首页> 外文期刊>Chemotherapy: International Journal of Experimental and Clinical Chemotherapy >Comparison of the Efficacy between Pemetrexed plus Platinum and Non-Pemetrexed plus Platinum as First-Line Treatment in Patients with Wild-Type Epidermal Growth Factor Receptor Nonsquamous Non-Small Cell Lung Cancer: A Retrospective Analysis
【24h】

Comparison of the Efficacy between Pemetrexed plus Platinum and Non-Pemetrexed plus Platinum as First-Line Treatment in Patients with Wild-Type Epidermal Growth Factor Receptor Nonsquamous Non-Small Cell Lung Cancer: A Retrospective Analysis

机译:培美曲塞加铂与非培美曲塞加铂作为野生型表皮生长因子受体非鳞状非小细胞肺癌患者一线治疗的疗效比较:回顾性分析

获取原文
获取原文并翻译 | 示例
           

摘要

Background: Despite the development of molecular research and targeted therapy, patients with wild-type epidermal growth factor receptor (EGFR) non-small cell lung cancer (NSCLC) still receive platinum doublet chemotherapy as the standard first-line treatment. We investigated the efficacy of first-line regimens in patients with wild-type EGFR nonsquamous NSCLC. Methods: We retrospectively analyzed the efficacy of various platinum doublet regimens as first-line treatments. Between 2007 and 2013, a total of 165 patients with wild-type EGFR nonsquamous NSCLC were included in this study. Results: Seventy-one (43.0%) patients were treated with pemetrexed plus platinum (PP) and 94 (57.0%) with non-pemetrexed plus platinum (NPP). The overall response rate was not different between the PP- and NPP-treated groups (26.8 vs. 28.7%, respectively; p = 0.78). The median progression-free survival (PFS) and overall survival (OS) also showed no differences between the two treatment groups (p = 0.12 for PFS, p = 0.42 for OS). The median PFS and OS for the PP group were 4.6 months (95% CI, 3.8-5.4) and 18.7 months (95% CI, 11.7-25.8), respectively, and for the NPP group, they were 4.2 months (95% CI, 3.4-5.0) and 12.2 months (95% CI, 10.3-14.1), respectively. In the subgroup analysis, most subgroups showed no significant difference in PFS and OS between the two treatment groups. Conclusion: Our data showed that the efficacy of various platinum doublet regimens was similar in patients with wild-type EGFR nonsquamous NSCLC. (C) 2015 S. Karger AG, Basel
机译:背景:尽管分子研究和靶向治疗的发展,野生型表皮生长因子受体(EGFR)非小细胞肺癌(NSCLC)的患者仍接受铂类双线化疗作为标准的一线治疗。我们调查了一线方案在野生型EGFR非鳞状NSCLC患者中的疗效。方法:我们回顾性分析了各种铂双联方案作为一线治疗的疗效。在2007年至2013年之间,该研究共纳入165名野生型EGFR非鳞状非小细胞肺癌患者。结果:71例(43.0%)患者接受培美曲塞加铂(PP)治疗,94例(57.0%)患者接受非培美曲塞加铂(NPP)治疗。 PP和NPP治疗组的总缓解率无差异(分别为26.8和28.7%; p = 0.78)。中位无进展生存期(PFS)和总体生存期(OS)在两个治疗组之间也没有差异(PFS p = 0.12,OS p = 0.42)。 PP组的中位PFS和OS分别为4.6个月(95%CI,3.8-5.4)和18.7个月(95%CI,11.7-25.8),NPP组为4.2个月(95%CI) ,3.4-5.0)和12.2个月(95%CI,10.3-14.1)。在亚组分析中,大多数亚组在两个治疗组之间的PFS和OS没有显着差异。结论:我们的数据表明,在野生型EGFR非鳞状NSCLC患者中,各种铂类双联方案的疗效相似。 (C)2015 S.Karger AG,巴塞尔

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号