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

被引:5
作者
Cameron, DA
Anderson, A
Toy, E
Evans, TRJ
Le Vay, JH
Kennedy, ICS
Grieve, RJ
Perren, TJ
Jones, A
Mansi, J
Crown, J
Leonard, RCF
机构
[1] Western Gen Hosp, Dept Oncol, Edinburgh EH4 2XU, Midlothian, Scotland
[2] Velindre Hosp, Dept Oncol, Cardiff, S Glam, Wales
[3] Univ Glasgow, Beatson Oncol Ctr, Dept Med Oncol, Western Infirm, Glasgow, Lanark, Scotland
[4] Suffolk Oncol Ctr, Ipswich, Suffolk, England
[5] Waikato Hosp, Hamilton, New Zealand
[6] Walsgrave Gen Hosp, Dept Radiotherapy, Coventry CV2 2DY, W Midlands, England
[7] St James Univ Hosp, Teaching Hosp NHS Turst, CRUK Clin Ctr Leeds, Leeds LS9 7TF, W Yorkshire, England
[8] Royal Free Hosp, Dept Oncol, London NW3 2QG, England
[9] St George Hosp, Sch Med, London SW17 0RE, England
[10] St Vincents Hosp, Dublin 4, Ireland
[11] Singleton Hosp, Dept Oncol, Swansea SA2 8QA, W Glam, Wales
关键词
anthracycline; adjuvant; breast cancer; survival;
D O I
10.1038/sj.bjc.6600660
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
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. (C) 2002 Cancer Research UK.
引用
收藏
页码:1365 / 1369
页数:5
相关论文
共 11 条
[1]  
Abe O, 1998, LANCET, V352, P930
[2]   Tailored fluorouracil, epirubicin, and cyclophosphamide compared with marrow-supported high-dose chemotherapy as adjuvant treatment for high-risk breast cancer:: a randomised trial [J].
Bergh, J ;
Wiklund, T ;
Erikstein, B ;
Lidbrink, E ;
Lindman, H ;
Malmström, P ;
Kellokumpu-Lehtinen, P ;
Bengtsson, NO ;
Söderlund, G ;
Anker, G ;
Wist, E ;
Ottosson, S ;
Salminen, E ;
Ljungman, P ;
Holte, H ;
Nilsson, J ;
Blomqvist, C ;
Wilking, N .
LANCET, 2000, 356 (9239) :1384-1391
[3]  
BONADONNA G, 1995, JAMA-J AM MED ASSOC, V273, P542
[4]   ADJUVANT CHEMOTHERAPY WITH DOXORUBICIN PLUS CYCLOPHOSPHAMIDE, METHOTREXATE, AND FLUOROURACIL IN THE TREATMENT OF RESECTABLE BREAST-CANCER WITH MORE THAN 3 POSITIVE AXILLARY NODES [J].
BUZZONI, R ;
BONADONNA, G ;
VALAGUSSA, P ;
ZAMBETTI, M .
JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (12) :2134-2140
[5]  
*EARL BREAST CANC, 2000, UNPUB OV DAT POL EAR
[6]  
GOLDIE JH, 1979, CANCER TREAT REP, V63, P1727
[7]  
GOLDIE JH, 1982, CANCER TREAT REP, V66, P439
[8]  
HENDERSON IC, 1998, P AN M AM SOC CLIN, V17, P101
[9]   Randomized trial of intensive cyclophosphamide, epirubicin, and fluorouracil chemotherapy compared with cyclophosphamide, methotrexate, and fluorouracil in premenopausal women with node-positive breast cancer [J].
Levine, MN ;
Bramwell, VH ;
Pritchard, KI ;
Norris, BD ;
Shepherd, LE ;
Abu-Zahra, H ;
Findlay, B ;
Warr, D ;
Bowman, D ;
Myles, J ;
Arnold, A ;
Vandenberg, T ;
MacKenzie, R ;
Robert, J ;
Ottaway, J ;
Burnell, M ;
Williams, CK ;
Tu, DS .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (08) :2651-2658
[10]  
NORTON L, 1992, IMPORTANT ADV ONCOLO, P57