Estrogen-independent proliferation is present in estrogen-receptor HER2-positive primary breast cancer after neoadjuvant letrozole

被引:142
作者
Ellis, Matthew J.
Too, Yu
Young, Oliver
White, Sharon
Proia, Alan D.
Murray, Julliette
Renshaw, Lorna
Faratian, Dana
Thomas, Jeremy
Dowsett, Mitch
Krause, Andreas
Evans, Dean B.
Miller, William R.
Dixon, J. Michael
机构
[1] Washington Univ, Sch Med, Siteman Comprehens Canc Ctr, St Louis, MO 63110 USA
[2] Duke Univ, Med Ctr, Durham, NC 27706 USA
[3] Univ Edinburgh, Edinburgh Breast Unit, Edinburgh EH8 9YL, Midlothian, Scotland
[4] Royal Marsden Hosp, London SW3 6JJ, England
[5] Novartis Pharma AG, Basel, Switzerland
关键词
D O I
10.1200/JCO.2005.04.3034
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To investigate the impact of human epidermal growth factor receptor (HER) 1 and HER2 gene amplification on endocrine therapy responsiveness, a fluorescence in situ hybridization (FISH) study was conducted on tumor samples from 305 postmenopausal patients with stage II and III estrogen receptor (ER)-positive (ER 10%) breast cancers treated on two independent neoadjuvant endocrine therapy trials. Patients and Methods FISH analysis focused on HER1 and/or HER2 immunchistochemistry (IHC)-positive patients and a random selection of HER1/2 IHC-negative patients. HER2 FISH status was correlated with response and changes in the proliferation marker Ki67. Results HER1 was rarely amplified (< 1 %), and HER2 amplification was observed in 9.2% of patients. Letrozole response by clinical measurement (71 % HER2 FISH positive v 71 % HER2 FISH negative), mammogram (44% HER2 FISH positive v 47% HER2 FISH negative), or ultrasound (47% HER2 FISH positive v 54% HER2 FISH negative) was not impaired by HER2 FISH-positive status. In contrast, HER2 FISH-positive tumors showed higher histologic grade (P =.009), higher pretreatment Ki67 (P =.005), and less Ki67 suppression after letrozole when compared with HER2 FISH-negative tumors (P =.0001). Similar observations regarding Ki67 were made in a smaller cohort of tamoxifen-treated tumors. Conclusion Neoadjuvant letrozole is clinically effective in ER-positive HER2 FISH-positive tumors, indicating sensitivity to short-term estrogen deprivation. However, continued proliferation despite ongoing letrozole or tamoxifen treatment in the majority of ER-positive HER2 FISH-positive samples (88%) could imply therapeutic resistance that may manifest later in the clinical course of the disease. Discordance between clinical and biomarker findings in this study serves to emphasize the need for surrogate end point validation in neoadjuvant endocrine trials through correlation with information on long-term outcomes.
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页码:3019 / 3025
页数:7
相关论文
共 20 条
[1]   HER-2/neu and p53 expression versus tamoxifen resistance in estrogen receptor-positive, node-positive breast cancer [J].
Berry, DA ;
Muss, HB ;
Thor, AD ;
Dressler, L ;
Liu, ET ;
Broadwater, G ;
Budman, DR ;
Henderson, IC ;
Barcos, M ;
Hayes, D ;
Norton, L .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (20) :3471-3479
[2]   Role of endocrine therapy in the neoadjuvant surgical setting [J].
Dixon, JM .
ANNALS OF SURGICAL ONCOLOGY, 2004, 11 (01) :18S-23S
[3]   Biomarker changes during neoadjuvant anastrozole, tamoxifen, or the combination: Influence of hormonal status and HER-2 in breast cancer - A study from the IMPACT trialists [J].
Dowsett, M ;
Ebbs, SR ;
Dixon, JM ;
Skene, A ;
Griffith, C ;
Boeddinghaus, I ;
Salter, J ;
Detre, S ;
Hills, M ;
Ashley, S ;
Francis, S ;
Walsh, G ;
Smith, IE .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (11) :2477-2492
[4]  
Dowsett M, 2005, CLIN CANCER RES, V11, p951S
[5]  
Dowsett M, 2001, CANCER RES, V61, P8452
[6]   Preoperative treatment of postmenopausal breast cancer patients with letrozole: A randomized double-blind multicenter study [J].
Eiermann, W ;
Paepke, S ;
Appfelstaedt, J ;
Llombart-Cussac, A ;
Eremin, J ;
Vinholes, J ;
Mauriac, L ;
Ellis, M ;
Lassus, M ;
Chaudri-Ross, HA ;
Dugan, M ;
Borgs, M ;
Semiglazov, V .
ANNALS OF ONCOLOGY, 2001, 12 (11) :1527-1532
[7]  
Ellis MJ, 2003, CANCER RES, V63, P6523
[8]   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
[9]   Aberrant expression of minichromosome maintenance proteins 2 and 5, and Ki-67 in dysplastic squamous oesophageal epithelium and Barrett's mucosa [J].
Going, JJ ;
Keith, WN ;
Neilson, L ;
Stoeber, K ;
Stuart, RC ;
Williams, GH .
GUT, 2002, 50 (03) :373-377
[10]  
Heer K, 2001, CLIN CANCER RES, V7, P3491