Relationship between oestrogen receptor status and proliferation in predicting response and long-term outcome to neoadjuvant chemotherapy for breast cancer

被引:110
作者
Jones, Robin L. [1 ]
Salter, Janine [1 ]
A'Hern, Roger [1 ]
Nerurkar, Ash [2 ]
Parton, Marina [2 ]
Reis-Filho, Jorge S. [3 ]
Smith, Ian E. [2 ]
Dowsett, Mitchell [1 ]
机构
[1] Royal Marsden Hosp, Acad Dept Biochem, London SW3 6JJ, England
[2] Royal Marsden Hosp, Breast Unit, London SW3 6JJ, England
[3] Inst Canc Res, Breakthrough Breast Canc Res Ctr, London SW3 6JB, England
关键词
Breast cancer; Neoadjuvant chemotherapy; Proliferation; ER; Pathological complete response; PATHOLOGICAL COMPLETE RESPONSE; PREOPERATIVE CHEMOTHERAPY; BIOLOGICAL MARKERS; PROGNOSTIC-FACTORS; PRIMARY TUMOR; SURVIVAL; EXPRESSION; KI-67; EPIRUBICIN; CARCINOMAS;
D O I
10.1007/s10549-009-0329-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Oestrogen receptor (ER) negative breast cancers are more likely to achieve a pathological complete response (pCR) to neoadjuvant chemotherapy compared to those with ER positive tumours. ER positive tumours exhibit low proliferation and ER negative cancers high proliferation. The aim of this study was to determine to what extent the better response of ER negative cancers correlates with proliferation rate. A retrospective analysis of a prospectively maintained database identified 175 neoadjuvant chemotherapy patients with tissue available for Ki67 analysis. On univariate analysis, pre-therapy Ki67 (P = 0.04), ER status (P = 0.002), HER2 status (P = 0.004) and grade (P = 0.0009) were associated with a pCR. In a multivariate model, HER2 was the only significant predictor of pCR. No significant relationship between pre-therapy Ki67 and relapse-free and overall survival was demonstrated. Ki67 is not an independent predictor of clinical CR or pCR. Aspects of ER status beyond its inverse relationship with proliferation may contribute to its predictive value for pCR.
引用
收藏
页码:315 / 323
页数:9
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