TY  - JOUR
T1  - NEw-onset breast tenderness after initiation of estrogen plus progestin therapy and breast cancer risk
AU  - Crandall CJ, Aragaki AK, Chlebowski RT, et al
Y1  - 2009/10/12
N1  - 10.1001/archinternmed.2009.303
JO  - Archives of Internal Medicine
SP  - 1684
EP  - 1691
VL  - 169
IS  - 18
N2  - Background 
    Estrogen plus progestin therapy increases breast cancer incidence and breast tenderness. Whether breast tenderness during estrogen plus progestin therapy is associated with breast cancer risk is uncertain.Methods 
    We analyzed data from the Women's Health Initiative Estrogen + Progestin Trial, which randomized postmenopausal women with an intact uterus to receive daily conjugated equine estrogens, 0.625 mg, plus medroxyprogesterone acetate, 2.5 mg (n = 8506), or placebo (n = 8102). At baseline and annually, participants underwent mammography and clinical breast examination. Self-reported breast tenderness was assessed at baseline and at 12 months. The incidence of invasive breast cancer was confirmed by medical record review (mean follow-up of 5.6 years).Results 
    Of women without baseline breast tenderness (n = 14 538), significantly more assigned to receive conjugated equine estrogens plus medroxyprogesterone vs placebo experienced new-onset breast tenderness after 12 months (36.1% vs 11.8%, P < .001). Of women in the conjugated equine estrogens plus medroxyprogesterone group, breast cancer risk was significantly higher in those with new-onset breast tenderness compared with those without (hazard ratio, 1.48; 95% confidence interval, 1.08-2.03; P = .02). In the placebo group, breast cancer risk was not significantly associated with new-onset breast tenderness (P = .97).Conclusions 
    New-onset breast tenderness during conjugated equine estrogens plus medroxyprogesterone therapy was associated with increased breast cancer risk. The sensitivity and specificity of the association between breast tenderness and breast cancer were similar in magnitude to those of the Gail model.Trial Registration 
    clinicaltrials.gov Identifier: NCT00000611
SN  - 0003-9926
M3  - doi: 10.1001/archinternmed.2009.303
UR  - http://dx.doi.org/10.1001/archinternmed.2009.303
ER  -