Relationships between CYP2D6 phenotype, breast cancer and hot flushes in women at high risk of breast cancer receiving prophylactic tamoxifen: results from the IBIS-I trial

被引:18
|
作者
Sestak, I. [1 ]
Kealy, R. [1 ]
Nikoloff, M. [2 ]
Fontecha, M. [2 ]
Forbes, J. F. [3 ]
Howell, A. [4 ]
Cuzick, J. [1 ]
机构
[1] Queen Mary Univ London, Wolfson Inst Prevent Med, Ctr Canc Prevent, London EC1M 6BQ, England
[2] Roche Mol Syst Inc, Pleasanton, CA 94588 USA
[3] Univ Newcastle, Sch Med Practice & Populat Hlth, Newcastle, NSW 2308, Australia
[4] Univ Hosp S Manchester Wythenshawe I, Genesis Prevent Ctr, Manchester M23 9LT, Lancs, England
关键词
breast cancer; CYP2D6; polymorphism; tamoxifen; hot flushes; ADJUVANT TAMOXIFEN; PREVENTION TRIAL; GENOTYPE; RECURRENCE; FLASHES; ASSOCIATION; METABOLISM; SURVIVAL; CYP2D6-ASTERISK-10; BIOTRANSFORMATION;
D O I
10.1038/bjc.2012.278
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Several studies have reported discordant results regarding the impact of the CYP2D6 phenotype on both the effectiveness and the degree of endocrine symptoms associated with tamoxifen. Other studies have suggested that menopausal symptoms may be a predictive factor to tamoxifen response. METHODS: We investigated the relationship between the CYP2D6-predicted phenotype and tamoxifen response in a nested case-control study among women from the International Breast cancer Intervention Study (IBIS-I), which evaluated tamoxifen in the preventive setting. RESULTS: In this retrospective analysis of the tamoxifen-treated women in the IBIS-I study, 9 women (16.6%) who developed oestrogen receptor-positive invasive breast cancer had a 2D6 poor or intermediate metaboliser phenotype compared with 45 (20.6%) controls. Adjusted matched logistic regression revealed no significant difference between cases and controls for extensive vs intermediate metaboliser phenotype (OR=0.81 (0.30-2.23), P=0.7) or extensive vs poor metaboliser phenotype (OR=1.02 (0.31-3.32), P=0.9). Controls in the tamoxifen group with a poor metaboliser phenotype developed nonsignificantly fewer hot flushes compared with those with an extensive metaboliser phenotype (OR=0.40 (0.12-1.31)), but those with the intermediate phenotype developed nonsignificantly more hot flushes (OR=1.38 (0.58-3.29)) in an unadjusted analysis. CONCLUSION: Data from the preventive IBIS-I study did not support an association between the CYP2D6 phenotype and breast cancer outcome or the development of endocrine symptoms in tamoxifen-treated women. British Journal of Cancer (2012) 107, 230-233. doi:10.1038/bjc. 2012.278 www.bjcancer.com Published online 26 June 2012 (c) 2012 Cancer Research UK
引用
收藏
页码:230 / 233
页数:4
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