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吉非替尼治疗晚期非小细胞肺癌32例的临床观察 被引量:2

Clinical Observation on Gefitinib for the Treatment of Patients with Advanced Non-Small-Cell Lung Cancer
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摘要 目的观察吉非替尼治疗晚期非小细胞肺癌的近期疗效及不良反应。方法32例经放化疗失败的非小细胞肺癌晚期患者,均发生远处转移。口服吉非替尼250mg/次,每天1次,服药中位时间为4个月。结果32例可评价疗效病例中完全缓解0例,部分缓解8例,疾病稳定10例,疾病进展14例,有效率为25.0%(8/32),疾病控制率为56.3%(18/32),中位生存期4.8个月(1~14个月),1年生存率50.0%(16/32)。主要不良反应是皮疹,共有20例(63.5%)。其他不良反应有腹泻、恶心和肝功能损害,无因不良反应退出者。结论吉非替尼治疗晚期非小细胞肺癌有一定疗效,不良反应轻,患者能耐受。 Objective To evaluate the efficacy and toxicities of Gefitinih in patients with advanced non-small cell lung eancer(NSCLC). Methods 32 patients with advanced NSCLC were in stage IV. Gefitinib was administered orally at 250 mg, once a day until cancer progressed or serve toxicities occurred. The median time for administered of Gufitinih was four months. Resuits Among the 32 patients, 8 patients response (PR) , 10 no change (NC) , and 14 progression disease (PD). The total response rate was 25.0% (8/32) and disease control rate was 56.3% (18/32). The median survival time was 4.8 months, The 1-year survival rate was 50.0% (16/32) . The main toxicity of Gefitinib was skin rash . 20 patients had rash,with 63.5% of the whole patients. Conclusion Gifilinib is effective in treatment of advanced NSCLC. The patients had minimum toxicities.
出处 《实用癌症杂志》 2009年第4期384-385,398,共3页 The Practical Journal of Cancer
关键词 非小细胞肺癌 吉非替尼 靶向治疗 表皮生长因子受体 Non-small cell lung cancer(NSCLC) C, efitinih Target therapy Epidermal growth factor reeeptor
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