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间歇序贯阿霉素CMF方案——高危辅助性乳腺癌的最佳非清髓性化疗方案?

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

作者信息

Cameron D A, Anderson A, Toy E, Evans T R J, Le Vay J H, Kennedy I C S, Grieve R J, Perren T J, Jones A, Mansi J, Crown J, Leonard R C F

机构信息

Department of Oncology, Western General Hospital, Crewe Road South, Edinburgh EH4 2XU, Scotland, UK.

出版信息

Br J Cancer. 2002 Dec 2;87(12):1365-9. doi: 10.1038/sj.bjc.6600660.

Abstract

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.

摘要

在米兰公布了关于辅助使用由四个周期阿霉素随后八个周期静脉注射CMF组成的序贯疗法的10年生存数据后,许多中心将其作为高危、多淋巴结阳性乳腺癌的标准治疗方案。因此,它被确定为盎格鲁-凯尔特人辅助大剂量化疗试验的标准组。本研究报告了该方案在329例至少累及四个腋窝淋巴结的早期乳腺癌女性中的应用经验,这些患者未参加任何辅助化疗试验。中位随访3年时,总体5年无病生存率为61%,总生存率为70%。这些数据证实了该方案在非试验患者中的疗效,并且对于相同的高危亚组,表明这种方法提供的结果至少与CALGB 9344 AC-紫杉醇组以及NCIC第1天和第8天CEF方案所见结果一样好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e11/2376297/720c254306e5/87-6600660f1.jpg

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