Unbound MEDLINE

New-onset breast tenderness after initiation of estrogen plus progestin therapy and breast cancer risk. Archives of internal medicine [Arch Intern Med] Journal article

 
TitleNew-onset breast tenderness after initiation of estrogen plus progestin therapy and breast cancer risk.
Author(s)Crandall CJ, Aragaki AK, Chlebowski RT, McTiernan A, Anderson G, Hendrix SL, Cochrane BB, Kuller LH, Cauley JA 
InstitutionDepartment of Medicine, David Geffen School of Medicine at University of California, UCLA Medicine/GIM, Los Angeles, CA 90024, USA. ccrandall@mednet.ucla.edu
SourceArch Intern Med 2009 Oct 12; 169(18):1684-91.
MeSHAged
Breast
Breast Neoplasms
Estrogen Replacement Therapy
Estrogens, Conjugated (USP)
Female
Humans
Medroxyprogesterone 17-Acetate
Middle Aged
Pain
Postmenopause
Proportional Hazards Models
Sensitivity and Specificity
AbstractBACKGROUND: 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.
Languageeng
Pub Type(s)Journal Article
Randomized Controlled Trial
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
PubMed ID19822825
  
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