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Combination therapy with docetaxel and low dose of cisplatin in elderly patients with advanced non-small cell lung cancer: multicenter phase II study.

机译:多西他赛和低剂量顺铂联合治疗老年晚期非小细胞肺癌患者:多中心II期研究。

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摘要

PURPOSE: To determine the efficacy and safety of the combination therapy with docetaxel and cisplatin (CDDP) at low doses in elderly patients with advanced NSCLC. PATIENTS AND METHODS: A total of 42 patients aged > or =70 years with previously untreated advanced NSCLC received docetaxel 75 mg/m(2) plus CDDP 50 mg/m(2) on day 1. The regimen was repeated every 21 days. Patients received a minimum of three courses unless progressive disease was detected. RESULTS: By intent-to-treat analysis, the overall response rate was 31% (95% CI, 17.8-47.2%). A total of 18 patients (43%) had stable disease and 11 (26%) progressed. Median time to progression was 5.2 months. Overall median survival was 8.9 months, with 1-year actuarial survival rate of 41%. Eastern Cooperative Oncology Group performance status was improved in 18 patients (43%). The chemotherapy regimen was well tolerated. A total of 11 patients (26%) had grade 3/4 adverse events: 7 (17%) neutropenia (one of them was diagnosed with febrile neutropenia), 3 (7%) asthenia, 3 (7%) nausea/vomiting, 1 (2%) diarrhea, 1 (2%) thrombocytopenia and 1 (2%) neurotoxicity. No death due to toxicity was seen. CONCLUSION: The combination of low-dose CDDP and docetaxel for elderly patients with advanced NSCLC is an efficient and well-tolerated chemotherapeutic approach.
机译:目的:确定低剂量多西他赛和顺铂(CDDP)联合治疗老年晚期NSCLC患者的疗效和安全性。患者与方法:共有42例年龄≥70岁且先前未接受治疗的晚期NSCLC患者在第1天接受多西他赛75 mg / m(2)加CDDP 50 mg / m(2)。该方案每21天重复一次。除非检测到进行性疾病,否则患者至少接受三个疗程。结果:通过意向性治疗分析,总体缓解率为31%(95%CI,17.8-47.2%)。共有18例患者(43%)病情稳定,进展11例(26%)。进展的中位时间为5.2个月。总体中位生存期为8.9个月,一年精算生存率为41%。东部合作肿瘤小组的表现状态改善了18例(43%)。化疗方案耐受良好。共有11名患者(26%)发生3/4级不良反应:7(17%)中性粒细胞减少(其中一名被诊断为发热性中性粒细胞减少),3(7%)乏力,3(7%)恶心/呕吐, 1(2%)腹泻,1(2%)血小板减少症和1(2%)神经毒性。没有观察到由于毒性导致的死亡。结论:低剂量CDDP联合多西他赛治疗老年晚期非小细胞肺癌是一种有效且耐受性好的化疗方法。

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