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作 者:王思亮[1] 吴荣[1] 徐兆国[1] 陈晓东[1]
机构地区:[1]中国医科大学盛京医院肿瘤科,沈阳110001
出 处:《中国医师进修杂志》2008年第5期4-6,共3页Chinese Journal of Postgraduates of Medicine
摘 要:目的比较拓扑替康联合卡铂(TC)与足叶乙苷联合卡铂(CE)一线治疗小细胞肺癌的疗效及不良反应。方法初治小细胞肺癌患者69例,TC组(34例):应用拓扑替康1mg/m2,静脉滴注,第1—5天,卡铂300mg/m2,静脉滴注,第1天。CE组(35例):应用足叶乙苷100mg/d,静脉滴注,第1—5天,卡铂300mg/m2,静脉滴注,第1天。两种方案均以21d为1个周期。2个周期后评价疗效及不良反应。结果TC组有效率为76.5%,CE组有效率为71.4%,两组比较差异无统计学意义,P〉0.05;TC组无进展生存期为4.1个月,CE组无进展生存期为2.6个月,两组比较差异有统计学意义,P〈0.05;两组不良反应发生率比较差异均无统计学意义,P〉0.05。结论与足叶乙苷联合卡铂方案相比,拓扑替康联合卡铂方案疗效相似,不良反应相近,且无进展生存期延长,是小细胞肺癌一线治疗的安全有效方案。Objective To assess the efficacy and toxicity of topotecan hydrochloride plus carboplatin (TC)versus etoposide plus carboplatin (CE)in patients for previously untreated small cell lung cancer (SCLC). Methods Sixty-nine patients with previously untreated SCLC, TC group (34 cases)were treated with topotecan 1 mg/m2 from day 1 to day 5 and carboplatin 300 mg/ m2 on day 1. CE group (35 cases) were treated with etoposide 100 mg/d from day 1 to day 5 and carboplatin 300mg/m2 on day 1. Treatment was repeated every 3 weeks. The efficacy and toxicity were evaluated in patients who received two cycles of chemotherapy. Results The total effective rate was 76.5% in TC group and 71.4% in CE group (P 〉 0.05 ). The progression-free survival interval was 4.1 months in TC group and :2.6 months in CE group (P 〈 0.05 ). There was no significant difference in the most common toxicities between two groups(P 〉 0.05 ). Conclusion Compared with etoposide plus carboplatin, topotecan plus carboplatin has similar total effective rate, and indifferent toxicities, and the longer progression-flee survival interval, so it is a safe and effective first -line treatment for SCLC.
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