首页> 外文期刊>Annals of oncology: official journal of the European Society for Medical Oncology >Randomized phase III study of cisplatin plus irinotecan versus carboplatin plus paclitaxel, cisplatin plus gemcitabine, and cisplatin plus vinorelbine for advanced non-small-cell lung cancer: Four-Arm Cooperative Study in Japan.
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Randomized phase III study of cisplatin plus irinotecan versus carboplatin plus paclitaxel, cisplatin plus gemcitabine, and cisplatin plus vinorelbine for advanced non-small-cell lung cancer: Four-Arm Cooperative Study in Japan.

机译:顺铂加伊立替康与卡铂加紫杉醇,顺铂加吉西他滨,顺铂加长春瑞滨对晚期非小细胞肺癌的随机III期研究:日本的四臂合作研究。

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BACKGROUND: To compare the efficacy and toxicity of three platinum-based combination regimens against cisplatin plus irinotecan (IP) in patients with untreated advanced non-small-cell lung cancer (NSCLC) by a non-inferiority design. PATIENTS AND METHODS: A total of 602 patients were randomly assigned to one of four regimens: cisplatin 80 mg/m(2) on day 1 plus irinotecan 60 mg/m(2) on days 1, 8, 15 every 4 weeks (IP) carboplatin AUC 6.0 min x mg/mL (area under the concentration-time curve) on day 1 plus paclitaxel 200 mg/m(2) on day 1 every 3 weeks (TC); cisplatin 80 mg/m(2) on day 1 plus gemcitabine 1000 mg/m(2) on days 1, 8 every 3 weeks (GP); and cisplatin 80 mg/m(2) on day 1 plus vinorelbine 25 mg/m(2) on days 1, 8 every 3 weeks (NP). RESULTS: The response rate, median survival time, and 1-year survival rate were 31.0%, 13.9 months, 59.2%, respectively, in IP; 32.4%, 12.3 months, 51.0% in TC; 30.1%, 14.0 months, 59.6% in GP; and 33.1%, 11.4 months, 48.3% in NP. No statistically significant differences were found in response rate or overall survival, but the non-inferiority of none of the experimental regimens could be confirmed. All the four regimens were well tolerated. CONCLUSION: The four regimens have similar efficacy and different toxicity profiles, and they can be used to treat advanced NSCLC patients.
机译:背景:通过非劣效性设计,比较三种铂类联合方案对顺铂加伊立替康(IP)的治疗方案,对未经治疗的晚期非小细胞肺癌(NSCLC)患者的疗效和毒性。患者与方法:共有602名患者被随机分配为以下四种方案之一:第1天的顺铂80 mg / m(2)加每4周第1、8、15天的伊立替康60 mg / m(2)(IP )每3周(TC)在第1天加用卡铂AUC 6.0 min x mg / mL(浓度-时间曲线下的面积)加上在第1天紫杉醇200 mg / m(2);第1天每天80毫克/平方米(2)顺铂,第1天,第8天每3周增加吉西他滨1000毫克/平方米(2)(GP);第1天每天服用顺铂80 mg / m(2),第1天每天服用长春瑞滨25 mg / m(2),每3周一次(NP)。结果:IP患者的缓解率,中位生存时间和1年生存率分别为31.0%,13.9个月和59.2%。 TC中32.4%,12.3个月,51.0%; GP的30.1%,14.0个月,59.6%; NP占33.1%,11.4个月,48.3%。在反应率或总生存率上没有发现统计学上的显着差异,但是没有一个实验方案的非劣效性可以得到证实。四种方案均耐受良好。结论:这四种方案具有相似的疗效和不同的毒性,可用于治疗晚期非小细胞肺癌。

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