Prognostic significance of Ki-67 labeling index after short-term presurgical tamoxifen in women with ER-positive breast cancer

被引:70
|
作者
DeCensi, A. [1 ,2 ]
Guerrieri-Gonzaga, A. [2 ]
Gandini, S. [3 ]
Serrano, D. [2 ]
Cazzaniga, M. [2 ]
Mora, S. [2 ]
Johansson, H. [2 ]
Lien, E. A. [4 ,5 ]
Pruneri, G. [6 ,7 ]
Viale, G. [6 ,7 ]
Bonanni, B. [2 ]
机构
[1] EO Osped Galliera, Div Med Oncol, Med Oncol Unit, I-16128 Genoa, Italy
[2] European Inst Oncol, Div Canc Prevent & Genet, Milan, Italy
[3] European Inst Oncol, Div Epidemiol & Biostat, Milan, Italy
[4] Haukeland Hosp, Hormone Lab, N-5021 Bergen, Norway
[5] Univ Bergen, Inst Med, Endocrinol Sect, Bergen, Norway
[6] European Inst Oncol, Div Pathol, Milan, Italy
[7] Univ Milan, Sch Med, Milan, Italy
关键词
breast cancer; Ki-67; predictive biomarker; prognostic biomarker; tamoxifen; LOW-DOSE TAMOXIFEN; RANDOMIZED-TRIAL; POSTMENOPAUSAL WOMEN; ENDOCRINE THERAPY; PREDICTIVE-VALUE; EXPRESSION; RECURRENCE; LETROZOLE; ESTROGEN; SURVIVAL;
D O I
10.1093/annonc/mdq427
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Studies have shown that Ki-67 response after short-term neoadjuvant aromatase inhibitors may predict recurrence in postmenopausal breast cancer, whereas its prognostic effect in premenopausal women is unknown. Patients and methods: We compared the prognostic and predictive value of baseline and post-treatment Ki-67 in 120 pre- and postmenopausal women with early-stage estrogen receptor-positive breast cancer who participated in a 4-week presurgical trial of tamoxifen. Results: After 7.2 years of follow-up, women with post-treatment Ki-67 in the second (14%-19%), third (20%-29%) and top (>= 30%) quartiles had a recurrence hazard ratio of 2.92 [95% confidence interval (CI) 0.95-8.96], 4.37 (1.56-12.25) and 6.05 (2.07-17.65), respectively, as compared with those in the bottom quartile (<14%) (P-trend = 0.001). The risk of invasive disease recurrence was 2.2% (95% CI 0.9-5.0) per point increase in baseline Ki-67 (P-trend = 0.076) and 5.0% (95% CI 2.3-7.7) per point increase in post-tamoxifen Ki-67 (P-trend < 0.001). The risk of death was 5.5 (95% CI 1.26-23.16) times higher in patients with post-drug Ki-67 >= 20% than in those with Ki-67 <20% (P-trend = 0.006). Conclusions: Ki-67 response after short-term neoadjuvant tamoxifen is a good predictor of recurrence-free survival and overall survival, further supporting its use as surrogate biomarker to personalize adjuvant treatment and to screen novel drugs cost-effectively.
引用
收藏
页码:582 / 587
页数:6
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