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首页> 外文期刊>Lung cancer: Journal of the International Association for the Study of Lung Cancer >Sequential administration of docetaxel followed by maintenance gefitinib, as salvage treatment in patients with advanced NSCLC: a multicenter phase II trial.
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Sequential administration of docetaxel followed by maintenance gefitinib, as salvage treatment in patients with advanced NSCLC: a multicenter phase II trial.

机译:多西紫杉醇的序贯给药,继之以吉非替尼维持治疗,作为晚期NSCLC患者的挽救性治疗:一项多中心II期试验。

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PURPOSE: To evaluate the activity and toxicity of the sequential administration of docetaxel followed by gefitinib in patients with advanced non-small cell lung cancer (NSCLC). PATIENTS AND TREATMENT: Forty-one patients pre-treated with at least one prior chemotherapy regimen (platinum- or taxane-based) for advanced/metastatic NSCLC received three cycles of docetaxel 30 mg/m2, administered as a 1-h IV infusion, on days 1, 8 and 15 of each 4-week cycle followed by gefitinib 250 mg daily po. Gefitinib treatment was continued until disease progression, development of unacceptable toxicity, or withdrawal of patients consent. RESULTS: Two (4.9%) patients achieved a partial response and 10 (24.4%) stable disease, for a disease control rate of 29.3% (95% CI: 15.3%-43.2%) while on weekly docetaxel treatment. Additionally, progressive disease (PD) was observed in 29 (70.7%). No objective responses were observed during the gefitinib maintenance therapy; however, 17 (41.5%) patients presented stable disease maintained for more than 2 months. Median time to progression was 3.0 months (range: 1-38.3 months; 95% CI: 2.4-3.6); median overall survival 6.9 months (range: 1.2-40.2 months; 95% CI: 5.34-8.52) while the 1-year survival was 28.8%. Therapy was generally well tolerated with diarrhea and rash being the most frequent toxicities. CONCLUSIONS: The sequential administration of docetaxel and gefitinib was well tolerated and moderately active against advanced pre-treated NSCLC.
机译:目的:评估先后服用多西他赛和吉非替尼对晚期非小细胞肺癌(NSCLC)患者的活性和毒性。病人和治疗:41位接受过至少一种先前的晚期/转移性NSCLC化疗方案(铂或紫杉类为基础)的患者接受了多西紫杉醇30 mg / m2的三个周期的治疗,每次1小时静脉输注,在每个4周周期的第1、8和15天服用吉非替尼,每日口服250 mg。吉非替尼治疗一直持续到疾病进展,出现无法接受的毒性反应或患者同意退出治疗。结果:接受多西他赛治疗的患者中,有2名(4.9%)患者获得了部分缓解和10名(24.4%)稳定的疾病,疾病控制率为29.3%(95%CI:15.3%-43.2%)。此外,在29(70.7%)中观察到进行性疾病(PD)。吉非替尼维持治疗期间未观察到客观反应;但是,有17名(41.5%)的患者病情稳定了2个月以上。中位进展时间为3.0个月(范围:1-38.3个月; 95%CI:2.4-3.6);中位总体生存期为6.9个月(范围:1.2-40.2个月; 95%可信区间:5.34-8.52),而一年生存率为28.8%。通常对治疗的耐受性良好,腹泻和皮疹是最常见的毒性反应。结论:多西他赛和吉非替尼序贯给药对晚期NSCLC具有良好的耐受性和中等活性。

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