首页> 外文期刊>Annals of oncology: official journal of the European Society for Medical Oncology >Randomised study of sequential versus combination chemotherapy with capecitabine, irinotecan and oxaliplatin in advanced colorectal cancer, an interim safety analysis. A Dutch Colorectal Cancer Group (DCCG) phase III study.
【24h】

Randomised study of sequential versus combination chemotherapy with capecitabine, irinotecan and oxaliplatin in advanced colorectal cancer, an interim safety analysis. A Dutch Colorectal Cancer Group (DCCG) phase III study.

机译:卡培他滨,伊立替康和奥沙利铂序贯或联合化疗在晚期大肠癌中的随机研究,一项临时安全性分析。荷兰大肠癌小组(DCCG)的III期研究。

获取原文
获取原文并翻译 | 示例
           

摘要

BACKGROUND: Results on overall survival in randomised studies of mono- versus combination chemotherapy in advanced colorectal cancer patients may have been biased by an imbalance in salvage treatments. This is the first randomised study that evaluates sequential versus combination chemotherapy with a fluoropyrimidine, irinotecan and oxaliplatin. PATIENTS AND METHODS: A total of 820 patients were randomised between first-line capecitabine, second-line irinotecan and third-line capecitabine + oxaliplatin (arm A) versus first-line capecitabine + irinotecan, and second-line capecitabine + oxaliplatin (arm B). The primary end point was overall survival. We present the results of an interim analysis on the safety data in the first 400 patients. RESULTS: In first-line the incidence of grade 3-4 diarrhoea, nausea, vomiting and febrile neutropenia was significantly higher in arm B. However, when toxicity over all lines was considered only grade 3 hand-foot syndrome occurred more frequently in arm A (12% versus 6%, respectively, P = 0.041). The incidence of cardiovascular toxicity was low. In two out of five patients with sudden death (one in arm A, four in arm B) cardiovascular risk factors were present. CONCLUSIONS: Both treatment arms had an acceptable safety profile. These data imply that the results on survival will be the major determinant for the selection of either strategy. Capecitabine plus irinotecan appears to be a feasible first-line treatment for patients with advanced colorectal carcinoma.
机译:背景:晚期结直肠癌患者单药或联合化疗随机研究的总体生存结果可能因挽救治疗的不平衡而产生偏差。这是第一项随机研究,评估了氟嘧啶,伊立替康和奥沙利铂的序贯化疗与联合化疗。病人和方法:一线卡培他滨,二线伊立替康和三线卡培他滨+奥沙利铂(A组)与一线卡培他滨+伊立替康,二线卡培他滨+奥沙利铂(B组)之间共计820例患者被随机分配)。主要终点是总体生存率。我们提供了对前400名患者的安全性数据进行中期分析的结果。结果:在第一线中,B组的3-4级腹泻,恶心,呕吐和发热性中性粒细胞减少症的发生率显着更高。但是,当考虑到所有系的毒性时,A组仅出现3级手足综合征(分别为12%和6%,P = 0.041)。心血管毒性的发生率低。在五分之二的猝死患者中(A组1例,B组4例)存在心血管危险因素。结论:两个治疗臂的安全性均可接受。这些数据表明,生存结果将是选择这两种策略的主要决定因素。卡培他滨加伊立替康似乎是晚期大肠癌患者可行的一线治疗。

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