Table 3
A summary of research studies on neoadjuvant endocrine therapy

Study Design Subject Treatment Clinical response (%) Breast-conserving rate (%)
Eiermann et al., 2001 [44] Randomized 337 Patients Letrozole 55 45
Double-blind Postmenopausal Tamoxifen 36 35
Multicenter ER/PR (+) For 4 mo P<0.001 P=0.022
IMPACT, 2005 [46] Randomized 330 Patients Tamoxifen 36 22
Postmenopausal Anastrozole 37 46
ER (+) Tamoxifen+anastrozole 39 26
Operable For 3 moP=0.03
Locally advanced
PROACT, 2006 [43] Randomzed 451 Patients Tamoxifen 46.2 30.8
Double -blind Postmenopausal Anastrozole 50 43
Multicenter ER/PR (+) For 1 moP=0.04
OperableACOSOG
Locally advanced
Z1031, 2011 [47] Randomized 377 Patients Exemestane 62.9
Phase II Letrozole74.8
Postmenopausal Anastrozole69.1
ER (+) For 16–18 wkFor all patients:
Clinical stage II-IIINo differences in surgical results, PEPI score and Ki-67 suppression
STAGE, 2012 [45] Randomized 197 Patients Goserelin+anastrozole70.4
Double-blind Premenopausal Goserelin+tamoxifen50.5
Phase III ER (+) For 6 moP=0.004
Multicenter HER2 (-)
Operable
ER, estrogen receptor; PR, progesterone receptor; IMPACT, immediate preoperative anastrozole, tamoxifen, or combined with tamoxifen; PROACT, pre-operative "arimidex" compared to tamoxifen; ACOSOG, American college of surgeons oncology group; PEPI, Preoperative endocrine prognostic index.