Favorable outcome in patients with breast cancer in the presence of pathological response after neoadjuvant endocrine therapy

被引:25
作者
Akashi-Tanaka, Sadako [1 ]
Omatsu, Mutsuko [2 ,4 ]
Shimizu, Chikako [3 ]
Ando, Masashi [3 ]
Terada, Kotoe [1 ]
Shien, Tadahiko [1 ]
Kinoshita, Takayuki [1 ]
Fujiwara, Yasuhiro [3 ]
Seki, Kunihiko [2 ]
Hasegawa, Tadashi [2 ,4 ]
Fukutomi, Takashi [1 ,5 ]
机构
[1] Natl Canc Ctr, Div Breast Surg, Chuo Ku, Tokyo 1040045, Japan
[2] Natl Canc Ctr, Res Inst, Div Pathol, Tokyo 104, Japan
[3] Natl Canc Ctr, Div Med Oncol, Tokyo 1040045, Japan
[4] Sapporo Med Univ, Sch Med, Dept Surg Pathol, Sapporo, Hokkaido, Japan
[5] Aichi Med Univ, Dept Breast & Endocrine Surg, Aichi, Japan
关键词
breast cancer; Ki-67; neoadjuvant endocrine therapy; pathological response; prognostic factor;
D O I
10.1016/j.breast.2007.02.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Neoadjuvant endocrine therapy (NAET) can expand the number of breast cancer patients who can be treated with breast-conserving surgery and can predict benefit from adjuvant endocrine therapy. Because no validated surrogate markers for long-term outcome have been established, we conducted prospective trials to evaluate pathological response and Ki-67 index following treatment with tamoxifen or anastrozole. The study population included postmenopausal women with operable breast tumors that were both estrogen and progesterone receptor-positive and larger than 3 cm. Response was classified as pathological response (minimal response or better) and non-response. Non-responding (25.5%, vs. response 85.9%, p = 0.002), axillary node-positive (58.4% vs. node negative 100%, p=0.045), and high pretreatment Ki-67 index (41.4% vs. low Ki-67 87.1%, p=0.03) patients were significantly associated with poor 5-year relapse-free survival. Multivariate analysis of relapse-free survival indicated that pathological response was independent. Therefore, pathological response may be a favorable prognostic factor after NAET. (c) 2007 Elsevier Ltd. Alt rights reserved.
引用
收藏
页码:482 / 488
页数:7
相关论文
共 17 条
[1]
Comparison of anastrozole versus tamoxifen as preoperative therapy in postmenopausal women with hormone receptor-positive breast cancer - The Pre-Operative "Arimidex" Compared to Tamoxilen (PROAC7) trial [J].
Cataliotti, L ;
Buzdar, AU ;
Noguchi, S ;
Bines, J ;
Takatsuka, Y ;
Petrakova, K ;
Dube, P ;
de Oliveira, CT .
CANCER, 2006, 106 (10) :2095-2103
[2]
Biologic markers as predictors of clinical outcome from systemic therapy for primary operable breast cancer [J].
Chang, J ;
Powles, TJ ;
Allred, DC ;
Ashey, SE ;
Clark, GM ;
Makris, A ;
Assersohn, L ;
Gregory, RK ;
Osborne, CK ;
Dowsett, M .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (10) :3058-3063
[3]
Role of endocrine therapy in the neoadjuvant surgical setting [J].
Dixon, JM .
ANNALS OF SURGICAL ONCOLOGY, 2004, 11 (01) :18S-23S
[4]
Dowsett M, 2005, CLIN CANCER RES, V11, p951S
[5]
Neoadjuvant endocrine therapy for breast cancer: More questions than answers [J].
Ellis, MJ .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (22) :4842-4844
[6]
Letrozole is more effective neoadjuvant endocrine therapy than tamoxifen for ErbB-1- and/or ErbB-2-positive, estrogen receptor-positive primary breast cancer:: Evidence from a phase III randomized trial [J].
Ellis, MJ ;
Coop, A ;
Singh, B ;
Mauriac, L ;
Llombert-Cussac, A ;
Jänicke, F ;
Miller, WR ;
Evans, DB ;
Dugan, M ;
Brady, C ;
Quebe-Fehling, E ;
Borgs, M .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (18) :3808-3816
[7]
Effect of preoperative chemotherapy on the outcome of women with operable breast cancer [J].
Fisher, B ;
Bryant, J ;
Wolmark, N ;
Mamounas, E ;
Brown, A ;
Fisher, ER ;
Wickerham, DL ;
Begovic, M ;
DeCillis, A ;
Robidoux, A ;
Margolese, RG ;
Cruz, AB ;
Hoehn, JL ;
Lees, AW ;
Dimitrov, NV ;
Bear, HD .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (08) :2672-2685
[8]
Johnston SRD, 1999, CANCER RES, V59, P3646
[9]
Preoperative (neoadjuvant) systemic treatment of breast cancer [J].
Kaufmann, M ;
von Minckwitz, G ;
Rody, A .
BREAST, 2005, 14 (06) :576-581
[10]
A multigene assay to predict recurrence of tamoxifen-treated, node-negative breast cancer [J].
Paik, S ;
Shak, S ;
Tang, G ;
Kim, C ;
Baker, J ;
Cronin, M ;
Baehner, FL ;
Walker, MG ;
Watson, D ;
Park, T ;
Hiller, W ;
Fisher, ER ;
Wickerham, DL ;
Bryant, J ;
Wolmark, N .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (27) :2817-2826