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作 者:刘鹏辉[1] 廖国清[1] 王红梅[1] 曲怡梅[1] 解国清[1]
机构地区:[1]解放军总医院第二附属医院肿瘤科,北京市100091
出 处:《中国医院用药评价与分析》2009年第9期700-702,共3页Evaluation and Analysis of Drug-use in Hospitals of China
摘 要:目的:观察吉非替尼和多西他赛+顺铂方案治疗老年晚期非小细胞肺癌(NSCLC)的近期疗效和不良反应。方法:63例65岁以上老年晚期NSCLC患者,单用吉非替尼30例(试验组),250 mg.d-1;对照组33例,行多西他赛+顺铂方案,多西他赛75 mg.(m2)-1,第1天,顺铂75 mg.(m2)-1,第1天。每3周为1个周期,两周期后评价客观疗效及不良反应。结果:两组总有效率试验组33.3%,对照组21.2%,P>0.05;试验组疾病控制率试验组73.3%,对照组51.5%,P<0.01。试验组的毒性反应主要为皮疹和腹泻,对照组的主要毒性为骨髓抑制和胃肠道反应,P<0.05。试验组生活质量高于对照组,P<0.05。结论:单药吉非替尼和多西他赛+顺铂方案均可用于老年晚期非小细胞肺癌的治疗,但吉非替尼疾病控制率高,不良反应轻,耐受性好。OBJECTIVE: To evaluate the efficiency and toxicity of Gefitinib vs.Docetaxel plus Cisplatin for advanced for non-small cell lung cancer(NSCLC)in elderly patients.METHODS: 63 elderly patients with stage Ⅲ or stage Ⅳ NSCLC were enrolled: 30 cases(trial group)were assigned to recieve Oral Gefitinib 250mg daily,the other 33(control group)to receive Doccetaxe [75 mg·(m2)-1] on day 1 plus Cisplatin [DDP,75 mg·(m2)-1] on day 1.Every three weeks(21 days)were defined as one cycle.The efficacy and adverse effects in the two groups were evaluated after two eyeles of treatments.RESULTS: The overall response rate was 33.3% in trial group vs. 21.2% in control group( P 〉 0.05) . The relief rate of elinieal symptoms in trial group was 73.3% vs. 51,5% in control group( P 〈 0.01 ). Tile main toxieities in trial group appeared as skin rash and diarrhea while those in control group appeared as bone marrow depression and the alimentary tract reaction( P 〈 0.05). The score of quality of life in trial group was high than in control group( P〈 0.05). CONCLUSION: Either Gefitinib or Doeetaxel plus Cisplatin can be used for treatment of advanced NSCLC in elderly patients, but Gefitinib treatment showed higher disease control rate, milder toxicity and good tolerabilitvy
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