Predictive markers in elderly patients with estrogen receptor-positive breast cancer treated with aromatase inhibitors: an array-based pharmacogenetic study

被引:12
作者
Rumiato, E. [1 ]
Brunello, A. [2 ]
Ahcene-Djaballah, S. [2 ]
Borgato, L. [3 ]
Gusella, M. [4 ]
Menon, D. [4 ]
Pasini, F. [4 ]
Amadori, A. [1 ,5 ]
Saggioro, D. [1 ]
Zagonel, V. [2 ]
机构
[1] Veneto Inst Oncol IOV IRCCS, Immunol & Mol Oncol Unit, Via Gattamelata 64, I-35128 Padua, Italy
[2] Veneto Inst Oncol IOV IRCCS, Dept Clin & Expt Oncol, Med Oncol Unit 1, Padua, Italy
[3] Med Sci Dept ULSS 13, Hematooncol Unit, Venice, Italy
[4] ULSS 18, Rovigo Gen Hosp, Div Oncol, Rovigo, Italy
[5] Univ Padua, Oncol Sect, Dept Surg Oncol & Gastroenterol, Padua, Italy
关键词
POSTMENOPAUSAL WOMEN; CLINICAL-OUTCOMES; THERAPY; GENE; TAMOXIFEN; LETROZOLE; POLYMORPHISM; EFFICACY; ANASTROZOLE; SUPERIOR;
D O I
10.1038/tpj.2015.73
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
So far, no reliable predictive clinicopathological markers of response to aromatase inhibitors (AIs) have been identified, and little is known regarding the role played by host genetics. To identify constitutive predictive markers, an array- based association study was performed in a cohort of 55 elderly hormone-dependent breast cancer (BC) patients treated with third-generation AIs. The array used in this study interrogates variants in 225 drug metabolism and disposition genes with documented functional significance. Six variants emerged as associated with response to AIs: three located in ABCG1, UGT2A1, SLCO3A1 with a good response, two in SLCO3A1 and one in ABCC4 with a poor response. Variants in the AI target CYP19A1 resulted associated with a favourable response only as haplotype; haplotypes with increased response association were also detected for ABCG1 and SLCO3A1. These results highlight the relevance of host genetics in the response to AIs and represent a first step toward precision medicine for elderly BC patients.
引用
收藏
页码:525 / 529
页数:5
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