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
相关论文
共 50 条
  • [31] Impact of CYP2D6 polymorphisms in tamoxifen adjuvant breast cancer treatment
    T. Ramón y Cajal
    A. Altés
    L. Paré
    E. del Rio
    C. Alonso
    A. Barnadas
    M. Baiget
    Breast Cancer Research and Treatment, 2010, 119 : 33 - 38
  • [32] Tamoxifen Metabolite Concentrations, CYP2D6 Genotype, and Breast Cancer Outcomes
    Madlensky, L.
    Natarajan, L.
    Tchu, S.
    Pu, M.
    Mortimer, J.
    Flatt, S. W.
    Nikoloff, D. M.
    Hillman, G.
    Fontecha, M. R.
    Lawrence, H. J.
    Parker, B. A.
    Wu, A. H. B.
    Pierce, J. P.
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2011, 89 (05) : 718 - 725
  • [33] Clinical implications of CYP2D6 genotyping on tamoxifen treatment in breast cancer
    Dezentje, V. O.
    Nortier, J. W. R.
    Guchelaar, H. J.
    van de Velde, C. J. H.
    Gelderblom, H.
    EJC SUPPLEMENTS, 2008, 6 (07): : 56 - 56
  • [34] Clinical Implications of CYP2D6 Genotyping in Tamoxifen Treatment for Breast Cancer
    Dezentje, Vincent O.
    Guchelaar, Henk-Jan
    Nortier, Johan W. R.
    van de Velde, Cornelis J. H.
    Gelderblom, Hans
    CLINICAL CANCER RESEARCH, 2009, 15 (01) : 15 - 21
  • [35] Impact of CYP2D6 polymorphisms in tamoxifen adjuvant breast cancer treatment
    Ramon y Cajal, T.
    Altes, A.
    Pare, L.
    del Rio, E.
    Alonso, C.
    Barnadas, A.
    Baiget, M.
    BREAST CANCER RESEARCH AND TREATMENT, 2010, 119 (01) : 33 - 38
  • [36] Tamoxifen Resistance and CYP2D6 Copy Numbers in Breast Cancer Patients
    Motamedi, Sahar
    Majidzadeh, Keivan
    Mazaheri, Mahta
    Anbiaie, Robab
    Mortazavizadeh, Seyed Mohammad Reza
    Esmaeili, Rezvan
    ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, 2012, 13 (12) : 6101 - 6104
  • [37] Association Between CYP2D6 Polymorphisms and Outcomes Among Women With Early Stage Breast Cancer Treated With Tamoxifen
    Schroth, Werner
    Goetz, Matthew P.
    Hamann, Ute
    Fasching, Peter A.
    Schmidt, Marcus
    Winter, Stefan
    Fritz, Peter
    Simon, Wolfgang
    Suman, Vera J.
    Ames, Matthew M.
    Safgren, Stephanie L.
    Kuffel, Mary J.
    Ulmer, Hans Ulrich
    Bolaender, Julia
    Strick, Reiner
    Beckmann, Matthias W.
    Koelbl, Heinz
    Weinshilboum, Richard M.
    Ingle, James N.
    Eichelbaum, Michel
    Schwab, Matthias
    Brauch, Hiltrud
    JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2009, 302 (13): : 1429 - 1436
  • [38] Influence of CYP2D6 Polymorphisms on Serum Levels of Tamoxifen Metabolites in Spanish Women with Breast Cancer
    Zafra-Ceres, Mercedes
    de Haro, Tomas
    Farez-Vidal, Esther
    Blancas, Isabel
    Bandres, Fernando
    de Duenas, Eduardo Martinez
    Ochoa-Aranda, Enrique
    Gomez-Capilla, Jose A.
    Gomez-Llorente, Carolina
    INTERNATIONAL JOURNAL OF MEDICAL SCIENCES, 2013, 10 (07): : 932 - 937
  • [39] Tamoxifen Benefits and CYP2D6 Testing in Women With Hormone Receptor-Positive Breast Cancer
    Kaplan, Marcelle
    Mahon, Suzanne M.
    CLINICAL JOURNAL OF ONCOLOGY NURSING, 2013, 17 (02) : 174 - 179
  • [40] Optimized CYP2D6 phenotype assignment for plasma endoxifen prediction in breast cancer patients treated with tamoxifen
    Schroth, Werner
    Winter, Stefan
    Eichelbaum, Michel
    Muerdter, Thomas
    Schwab, Matthias
    Brauch, Hiltrud
    CANCER RESEARCH, 2017, 77