Inherited and acquired risk factors for venous thromboembolic disease among women taking tamoxifen to prevent breast cancer

被引:69
作者
Duggan, C
Marriott, K
Edwards, R
Cuzick, J
机构
[1] Wolfson Inst Prevent Med, Dept Epidemiol Math & Stat, London EC1M 6BQ, England
[2] St Marys NHS Trust, Dept Haematol, London, England
关键词
D O I
10.1200/JCO.2003.10.111
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Venous thromboembolism (VTE) is of particular concern in women receiving tamoxifen in a chemopreventive setting. We investigate the association between acquired and inherited risk factors for VTE in the International Breast Cancer Intervention Study (IBIS-I) trial of tamoxifen prophylaxis for women at increased risk of breast cancer. Methods: We used a nested case-control study design to investigate the role of tamoxifen and acquired risk factors in the risk of developing a VTE. Results: Tamoxifen was associated with a significantly increased risk of developing a major VTE (odds ratio [OR], 2.1; 95% CI, 1.1 to 4.1). Women who had surgery, immobilization, or fracture in the previous month had a greatly increased risk of developing a major VTE (OR, 4.7, 95% CI, 2.2 to 10.1). Prothrombin and factor V Leiden mutations were found exclusively among control women: factor V Leiden in eight of 159 control women (5.0%) and the prothrombin mutation in three control women (1.9%). Thirty-five women with a VTE and a blood sample were negative for these mutations. The upper one-sided 97.5% CI for the OR of having either mutation was 1.87. Being overweight, smoking, or taking hormone replacement therapy was not associated with VTE in this study, but the CIs were wide. Conclusion: Tamoxifen and prior surgery, fracture, or immobilization were associated with a significantly increased risk of developing a VTE. Factor V Leiden and prothrombin mutations were not associated with thrombosis in this population. (C) 2003 by American Society of Clinical Oncology.
引用
收藏
页码:3588 / 3593
页数:6
相关论文
共 44 条
[1]  
Baum M, 2002, LANCET, V359, P2131
[2]   MUTATION IN BLOOD-COAGULATION FACTOR-V ASSOCIATED WITH RESISTANCE TO ACTIVATED PROTEIN-C [J].
BERTINA, RM ;
KOELEMAN, BPC ;
KOSTER, T ;
ROSENDAAL, FR ;
DIRVEN, RJ ;
DERONDE, H ;
VANDERVELDEN, PA ;
REITSMA, PH .
NATURE, 1994, 369 (6475) :64-67
[3]   ENHANCEMENT BY FACTOR-V LEIDEN MUTATION OF RISK OF DEEP-VEIN THROMBOSIS ASSOCIATED WITH ORAL-CONTRACEPTIVES CONTAINING 3RD-GENERATION PROGESTAGEN [J].
BLOEMENKAMP, KWM ;
ROSENDAAL, FR ;
HELMERHORST, FM ;
BULLER, HR ;
VANDENBROUCKE, JP .
LANCET, 1995, 346 (8990) :1593-1596
[4]   The G20210A mutation of the prothrombin gene in patients with previous first episodes of deep-vein thrombosis: Prevalence and association with factor V G1691A, methylenetetrahydrofolate reductase C677T and plasma prothrombin levels [J].
Cattaneo, M ;
Chantarangkul, V ;
Taioli, E ;
Santos, JH ;
Tagliabue, L .
THROMBOSIS RESEARCH, 1999, 93 (01) :1-8
[5]   Effect of tamoxifen on venous thrombosis risk factors in women without cancer: the Breast Cancer Prevention Trial [J].
Cushman, M ;
Costantino, JP ;
Bovill, EG ;
Wickerham, DL ;
Buckley, L ;
Roberts, JD ;
Krag, DN .
BRITISH JOURNAL OF HAEMATOLOGY, 2003, 120 (01) :109-116
[6]  
Cuzick J, 2002, LANCET, V360, P817
[7]   Overview of the main outcomes in breast-cancer prevention trials [J].
Cuzick, J ;
Powles, T ;
Veronesi, U ;
Forbes, J ;
Edwards, R ;
Ashley, S ;
Boyle, P .
LANCET, 2003, 361 (9354) :296-300
[8]   Risk of venous thromboembolism in users of hormone replacement therapy [J].
Daly, E ;
Vessey, MP ;
Hawkins, MN ;
Carson, JL ;
Gough, P ;
Marsh, S .
LANCET, 1996, 348 (9033) :977-980
[9]  
de Moerloose P, 1998, THROMB HAEMOSTASIS, V80, P239
[10]   Venous thromboembolism following major orthopedic surgery: Review of epidemiology and economics [J].
Edelsberg, J ;
Ollendorf, D ;
Oster, G .
AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY, 2001, 58 (21) :S4-S13