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顺铂联合伊立替康对比卡铂联合紫杉醇、顺铂联合吉西他滨以及顺铂联合长春瑞滨治疗晚期非小细胞肺癌的随机III期研究:日本四臂协作研究

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.

作者信息

Ohe Y, Ohashi Y, Kubota K, Tamura T, Nakagawa K, Negoro S, Nishiwaki Y, Saijo N, Ariyoshi Y, Fukuoka M

机构信息

Department of Internal Medicine, National Cancer Center Hospital, Tokyo, Japan.

出版信息

Ann Oncol. 2007 Feb;18(2):317-23. doi: 10.1093/annonc/mdl377. Epub 2006 Nov 1.

Abstract

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.

摘要

背景

采用非劣效性设计比较三种铂类联合方案与顺铂加伊立替康(IP)方案治疗初治晚期非小细胞肺癌(NSCLC)患者的疗效和毒性。

患者与方法

总共602例患者被随机分配至以下四种方案之一:第1天给予顺铂80mg/m²,每4周的第1、8、15天给予伊立替康60mg/m²(IP);第1天给予卡铂AUC 6.0min·mg/mL(浓度-时间曲线下面积),每3周的第1天给予紫杉醇200mg/m²(TC);第1天给予顺铂80mg/m²,每3周的第1、8天给予吉西他滨1000mg/m²(GP);第1天给予顺铂80mg/m²,每3周的第1、8天给予长春瑞滨25mg/m²(NP)。

结果

IP方案的缓解率、中位生存时间和1年生存率分别为31.0%、13.9个月、59.2%;TC方案分别为32.4%、12.3个月、51.0%;GP方案分别为30.1%、14.0个月、59.6%;NP方案分别为33.1%、11.4个月、48.3%。缓解率或总生存方面未发现统计学显著差异,但无法证实任何一种试验方案的非劣效性。所有四种方案耐受性良好。

结论

四种方案疗效相似但毒性特征不同,均可用于治疗晚期NSCLC患者。

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