Tamoxifen, hot flashes and recurrence in breast cancer

被引:0
作者
Joanne E. Mortimer
Shirley W. Flatt
Barbara A. Parker
Ellen B. Gold
Linda Wasserman
Loki Natarajan
John P. Pierce
机构
[1] University of California,Cancer Prevention and Control Program, Moores UCSD Cancer Center
[2] University of California,Department of Public Health Sciences
[3] Davis,undefined
来源
Breast Cancer Research and Treatment | 2008年 / 108卷
关键词
Breast cancer; Hot flashes; Survival; Tamoxifen;
D O I
暂无
中图分类号
学科分类号
摘要
We utilized data from the comparison group of the Women’s Healthy Eating and Living randomized trial to investigate an “a priori” hypothesis suggested by CYP2D6 studies that hot flashes may be an independent predictor of tamoxifen efficacy. A total of 1551 women with early stage breast cancer were enrolled and randomized to the comparison group of the WHEL multi-institutional trial between 1995 and 2000. Their primary breast cancer diagnoses were between 1991 and 2000. At study entry, 864 (56%) of these women were taking tamoxifen, and hot flashes were reported by 674 (78%). After 7.3 years of follow-up, 127 of those who took tamoxifen at baseline had a confirmed breast cancer recurrence. Women who reported hot flashes at baseline were less likely to develop recurrent breast cancer than those who did not report hot flashes (12.9% vs 21%, P = 0.01). Hot flashes were a stronger predictor of breast cancer specific outcome than age, hormone receptor status, or even the difference in the stage of the cancer at diagnosis (Stage I versus Stage II). These findings suggest an association between side effects, efficacy, and tamoxifen metabolism. The strength of this finding suggests that further study of the relationship between hot flashes and breast cancer progression is warranted. Additional work is warranted to clarify the mechanism of hot flashes in this setting.
引用
收藏
页码:421 / 426
页数:5
相关论文
共 48 条
[1]  
Stearns V(2003)Active tamoxifen metabolite plasma concentrations after coadministration of tamoxifen and the selective serotonin reuptake inhibitor paroxetine J Natl Cancer Inst 95 1758-1764
[2]  
Johnson MD(2006)Quantitative effect of CYP2D6 genotype and inhibitors on tamoxifen metabolism: implication for optimization of breast cancer treatment Clin Pharmacol Ther 80 61-74
[3]  
Rae JM(2004)Comprehensive evaluation of tamoxifen sequential biotransformation by the human cytochrome P450 system in vitro: prominent roles for CYP3A and CYP2D6 J Pharmacol Exp Ther 310 1062-1075
[4]  
Borges S(2005)Pharmacogenetics of tamoxifen biotransformation is associated with clinical outcomes of efficacy and hot flashes J Clin Oncol 23 9312-9318
[5]  
Desta Z(2002)Estrogen raises the sweating threshold in postmenopausal women with hot flashes Fertil Steril 77 487-490
[6]  
Li L(2002)Hot flushes Lancet 360 1851-1861
[7]  
Desta Z(1990)Hot flashes: epidemiology and physiology Ann NY Acad Sci 592 52-86; discussion 123–133
[8]  
Ward BA(1998)Hot flashes in postmenopausal women treated for breast carcinoma: prevalence, severity, correlates, management, and relation to quality of life Cancer 82 1682-1691
[9]  
Soukhova NV(1995)Prevalence of menopausal symptoms among women with a history of breast cancer and attitudes toward estrogen replacement therapy J Clin Oncol 13 2737-2744
[10]  
Goetz MP(2005)A universal menopausal syndrome? Am J Med 118 37-46