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Second-line treatment with irinotecan plus cisplatin vs cisplatin of patients with advanced non-small-cell lung cancer pretreated with taxanes and gemcitabine: a multicenter randomised phase II study

机译:伊立替康联合顺铂与顺铂二线治疗接受紫杉烷类药物和吉西他滨治疗的晚期非小细胞肺癌患者的多中心随机II期研究

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摘要

The aim of this study was to compare the irinotecan/cisplatin regimen with cisplatin as second-line chemotherapy in patients with advanced non-small-cell lung cancer (NSCLC) pretreated with a taxane/gemcitabine regimen. Patients (n=147) with stage IV NSCLC pretreated with a taxane/gemcitabine regimen were randomly assigned to receive either irinotecan (110 mg m−2, day 1 and 100 mg m−2, day 8) and cisplatin (80 mg m−2, day 8) (IC; n=74) or CDDP (80 mg m−2, day 1) (C; n=73) every 3 weeks. Patients treated with IC and C had a median survival of 7.8 and 8.8 months, respectively (P=0.933). The 1-year survival rate was 34.3% for IC-treated patients and 31.7% for C-treated patients. Cox's regression analysis revealed that response to treatment (hazard ratio (HR)=2.787; 95% confidence interval (CI): 1.1578–4.922) and performance status (HR=1.865; 95% CI: 1.199–2.872) was independent prognostic factors for survival. Overall response rate was 22.5% (95% CI: 12.8–32.2%) for IC-treated patients and 7.0% (95% CI: 1.15–13.6%) for C-treated patients (P=0.012); tumour growth control (partial remission (PR)+stable disease (SD)) was observed in 26 (38%) IC and 25 (36%) C patients (P=0.878). There was no difference in terms of quality of life between the two chemotherapy arms. The incidence of febrile neutropenia, grade 3 and 4 neutropenia and grade 3 and 4 diarrhoea was significantly higher in the IC- than the C-treated patients. Other toxicities were mild. There were no treatment-related deaths in either arm. The IC regimen did not confer a survival benefit compared with C as second-line treatment of patients with advanced NSCLC pretreated with a taxane/gemcitabine regimen, despite its better efficacy in terms of response rate.
机译:这项研究的目的是将伊立替康/顺铂方案与顺铂作为接受紫杉烷/吉西他滨方案治疗的晚期非小细胞肺癌(NSCLC)患者的二线化疗方案进行比较。接受紫杉烷/吉西他滨方案预处理的IV期NSCLC患者(n = 147)被随机分配接受伊立替康(110(mg m-2,第1天和100 mg m-2,第8天)和顺铂(80 mg m-2 2,第8天(IC; n = 74)或CDDP(80μmgm-2,第1天)(C; n = 73)每3周一次。接受IC和C治疗的患者的中位生存期分别为7.8和8.8个月(P = 0.933)。接受IC治疗的患者的1年生存率为34.3%,接受C治疗的患者为31.7%。 Cox回归分析显示,对治疗的反应(危险比(HR)= 2.787; 95%置信区间(CI):1.1578–4.922)和表现状态(HR = 1.865; 95%CI:1.199–2.872)是以下因素的独立预后因素:生存。接受IC治疗的患者的总缓解率为22.5%(95%CI:12.8–32.2%),接受C治疗的患者为7.0%(95%CI:1.15–13.6%)(P = 0.012);在26名(38%)IC患者和25名(36%)C患者中观察到肿瘤生长控制(部分缓解(PR)+稳定疾病(SD))(P = 0.878)。两个化疗组之间在生活质量上没有差异。 IC-治疗患者的发热性中性粒细胞减少,3和4级中性粒细胞减少以及3和4级腹泻的发生率显着高于C治疗患者。其他毒性轻微。两组均无与治疗相关的死亡。尽管使用C方案作为紫杉烷/吉西他滨方案预处理的晚期NSCLC患者的二线治疗,但IC方案与C方案相比并没有带来生存优势,尽管它在缓解率方面具有更好的疗效。

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