HER2 expression and efficacy of dose-dense anthracycline-containing adjuvant chemotherapy in breast cancer patients

被引:28
作者
Del Mastro, L
Bruzzi, P
Nicolò, G
Cavazzini, G
Contu, A
D'Amico, M
Lavarello, A
Testore, F
Castagneto, B
Aitini, E
Perdelli, L
Bighin, C
Rosso, R
Venturini, M
机构
[1] Natl Inst Canc Res, Dept Med Oncol, I-16132 Genoa, Italy
[2] Natl Inst Canc Res, Trials Unit, I-16132 Genoa, Italy
[3] Natl Inst Canc Res, Pathol Unit, I-16132 Genoa, Italy
[4] Osped C Poma, Mantua, Italy
[5] UO Oncol Med, Sassari, Italy
[6] Osped Galliera, Genoa, Italy
[7] Osped Civile, Sestri Levante, GE, Italy
[8] Oncol Med, Asti, Italy
关键词
erbB-2; dose density; predictive factors; prognosis;
D O I
10.1038/sj.bjc.6602660
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
No data are available on the role of HER2 overexpression in predicting the efficacy of dose-dense anthracycline-containing adjuvant chemotherapy in breast cancer patients. We retrospectively evaluated this role in patients enrolled in a phase III study comparing standard FEC21 (5-fluorouracil, epirubicin, and cyclophosphamide, administered every 3 weeks) vs dose-dense FEC14 (the same regimen repeated every 2 weeks). HER2 status was determined for 731 of 1214 patients. Statistical analyses were performed to test for interaction between treatment and HER2 status with respect to event-free survival (EFS) and overall survival (OS); EFS and OS were compared within each HER2 subgroup and within each treatment arm. Median follow-up was 6.7 years. Among FEC21-treated patients, both EFS (HR = 2.07; 95% CI 1.27-3.38) and OS (HR = 2.47; 95% CI 1.34-4.57) were significantly worse in HER2+ patients than in HER2- patients. Among FEC14-treated patients, differences in either EFS (HR = 1.21; 95% CI 0.65-2.24) or OS (HR = 1.85; 95% CI 0.88-3.89) between HER2+ and HER2- patients were not statistically significant. Interaction analysis suggested that the use of dose-dense FEC14 might remove the negative prognostic effect of HER2 overexpression on EFS and OS. Our data suggest a potential role of HER-2 overexpression in predicting the efficacy of dose-dense epirubicin-containing chemotherapy and the need to confirm this hypothesis in future prospective studies.
引用
收藏
页码:7 / 14
页数:8
相关论文
共 15 条
[1]  
BORG A, 1991, ONCOGENE, V6, P137
[2]   Randomized trial of dose-dense versus conventionally scheduled and sequential versus concurrent combination chemotherapy as postoperative adjuvant treatment of node-positive primary breast cancer: First report of intergroup trial C9741/cancer and leukemia group B trial 9741 [J].
Citron, ML ;
Berry, DA ;
Cirrincione, C ;
Hudis, C ;
Winer, EP ;
Gradishar, WJ ;
Davidson, NE ;
Martino, S ;
Livingston, R ;
Ingle, JN ;
Perez, EA ;
Carpenter, J ;
Hurd, D ;
Holland, JF ;
Smith, BL ;
Sartor, CI ;
Leung, EH ;
Abrams, J ;
Schilsky, RL ;
Muss, HB ;
Norton, L .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (08) :1431-1439
[3]  
Di Leo A, 2002, CLIN CANCER RES, V8, P1107
[4]   Meeting highlights:: Updated international expert consensus on the primary therapy of early breast cancer [J].
Goldhirsch, A ;
Wood, WC ;
Gelber, RD ;
Coates, AS ;
Thürlimann, B ;
Senn, HJ .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (17) :3357-3365
[5]   HER2 and choice of adjuvant chemotherapy for invasive breast cancer: National Surgical Adjuvant Breast and Bowel Project Protocol B-15 [J].
Paik, S ;
Bryant, J ;
Tan-Chiu, E ;
Yothers, G ;
Park, C ;
Wickerham, DL ;
Wolmark, N .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2000, 92 (24) :1991-1998
[6]   erbB-2 and response to doxorubicin in patients with axillary lymph node-positive, hormone receptor-negative breast cancer [J].
Paik, SM ;
Bryant, J ;
Park, CH ;
Fisher, B ;
Tan-Chiu, E ;
Hyams, D ;
Fisher, ER ;
Lippman, ME ;
Wickerham, DL ;
Wolmark, N .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1998, 90 (18) :1361-1370
[7]   Phase III trial comparing two dose levels of epirubicin combined with cyclophosphamide with cyclophosphamide, methotrexate, and fluorouracil in node-positive breast cancer [J].
Piccart, MJ ;
Di Leo, A ;
Beauduin, M ;
Vindevoghel, A ;
Michel, J ;
Focan, C ;
Tagnon, A ;
Ries, F ;
Gobert, P ;
Finet, C ;
Closon-Dejardin, MT ;
Dufrane, JP ;
Kerger, J ;
Liebens, F ;
Beauvois, S ;
Bartholomeus, S ;
Dolci, S ;
Lobelle, JP ;
Paesmans, M ;
Nogaret, JM .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (12) :3103-3110
[8]  
Ravdin P M, 2001, J Natl Cancer Inst Monogr, P80
[9]  
Schnitt S J, 2001, J Natl Cancer Inst Monogr, P22
[10]  
SLEDGE GW, 2001, J NATL CANC RES I MO, V30, P85