Sequential preoperative or postoperative docetaxel added to preoperative doxorubicin plus cyclophosphamide for operable breast cancer: National Surgical Adjuvant Breast and Bowel Project Protocol B-27

被引:735
作者
Bear, HD
Anderson, S
Smith, RE
Geyer, CE
Mamounas, EP
Fisher, B
Brown, AM
Robidoux, A
Margolese, R
Kahlenberg, MS
Paik, S
Soran, A
Wickerham, DL
Wolmark, N
机构
[1] Natl Surg Adjuvant Breast & Bowel Project, Pittsburgh, PA USA
[2] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Biostat, Pittsburgh, PA 15261 USA
[3] Univ Pittsburgh, Dept Surg, Pittsburgh, PA USA
[4] Allegheny Gen Hosp, Pittsburgh, PA 15212 USA
[5] Reg Canc Ctr, Erie, PA USA
[6] Virginia Commonwealth Univ, Med Coll Virginia, Sch Med, Richmond, VA 23298 USA
[7] Virginia Commonwealth Univ, Med Coll Virginia, Massey Canc Ctr, Richmond, VA 23298 USA
[8] Aultman Hosp Canc Ctr, Canton, OH USA
[9] Univ Texas, Hlth Sci Ctr, San Antonio, TX USA
[10] Montreal Gen Hosp, Hotel Dieu, Montreal, PQ, Canada
[11] McGill Univ, Jewish Gen Hosp, Montreal, PQ H3T 1E2, Canada
关键词
D O I
10.1200/JCO.2005.04.1665
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose This study was designed to determine the effect of adding docetaxel (T) to preoperative doxorubicin and cyclophosphamide (AC) on breast cancer response rates and disease-free survival (DFS) and overall survival (OS). Patients and Methods Women with operable breast cancer (N=2,411) were randomly assigned to receive preoperative AC followed by surgery, AC followed by T and surgery, or AC followed by surgery and then T. Tamoxifen was initiated concurrently with chemotherapy. Median time on study for 2,404 patients with follow-up was 77.9 months. Results Addition of T to AC did not significantly impact DFS or OS. There were trends toward improved DFS with addition of T. The addition of T reduced the incidence of local recurrences as first events (P=.0034). Preoperative T, but not postoperative T, significantly improved DFS in patients who had a clinical partial response after AC (hazard ratio [HR]=0.71; 95% CI, 0.55 to 0.91; P=.007). Pathologic complete response, which was doubled by addition of preoperative T, was a significant predictor of OS regardless of treatment (HR=0.33; 95% CI, 0.23 to 0.47; P<.0001). Pathologic nodal status after chemotherapy was a significant predictor of OS (P<.0001). Conclusion The addition of preoperative or postoperative T after preoperative AC did not significantly affect OS, slightly improved DFS, and decreased the incidence of local recurrences, The sample size of this study was not sufficient to yield significance for the moderate DFS improvement. Concurrent use of tamoxifen may have limited the impact of adding T.
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页码:2019 / 2027
页数:9
相关论文
共 73 条
[1]   PACLITAXEL ACTIVITY IN HEAVILY PRETREATED BREAST-CANCER - A NATIONAL-CANCER-INSTITUTE TREATMENT REFERRAL CENTER TRIAL [J].
ABRAMS, JS ;
VENA, DA ;
BALTZ, J ;
ADAMS, J ;
MONTELLO, M ;
CHRISTIAN, M ;
ONETTO, N ;
DESMONDHELLMANN, S ;
CANETTA, R ;
FRIEDMAN, MA ;
ARBUCK, SG .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (08) :2056-2065
[2]  
[Anonymous], J R STAT SOC
[3]  
[Anonymous], [No title captured]
[4]   Gene expression profiles predict complete pathologic response to neoadjuvant paclitaxel and fluorouracil, doxorubicin, and cyclophosphamide chemotherapy in breast cancer [J].
Ayers, M ;
Symmans, WF ;
Stec, J ;
Damokosh, AI ;
Clark, E ;
Hess, K ;
Lecocke, M ;
Metivier, J ;
Booser, D ;
Ibrahim, N ;
Valero, V ;
Royce, M ;
Arun, B ;
Whitman, G ;
Ross, J ;
Sneige, N ;
Hortobagyi, GN ;
Pusztai, L .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (12) :2284-2293
[5]   The effect on tumor response of adding sequential preoperative docetaxel to preoperative doxorubicin and cyclophosphamide: Preliminary results from national surgical adjuvant breast and bowel project protocol B-27 [J].
Bear, HD ;
Anderson, S ;
Brown, A ;
Smith, R ;
Mamounas, EP ;
Fisher, B ;
Margolese, R ;
Theoret, H ;
Soran, A ;
Wickerham, DL ;
Wolmark, N .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (22) :4165-4174
[6]  
Bear HD, 1998, SEMIN ONCOL, V25, P3
[7]  
Berry DA, 2004, BREAST CANCER RES TR, V88, pS17
[8]   Primary chemotherapy in operable breast cancer: Eight-year experience at the Milan Cancer Institute [J].
Bonadonna, G ;
Valagussa, P ;
Brambilla, C ;
Ferrari, L ;
Moliterni, A ;
Terenziani, M ;
Zambetti, M .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (01) :93-100
[9]  
Buchholz TA, 2001, CANCER J, V7, P413
[10]  
CALAIS G, 1994, CANCER, V74, P1283, DOI 10.1002/1097-0142(19940815)74:4<1283::AID-CNCR2820740417>3.0.CO