首页> 外文OA文献 >Block sequential adriamycin CMF – optimal non-myeloablative chemotherapy for high risk adjuvant breast cancer?
【2h】

Block sequential adriamycin CMF – optimal non-myeloablative chemotherapy for high risk adjuvant breast cancer?

机译:阻断序贯阿霉素CmF - 最佳非清髓性化疗治疗高危辅助乳腺癌?

摘要

After the publication of the 10-year survival data from Milan on the adjuvant use of the block sequential regimen consisting of four cycles of adriamycin followed by eight cycles of intravenous CMF, many centres adopted this as standard of care for high risk, multiple node-positive breast cancer. For this reason it was identified as the standard arm for the Anglo-Celtic adjuvant high-dose chemotherapy trial. This study reports on the experience of this regimen in 329 women with early breast cancer involving at least four axillary nodes, who were treated outside any adjuvant chemotherapy trial. At a median follow-up of 3 years, the overall 5-year disease-free survival is 61%, and the overall survival is 70%. These data confirm the efficacy of this regimen in non-trial patients, and, for the same high risk subgroup, indicate that this approach offers an outcome at least as good as that seen in the CALGB 9344 AC-Taxol arm, and the NCIC days 1 and 8 CEF.
机译:米兰发布10年生存率数据后,关于辅助治疗包括4个周期的阿霉素和8个周期的静脉CMF的逐次序贯疗法的辅助使用,许多中心将其作为高危,多结阳性乳腺癌。因此,它被确定为盎格鲁-凯尔特人辅助高剂量化疗试验的标准组。这项研究报告了该方案在329例早期乳腺癌中涉及至少四个腋窝淋巴结的妇女的经验,这些妇女在任何辅助化疗试验之外均得到治疗。在3年的中位随访中,总体5年无病生存率为61%,总体生存率为70%。这些数据证实了该方案在非试验患者中的疗效,并且对于相同的高风险亚组,表明该方法所提供的结果至少与CALGB 9344 AC-Taxol组和NCIC天数相同1和8 CEF。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利

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