Clinical and biomarker predictors of side effects from tamoxifen

被引:114
作者
Lorizio, Wendy [1 ,2 ,3 ,4 ]
Wu, Alan H. B. [5 ,6 ]
Beattie, Mary S. [2 ,4 ,7 ,8 ,9 ]
Rugo, Hope [4 ,9 ,10 ]
Tchu, Simone [6 ,11 ]
Kerlikowske, Karla [12 ,13 ]
Ziv, Elad [1 ,2 ,4 ,7 ,8 ]
机构
[1] UCSF Helen Diller Family Canc Res Bldg, San Francisco, CA 94158 USA
[2] Univ Calif San Francisco, Dept Med, Div Gen Internal Med, San Francisco, CA USA
[3] Univ Calif San Francisco, Dept Med, Div Clin Pharmacol & Expt Therapeut, San Francisco, CA USA
[4] Univ Calif San Francisco, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Dept Lab Med, San Francisco, CA 94143 USA
[6] San Francisco Gen Hosp, San Francisco, CA 94110 USA
[7] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
[8] Univ Calif San Francisco, Inst Human Genet, San Francisco, CA 94143 USA
[9] UCSF Med Ctr Mt Zion, San Francisco, CA 94143 USA
[10] Univ Calif San Francisco, Dept Med, Div Hematol & Oncol, San Francisco, CA USA
[11] Univ Calif San Francisco, Dept Biopharmaceut Sci, San Francisco, CA 94143 USA
[12] San Francisco VA Med Ctr, Div Gen Internal Med, San Francisco, CA 94121 USA
[13] Univ Calif San Francisco, Dept Med & Epidemiol & Biostat, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
Tamoxifen; Side effects; Predictors; Biomarkers; Endoxifen; Breast cancer treatment; QUALITY-OF-LIFE; SURGICAL ADJUVANT BREAST; HOT FLASHES; CYP2D6; GENOTYPE; ESTROGEN-RECEPTOR; CANCER PREVENTION; JAPANESE-AMERICAN; RISK-FACTORS; SYMPTOMS; METABOLITE;
D O I
10.1007/s10549-011-1893-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tamoxifen decreases breast cancer recurrence, mortality, and breast cancer risk in high-risk women. Despite these proven benefits, tamoxifen use is often limited due to side effects. We identified predictors of tamoxifen-induced side effects based on clinical variables and serum tamoxifen metabolite biomarkers in a cross-sectional study of patients taking tamoxifen. We enrolled 241 women and collected data on demographics, tamoxifen use and side effects, as well as potential clinical and serum predictors. We used logistic regression models and adjusted for age, body mass index, ethnicity, education, prior post-menopausal hormone therapy (HT), tamoxifen duration, and endoxifen levels to identify factors associated with side effects. Common tamoxifen attributed side effects were hot flashes (64%), vaginal dryness (35%), sleep problems (36%), weight gain (6%), and depression, irritability or mood swings (6%). In multi-variate models, tamoxifen duration, age, prior post-menopausal HT, and endoxifen levels all predicted side effects. Women who had been on tamoxifen for > 12 months were less likely to report side effects (OR 0.15, 95% CI 0.04-0.58) or severe side effects (OR 0.05, 95% CI 0.005-0.58) compared to women on tamoxifen for < 12 months. Compared to women younger than 50, women who were age 60-70 and older than 70 were less likely to report side effects (OR 0.22, 95% CI 0.03-1.35; OR 0.13, 95% CI 0.01-0.99; respectively). Women who previously took post-menopausal HT were more likely to report severe side effects. Women with higher endoxifen levels were more likely to report side effects (OR 1.67, 95% CI 1.01-2.77 per standard deviation increase in endoxifen). Clinicians should consider closely monitoring adherence in women taking tamoxifen, especially in younger women, and women who previously took HT. The association between endoxifen levels and side effects is consistent with the data that suggest that endoxifen is the most highly active metabolite of tamoxifen.
引用
收藏
页码:1107 / 1118
页数:12
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