Stroke risk and tamoxifen therapy for breast cancer

被引:31
作者
Geiger, AM
Fischberg, GM
Chen, WS
Bernstein, L
机构
[1] Kaiser Permanente So Calis, Res & Evaluat Dept, Pasadena, CA 91188 USA
[2] Univ So Calif, Sch Med, Dept Neurol, Los Angeles, CA 90033 USA
[3] Univ So Calif, Keck Sc Med, Dept Prevent Med, Los Angeles, CA 90033 USA
来源
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE | 2004年 / 96卷 / 20期
关键词
D O I
10.1093/jnci/djh285
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Tamoxifen, which is used widely to treat, and increasingly to prevent, breast cancer, has been associated with increased risk of stroke. We assessed the impact of tamoxifen treatment for breast cancer on the risk of stroke, considering dose, duration, and recency of use of tamoxifen and known stroke risk factors. Methods: We conducted a nested case-control study of stroke after breast cancer among female Los Angeles County residents enrolled in a large health maintenance organization when diagnosed with breast cancer between January 1, 1980, and July 1, 2000. We obtained information on breast cancer treatment and stroke risk factors through medical record review and telephone interviews. The association (odds ratio [OR] and 95% confidence interval [Cl]) between tamoxifen and stroke risk was determined by using a conditional logistic regression model, adjusting for menopausal status and history of hypertension and diabetes. All statistical tests were two-sided. Results: Of 11 045 women with breast cancer, 179 met stroke eligibility criteria and were individually matched to two stroke-free control subjects with breast cancer on age and year of breast cancer diagnosis. The mean age at breast cancer diagnosis was 66.6 years (standard deviation [SD] = 12.3 years), and the mean at-risk period (i.e., the time between breast cancer diagnosis and first stroke or comparable time period for control subjects) was 5.7 years (SD = 4.5 years). Tamoxifen use was not associated with risk of stroke, either overall (OR = 1.0, 95% CI = 0.6 to 1.6) or in subgroups defined by duration, dose, or recency of use. Chemotherapy, but not a specific chemotherapy regimen, was associated with an increased risk of stroke, regardless of tamoxifen use (no tamoxifen use, OR = 2.8, 95% CI = 1.3 to 6.3; tamoxifen use OR = 2.2, 95% CI = 1.2 to 4.1). Conclusions: Tamoxifen use is not associated with increased stroke risk. Further exploration of possible increased stroke risk following chemotherapy treatment for breast cancer is needed.
引用
收藏
页码:1528 / 1536
页数:9
相关论文
共 30 条
[1]  
Abe O, 1998, LANCET, V352, P930
[2]  
[Anonymous], 1988, J CLIN EPIDEMIOL, V41, P105, DOI DOI 10.1016/0895-4356(88)90084-4
[3]   Raloxifene and cardiovascular events in osteoporotic postmenopausal women - Four-year results from the MORE (Multiple Outcomes of Raloxifene Evaluation) randomized trial [J].
Barrett-Connor, E ;
Grady, D ;
Sashegyi, A ;
Anderson, PW ;
Cox, DA ;
Hoszowski, K ;
Rautaharju, P ;
Harper, KD .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 287 (07) :847-857
[4]  
BRESLOW NE, 1980, IARC SCI PUBL, V32, P192
[5]   Risk of stroke in women exposed to low-dose oral contraceptives - A critical evaluation of the evidence [J].
Chan, WS ;
Ray, J ;
Wai, EK ;
Ginsburg, S ;
Hannah, ME ;
Corey, PN ;
Ginsberg, JS .
ARCHIVES OF INTERNAL MEDICINE, 2004, 164 (07) :741-747
[6]  
Clarke M, 1998, LANCET, V351, P1451
[7]   Hypercoagulable state in patients with advanced gastrointestinal cancer: Evidence for an acquired resistance to activated protein C [J].
De Lucia, D ;
De Vita, F ;
Orditura, M ;
Renis, V ;
Belli, A ;
Conte, M ;
di Grazia, M ;
Iacoviello, L ;
Donati, MB ;
Catalano, G .
TUMORI, 1997, 83 (06) :948-952
[8]   Occurrence of stroke with tamoxifen in NSABP B-24 [J].
Dignam, JJ ;
Fisher, B .
LANCET, 2000, 355 (9206) :848-849
[9]  
*EARL BREAST CANC, 2004, COCHR DAT SYST REV
[10]  
EISEN A, 2003, P ASCO, V22, P98