Cyclophosphamide, Epirubicin, and Fluorouracil Versus Dose-Dense Epirubicin and Cyclophosphamide Followed by Paclitaxel Versus Doxorubicin and Cyclophosphamide Followed by Paclitaxel in Node-Positive or High-Risk Node-Negative Breast Cancer

被引:125
作者
Burnell, Margot
Levine, Mark N.
Chapman, Judith-Anne W.
Bramwell, Vivien
Gelmon, Karen
Walley, Barbara
Vandenberg, Ted
Chalchal, Haji
Albain, Kathy S.
Perez, Edith A.
Rugo, Hope
Pritchard, Kathleen
O'Brien, Patti
Shepherd, Lois E.
机构
[1] Atlantic Hlth Sci Corp, St John, NB, Canada
[2] McMaster Univ, Hamilton, ON, Canada
[3] Queens Univ, Natl Canc Inst Canada, Clin Trials Grp, Kingston, ON, Canada
[4] Sunnybrook Odette Canc Ctr, Toronto, ON, Canada
[5] London Reg Canc Ctr, London, ON N6A 4L6, Canada
[6] Tom Baker Canc Clin, Calgary, AB, Canada
[7] British Columbia Canc Agcy, Vancouver Canc Ctr, Vancouver, BC V5Z 4E6, Canada
[8] Allan Blair Canc Ctr, Regina, SK, Canada
[9] SW Oncol Grp, Maywood, IL USA
[10] N Cent Canc Treatment Grp, Jacksonville, FL USA
[11] Canc & Leukemia Grp B, San Francisco, CA USA
基金
美国国家卫生研究院;
关键词
SURGICAL ADJUVANT BREAST; CLINICAL-TRIALS; RANDOMIZED-TRIAL; CHEMOTHERAPY; METHOTREXATE; INSTRUMENT; QUALITY; REGIMEN; LIFE; HER2;
D O I
10.1200/JCO.2009.22.1077
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose Cyclophosphamide, epirubicin, and fluorouracil (CEF) and doxorubicin and cyclophosphamide (AC) followed by paclitaxel (T) are commonly used adjuvant regimens in women with early breast cancer. In a previous trial in women with locally advanced breast cancer, 3 months of high-dose epirubicin and cyclophosphamide (EC) administered every 2 weeks (dose-dense) was equivalent to 6 months of CEF. We hypothesized that 3 months of paclitaxel after dose-dense EC (EC/T) would be superior to CEF or AC/T. Methods After lumpectomy or mastectomy, women 60 years of age or younger with axillary node-positive or high-risk node-negative breast cancer were randomly assigned to receive CEF, EC/T, or AC/T for 6 months. This article reports the interim analysis for recurrence-free survival (RFS), which was planned after 227 recurrences. Results A total of 2,104 patients were enrolled. The median follow-up is 30.4 months. Hazard ratios for recurrence are as follows: AC/T versus CEF, 1.49 (95% CI, 1.12 to 1.99), P = .005; AC/T versus EC/T, 1.68 (95% CI, 1.25 to 2.27), P = .0006; and EC/T versus CEF, 0.89 (95% CI, 0.64 to 1.22), P = .46. Three-year RFS rates for CEF, EC/T, and AC/T are 90.1%, 89.5%, and 85.0%, respectively. There was more febrile neutropenia with CEF (22.3%) and EC/T (16.4%) compared with AC/T (4.8%), but more neuropathy with the last two regimens. Conclusion Three-weekly AC/T is significantly inferior to CEF or EC/T in terms of RFS. It is too early to detect any difference between CEF and dose-dense EC/T.
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页码:77 / 82
页数:6
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