Relative Effectiveness of Letrozole Compared With Tamoxifen for Patients With Lobular Carcinoma in the BIG 1-98 Trial

被引:117
作者
Metzger Filho, Otto [1 ]
Giobbie-Hurder, Anita [1 ]
Mallon, Elizabeth
Gusterson, Barry [4 ]
Viale, Giuseppe [5 ]
Winer, Eric P. [1 ]
Thuerlimann, Beat [7 ,8 ]
Gelber, Richard D. [2 ]
Colleoni, Marco [6 ]
Ejlertsen, Bent [9 ]
Debled, Marc [10 ]
Price, Karen N. [3 ]
Regan, Meredith M. [2 ]
Coates, Alan S. [11 ,12 ]
Goldhirsch, Aron [6 ]
机构
[1] Dana Farber Canc Inst, Boston, MA USA
[2] Harvard Univ, Sch Med, Cambridge, MA 02138 USA
[3] Frontier Sci & Technol Res, Boston, MA USA
[4] Univ Glasgow, Inst Canc Sci, Glasgow, Lanark, Scotland
[5] Univ Milan, I-20122 Milan, Italy
[6] European Inst Oncol, Milan, Italy
[7] Kantonsspital, St Gallen, Switzerland
[8] Swiss Grp Clin Canc Res, Bern, Switzerland
[9] Rigshosp, DK-2100 Copenhagen, Denmark
[10] Inst Bergoniie, Bordeaux, France
[11] Int Breast Canc Study Grp, Bern, Switzerland
[12] Univ Sydney, Sydney, NSW 2006, Australia
关键词
EARLY BREAST-CANCER; ADJUVANT ENDOCRINE THERAPY; INTERNATIONAL EXPERT CONSENSUS; POSTMENOPAUSAL WOMEN; NEOADJUVANT CHEMOTHERAPY; PREOPERATIVE CHEMOTHERAPY; AROMATASE INHIBITORS; RANDOMIZED-TRIAL; PREDICTIVE-VALUE; DOUBLE-BLIND;
D O I
10.1200/JCO.2015.60.8133
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To evaluate the relative effectiveness of letrozole compared with tamoxifen for patients with invasive ductal or lobular carcinoma. Patients and Methods Patients diagnosed with early-stage invasive ductal carcinoma (IDC) or classic invasive lobular carcinoma (ILC) who were randomly assigned onto the Breast International Group (BIG) 1-98 trial and who had centrally reviewed pathology data were included (N = 2,923). HER2-negative IDC and ILC were additionally classified as hormone receptor-positive with high (luminal B [LB] -like) or low (luminal A [LA] -like) proliferative activity by Ki-67 labeling index. Survival analyses were performed with weighted Cox models that used inverse probability of censoring weighted modeling. Results The median follow-up time was 8.1 years. In multivariable models for disease-free survival (DFS), significant interactions between treatment and histology (ILC or IDC; P = .006) and treatment and subgroup (LB like or LA like; P = .01) were observed. In the ILC subset, there was a 66% reduction in the hazard of a DFS event with letrozole for LB (hazard ratio [HR], 0.34; 95% CI, 0.21 to 0.55) and a 50% reduction for LA subtypes (HR, 0.50; 95% CI, 0.32 to 0.78). In the IDC subset, there was a significant 35% reduction in the hazard of a DFS event with letrozole for the LB subtype (HR, 0.65; 95% CI, 0.53 to 0.79), but no difference between treatments was noted for IDC and the LA subtype (HR, 0.95; 95% CI, 0.76 to 1.20). Conclusion The magnitude of benefit of adjuvant letrozole is greater for patients diagnosed with lobular carcinoma versus ductal carcinoma. (C) 2015 by American Society of Clinical Oncology
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页码:2772 / U85
页数:14
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