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
  • [1] 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
    I Sestak
    R Kealy
    M Nikoloff
    M Fontecha
    J F Forbes
    A Howell
    J Cuzick
    British Journal of Cancer, 2012, 107 : 230 - 233
  • [2] CYP2D6 phenotype, tamoxifen, and risk of contralateral breast cancer in the WECARE Study
    Brooks, Jennifer D.
    Comen, Elizabeth A.
    Reiner, Anne S.
    Orlow, Irene
    Leong, Siok F.
    Liang, Xiaolin
    Mellemkjaer, Lene
    Knight, Julia A.
    Lynch, Charles F.
    John, Esther M.
    Bernstein, Leslie
    Woods, Meghan
    Doody, David R.
    Malone, Kathleen E.
    Bernstein, Jonine L.
    BREAST CANCER RESEARCH, 2018, 20
  • [3] Impact of CYP2D6 Polymorphisms on the Efficacy of Tamoxifen in Iraqi Women With Breast Cancer
    Ali, Sura S. Abid
    Sahib, Ahmed S.
    Abdulamir, Ahmed S.
    Kadhim, Haitham M.
    JOURNAL OF CONTEMPORARY MEDICAL SCIENCES, 2023, 9 (06): : 436 - 448
  • [4] Pharmacogenomics of breast cancer: highlighting CYP2D6 and tamoxifen
    Chan, Carmen W. H.
    Law, Bernard M. H.
    So, Winnie K. W.
    Chow, Ka Ming
    Waye, Mary M. Y.
    JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 2020, 146 (06) : 1395 - 1404
  • [5] Adjusting the dose of tamoxifen in patients with early breast cancer and CYP2D6 poor metabolizer phenotype
    Martinez de Duenas, Eduardo
    Ochoa Aranda, Enrique
    Blancas Lopez-Barajas, Isabel
    Ferrer Magdalena, Teresa
    Bandres Moya, Fernando
    Chicharro Garcia, Luis Miguel
    Gomez Capilla, Jose A.
    Zafra Ceres, Mercedes
    de Haro, Tomas
    Romero Llorens, Regina
    Ferrer Albiach, Carlos
    Ferriols Lisart, Rafael
    Chover Lara, Dolores
    Lopez Rodriguez, Angela
    Munarriz Ferrandis, Javier
    Olmos Anton, Santiago
    BREAST, 2014, 23 (04) : 400 - 406
  • [6] Concurrent use of tamoxifen with CYP2D6 inhibitors and the risk of breast cancer recurrence
    Azoulay, Laurent
    Dell'Aniello, Sophie
    Huiart, Laetitia
    du Fort, Guillaume Galbaud
    Suissa, Samy
    BREAST CANCER RESEARCH AND TREATMENT, 2011, 126 (03) : 695 - 703
  • [7] Impact of CYP2D6 Polymorphisms on Tamoxifen Responses of Women with Breast Cancer: A Microarray-based Study in Thailand
    Sukasem, Chonlaphat
    Sirachainan, Ekaphop
    Chamnanphon, Montri
    Pechatanan, Khunthong
    Sirisinha, Thitiya
    Ativitavas, Touch
    Panvichian, Ravat
    Ratanatharathorn, Vorachai
    Trachu, Narumol
    Chantratita, Wasun
    ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, 2012, 13 (09) : 4549 - 4553
  • [8] Genetic polymorphisms of CYP2D6 increase the risk for recurrence of breast cancer in patients receiving tamoxifen as an adjuvant therapy
    Damodaran, Solai Elango
    Pradhan, Suresh Chandra
    Umamaheswaran, Gurusamy
    Kadambari, Dharanipragada
    Reddy, K. Sathyanarayana
    Adithan, Chandrasekaran
    CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2012, 70 (01) : 75 - 81
  • [9] The CYP2D6*4 polymorphism affects breast cancer survival in tamoxifen users
    Bijl, Monique J.
    van Schaik, Ron H. N.
    Lammers, Laureen A.
    Hofman, Albert
    Vulto, Arnold G.
    van Gelder, Teun
    Stricker, Bruno H. Ch.
    Visser, Loes E.
    BREAST CANCER RESEARCH AND TREATMENT, 2009, 118 (01) : 125 - 130
  • [10] Polymorphism of the CYP2D6 gene in women with breast cancer treated with tamoxifen
    de Vasconcelos-Valenca, R. J.
    Melo, M. A.
    Lima, E. M.
    de Sousa, G. V.
    Nazario, A. C.
    da Silva, B. B.
    EUROPEAN JOURNAL OF GYNAECOLOGICAL ONCOLOGY, 2016, 37 (05) : 700 - 702