首页> 外文期刊>Lung cancer: Journal of the International Association for the Study of Lung Cancer >Biweekly combination therapy with gemcitabine and carboplatin compared with gemcitabine monotherapy in elderly patients with advanced non-small-cell lung cancer: A randomized, phase-II study
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Biweekly combination therapy with gemcitabine and carboplatin compared with gemcitabine monotherapy in elderly patients with advanced non-small-cell lung cancer: A randomized, phase-II study

机译:与吉西他滨单药治疗相比,吉西他滨和卡铂双周联合治疗老年晚期非小细胞肺癌患者:II期随机研究

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Introduction: The strategy of chemotherapy in the elderly is controversial. We wanted to evaluate the efficacy and safety of biweekly gemcitabine and low-dose carboplatin combination therapy in elderly patients with advanced non-small-cell lung cancer (NSCLC). Methods: In this phase-II trial, chemotherapy-naive elderly patients (aged ≥76 years) with NSCLC were randomly treated with biweekly combination therapy with gemcitabine and carboplatin (1000mg/m 2 gemcitabine and carboplatin at an area under the curve (AUC) of 3 on days 1 and 15, every 4 weeks) or gemcitabine monotherapy (1000mg/m 2 on days 1, 8 and 15, every 4 weeks). The primary endpoint was overall response rate and analysis was based on intention-to-treat. Results: Thirty-one patients were randomly assigned combination therapy and 30 were assigned monotherapy. The median age was 79.0 years. Response rate was 22.6% (95% confidence interval (CI): 11.4-39.8%) for biweekly combination therapy and 10.0% (95% CI: 3.5-25.6%) for monotherapy. Median progression-free survival in combination chemotherapy was 3.9 months (95% CI: 0.5-8.5 months), which was significantly longer that that in monotherapy (2.4 months, 95% CI: 0.5-6.7 months). The prevalence of hematological and non-hematological adverse events reaching grade 3/4 was not significantly different between combination therapy and monotherapy. Conclusions: Biweekly gemcitabine and low-dose carboplatin combination chemotherapy showed acceptable efficacy, toxicity, and tolerability in those aged ≥76 years with NSCLC. Further investigations with a large population are required to confirm our results.
机译:简介:老年人的化疗策略存在争议。我们希望评估吉西他滨和小剂量卡铂联合治疗对老年晚期非小细胞肺癌(NSCLC)老年患者的疗效和安全性。方法:在此II期临床试验中,对未接受化疗的NSCLC老年患者(年龄≥76岁)随机接受吉西他滨和卡铂(1000mg / m 2吉西他滨和卡铂在曲线下面积(AUC))每两周联合治疗在第1天和第15天每3周服用3次)或吉西他滨单药治疗(第4天,第8天和第15天在1000mg / m 2)。主要终点为总体反应率,分析基于意向治疗。结果:31例患者被随机分配联合治疗,30例被分配单一治疗。中位年龄是79.0岁。双周联合疗法的缓解率为22.6%(95%置信区间(CI):11.4-39.8%),单药疗法为10.0%(95%CI:3.5-25.6%)。联合化疗的中位无进展生存期为3.9个月(95%CI:0.5-8.5个月),比单药治疗(2.4个月,95%CI:0.5-6.7个月)明显更长。联合疗法和单一疗法之间血液学和非血液学不良事件的发生率达到3/4级没有显着差异。结论:吉西他滨和低剂量卡铂联合化疗每两周一次,在≥76岁的NSCLC患者中显示出可接受的疗效,毒性和耐受性。需要进一步的大量调查以确认我们的结果。

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