:本研究的主要目的是确定未接受化学治疗的晚期非小细胞肺癌(NSCLC)患者的培美曲塞和卡铂的推荐剂量。方法:患者在浓度-时间曲线(AUC)为5(组1)或6(组2)的浓度-时间曲线下(AUC)递增剂量,每3周培美曲塞500 mg / m(2),共六个周期。对于具有客观反应和疾病稳定的患者,继续使用培美曲塞直至疾病进展或出现不可接受的毒性。结果:在队列1中,在六名患者之一中观察到剂量限制性毒性(DLT):4级血小板减少。在队列2的前6名患者中未观察到DLT,因此将培美曲塞500 mg / m(2)加卡铂在AUC 6的组合确定为推荐剂量。在总共20例患者中,有8例患者在维持环境中接受了培美曲塞单药治疗四个周期的中位数,而没有意外或累积的毒性。没有观察到完全缓解和12个部分缓解,总体缓解率为60.0%[95%置信区间(CI),36.1-80.9%]。所有患者的无进展生存时间中位数为7.6个月(95%CI:4.8-8.0个月)。结论:培美曲塞500 mg / m(2)加上卡铂AUC 6联合治疗后再进行培美曲塞维持治疗,通常是可以耐受的,并且对未接受过化疗的初发NSCLC患者显示出令人鼓舞的抗肿瘤活性。

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