Can predictive biomarkers in breast cancer guide adjuvant endocrine therapy?

被引:63
作者
Beelen, Karin [2 ]
Zwart, Wilbert [2 ]
Linn, Sabine C. [1 ]
机构
[1] Netherlands Canc Inst, Dept Med Oncol, NL-1066 CX Amsterdam, Netherlands
[2] Netherlands Canc Inst, Dept Mol Pathol, NL-1066 CX Amsterdam, Netherlands
关键词
ESTROGEN-RECEPTOR-ALPHA; GROWTH-FACTOR RECEPTOR; TAMOXIFEN RESISTANCE; PIK3CA MUTATIONS; AROMATASE INHIBITORS; PROGESTERONE-RECEPTOR; POSTMENOPAUSAL WOMEN; CYP2D6; GENOTYPE; ER-ALPHA; CYCLIN-E;
D O I
10.1038/nrclinonc.2012.121
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Personalized medicine for oestrogen receptor-alpha (ER alpha)-positive breast cancer requires predictive biomarkers for broad endocrine resistance as well as biomarkers capable of predicting resistance to a specific agent. In addition, biomarkers could be used to select patients that might benefit from the addition of treatments that do not target ERa. However, biomarker identification studies seem to be far from consistent and identified biomarkers seldom face an introduction into clinical practice. Importantly, most of the studies that seek to identify biomarkers have been performed using material from consecutive series of patients treated with tamoxifen (the most commonly prescribed ERa antagonist). Consequently, the predictive value of any biomarker identified is confounded by its prognostic value. Another important issue is the lack of differentiation between premenopausal and postmenopausal patients with breast cancer. The hormonal environment of a tumour in patients who are premenopausal is intrinsically distinct from those arising in postmenopausal women. Biomarkers of different biological mechanisms might enable the prediction of either broad endocrine resistance or resistance to a specific agent in each of these patient subtypes. Ultimately, improvements to study design are needed to establish the clinical validity of the most promising biomarkers to predict benefit from endocrine therapy.
引用
收藏
页码:529 / 541
页数:13
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