首页> 外文OA文献 >“A randomised factorial trial of sequential doxorubicin and CMF vs CMF and chemotherapy alone vs chemotherapy followed by goserelin plus tamoxifen as adjuvant treatment of node-positive breast cancer”
【2h】

“A randomised factorial trial of sequential doxorubicin and CMF vs CMF and chemotherapy alone vs chemotherapy followed by goserelin plus tamoxifen as adjuvant treatment of node-positive breast cancer”

机译:“序贯性阿霉素和CMF对比CMF单独化疗与化学疗法联合化疗之后再用戈舍瑞林加他莫昔芬作为淋巴结阳性乳腺癌的辅助治疗的随机因素试验”

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The sequential doxorubicin → CMF (CMF = cyclophosphamide, methotrexate, fluorouracil) regimen has never been compared to CMF in a randomised trial. The role of adding goserelin and tamoxifen after chemotherapy is unclear. In all, 466 premenopausal node-positive patients were randomised to: (a) CMF × 6 cycles (CMF); (b) doxorubicin × 4 cycles followed by CMF × 6 cycles (A → CMF); (c) CMF × 6 cycles followed by goserelin plus tamoxifen × 2 years (CMF → GT); and (d) doxorubicin × 4 cycles followed by CMF × 6 cycles followed by goserelin plus tamoxifen × 2 years (A → CMF → GT). The study used a 2 × 2 factorial experimental design to assess: (1) the effect of the chemotherapy regimens (CMF vs A × CMF or arms a + c vs b + d) and (2) the effect of adding GT after chemotherapy (arms a + b vs c + d). At a median follow-up of 72 months, A → CMF as compared to CMF significantly improved disease-free survival (DFS) with a multivariate hazard ratio (HR) = 0.740 (95% confidence interval (CI): 0.556-0.986; P = 0.040) and produced a nonsignificant improvement of overall survival (OS) (HR = 0.764; 95% CI: 0.489-1.193). The addition of GT after chemotherapy significantly improved DFS (HR = 0.74; 95% CI: 0.555-0.987; P = 0.040), with a nonsignificant improvement of OS (HR = 0.84; 95% CI: 0.54-1.32). A → CMF is superior to CMF. Adding GT after chemotherapy is beneficial for premenopausal node-positive patients. © 2005 Cancer Research UK.
机译:顺序性阿霉素→CMF(CMF =环磷酰胺,甲氨蝶呤,氟尿嘧啶)方案从未在随机试验中与CMF进行比较。化疗后添加戈舍瑞林和他莫昔芬的作用尚不清楚。总共466名绝经前淋巴结阳性患者被随机分为:(a)CMF×6周期(CMF); (b)阿霉素×4周期,然后是CMF×6周期(A→CMF); (c)CMF×6个周期,之后是戈舍瑞林加他莫昔芬×2年(CMF→GT); (d)阿霉素×4个周期,然后是CMF×6个周期,然后是戈舍瑞林加他莫昔芬×2年(A→CMF→GT)。该研究使用2×2阶乘实验设计评估:(1)化疗方案的效果(CMF vs A×CMF或arm a + c vs b + d)和(2)化疗后添加GT的效果(手臂a + b vs c + d)。在72个月的中位随访中,与CMF相比,A→CMF显着改善了无病生存期(DFS),多元风险比(HR)= 0.740(95%置信区间(CI):0.556-0.986; P = 0.040)并没有显着改善总体生存率(HR)(HR = 0.764; 95%CI:0.489-1.193)。化疗后添加GT可以显着改善DFS(HR = 0.74; 95%CI:0.555-0.987; P = 0.040),而OS的改善无统计学意义(HR = 0.84; 95%CI:0.54-1.32)。 A→CMF优于CMF。化疗后添加GT对绝经前结节阳性患者有利。 ©2005英国癌症研究。

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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