Impact of CYP2D6 polymorphism on tamoxifen therapy: where are we?Bedeutung des CYP2D6 Polymorphismus für die Tamoxifen Therapie: eine Standortbestimmung

被引:0
作者
Ariana E. Huber-Wechselberger
Paul Niedetzky
Irene Aigner
Elisabeth Haschke-Becher
机构
[1] Elisabethinen Hospital Linz GmbH,Competence Center of Molecular Biology and Genetics
[2] Elisabethinen Hospital Linz GmbH,Institute of Medical and Laboratory Diagnostics
[3] Paracelsus Medical University Salzburg,Central Laboratory, Christian Doppler Hospital Salzburg
关键词
CYP2D6; Tamoxifen; Breast cancer; Pharmacogenetics; CYP2D6; Tamoxifen; Brustkrebs; Pharmakogenetik;
D O I
10.1007/s10354-012-0118-8
中图分类号
学科分类号
摘要
Tamoxifen is a mainstay in the treatment of hormone-receptor sensitive breast cancer. To be effective, it needs conversion into 4-hydroxy-tamoxifen and endoxifen. The key enzyme involved is encoded by the gene CYP2D6 of which several, sometimes population-specific alleles are known. Corresponding enzyme variants may result in poor, intermediate, and extensive metabolization and therefore different steady-state plasma levels of active metabolites. Those are hypothesized to be linked to clinical outcomes of tamoxifen therapy. However, a wealth of mostly retrospective cohort studies came up with conflicting results. Appraisal of these studies is difficult and a metaanalysis impossible due to heterogeneity of patient populations, disease factors, treatment modalities, and measured outcomes. As standardization would not overcome intrinsic limitations of retrospective analyses, prospective trials comparing genotype-guided versus unsighted tamoxifen treatment are required to prove whether routine CYP2D6 genotyping is clinically effective and cost-effective.
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页码:252 / 261
页数:9
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