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作 者:杨锡贵[1] 贾丽雅[1] 步兵[1] 刘志方[1] 田禾[1] 周登峰[1] 张锡芹[1]
机构地区:[1]山东省肿瘤医院
出 处:《临床肿瘤学杂志》2005年第2期135-136,139,共3页Chinese Clinical Oncology
摘 要:目的:观察和评价吉西他滨(GEM)联合长春瑞滨(NVB)治疗晚期非小细胞肺癌(NSCLC)的疗效和毒性.方法:GEM 1 000 mg/m2加生理盐水(NS)100 ml,30分钟内滴注,第1、8天;NVB 25 mg/m2加NS 70 ml快速静脉推注,第1、8天.21天为1个周期,至少治疗2个周期. 结果:21例NSCLC患者,10例完成2个周期,6例3个周期,5例4个周期,共治疗58个周期.CR 1例,PR 9例,SD 9例,PD 2例,总有效率(CR+PR)为47.6%;初治8例,复治13例,有效率分别为62.5%(5/8例)和38.5%(5/13例)(P<0.05);鳞癌8例,腺癌13例,有效率分别为62.5%(5/8例)和38.5%(5/13例)(P<0.05).中位生存期(MST)11.5个月,1年生存率为42.0%.毒性反应主要有白细胞减少、血小板下降、血红蛋白降低;白细胞减少Ⅲ~Ⅳ度者占28.6%(6/21),血小板下降和血红蛋白下降Ⅲ~Ⅳ度分别为14.3%(3/21)和4.8%(1/21).结论:吉西他滨联合长春瑞滨治疗晚期非小细胞肺癌具有较好的疗效,毒性反应可以耐受,特别是老年患者化疗更适宜.Objective:To evaluate clinical efficacy and toxicity of gemcitabine (GEM) combined with navelbine (NVB) for stage IV non-small cell lung cancer (NSCLC). Methods:Twenty-one cases with stage IV NSCLC were treated with GEM 1 000 mg/m^2 and NVB 25 mg/m^2 every 21 days for at least 2 cycles. Results:The response rate (RR) was 47.6% ( CR = 1, PR =9 ). The therapeutic effect was better in the patients initially diagnozed than in the patients in recurrence ( RR :62.5% VS 38.5% , P 〈 0.05 ). The therapeutic effect in the patients with squamous cell carcinoma was better than in the patients with adenocarcinoma (RR:62.5% VS 38.5% , P 〈 0.05). The major foxicities included leukopenia reciuced and hemoglobin redused. The median survival time was 11.5 months and the 1-year survival rate was 42.0% (95% CI 24% - 59% ). Conclusion:A high response rate was obtained in stage IV NSCLC treated by GEM plus NVB with tolerable toxicity.
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