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乳腺癌治疗的药物遗传学。

Pharmacogenetics of breast cancer therapies.

机构信息

UNC Institute for Pharmacogenomics and Individualized Therapy, Division of Pharmacotherapy and Experimental Therapeutics, University of North Carolina, Chapel Hill, NC 27599, USA.

出版信息

Breast. 2009 Oct;18 Suppl 3:S59-63. doi: 10.1016/S0960-9776(09)70275-9.

Abstract

Treatment decisions for breast cancer patients are currently based on a small number of crude predictive markers, despite the known complexity and heterogeneity of the disease. The field of pharmacogenetics can increase the precision with which therapeutic decisions are made. Discovering associations between genetic variation and treatment response will allow clinicians to tailor therapies to most effectively treat that specific tumor in that patient. In this review we outline two genes with potential clinical relevance in breast cancer treatment. A common polymorphism in the gene encoding Fc fragment of IgG low affinity IIIa receptor (FCGR3A; gene: FCGR3A) may substantially influence a patient's likelihood of responding to trastuzumab. The other gene that will be discussed in the review is cytochrome P450 2D6 (CYP2D6; gene: CYP2D6), which has many genetic variants that impair the bioactivation and effectiveness of tamoxifen therapy.

摘要

目前,乳腺癌患者的治疗决策主要基于少数粗略的预测标志物,尽管该疾病的复杂性和异质性是已知的。药物遗传学领域可以提高治疗决策的精确性。发现遗传变异与治疗反应之间的关联将使临床医生能够将治疗方法定制为最有效地治疗该特定肿瘤。在这篇综述中,我们概述了两个在乳腺癌治疗中具有潜在临床相关性的基因。编码 IgG 低亲和力 IIIa 受体 Fc 片段的基因(FCGR3A;基因:FCGR3A)中的常见多态性可能会极大地影响患者对曲妥珠单抗治疗的反应可能性。我们还将在综述中讨论另一个基因细胞色素 P450 2D6(CYP2D6;基因:CYP2D6),它有许多遗传变异会削弱他莫昔芬治疗的生物活化和有效性。

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