Phthalate Exposure and Breast Cancer Incidence: A Danish Nationwide Cohort Study

Author:

Ahern Thomas P.1,Broe Anne23,Lash Timothy L.45,Cronin-Fenton Deirdre P.5,Ulrichsen Sinna Pilgaard5,Christiansen Peer M.5,Cole Bernard F.1,Tamimi Rulla M.67,Sørensen Henrik Toft5,Damkier Per23

Affiliation:

1. University of Vermont, Burlington, VT

2. University of Southern Denmark, Odense, Denmark

3. Odense University Hospital, Odense, Denmark

4. Emory University, Atlanta, GA

5. Aarhus University Hospital/Randers Regional Hospital, Aarhus, Denmark

6. Brigham and Women’s Hospital, Boston, MA

7. Harvard T.H. Chan School of Public Health, Boston, MA

Abstract

PURPOSE Phthalate exposure is ubiquitous and especially high among users of drug products formulated with phthalates. Some phthalates mimic estradiol and may promote breast cancer. Existing epidemiologic studies on this topic are small, mostly not prospective, and have given inconsistent results. We estimated associations between longitudinal phthalate exposures and breast cancer risk in a Danish nationwide cohort, using redeemed prescriptions for phthalate-containing drug products to measure exposure. METHODS We ascertained the phthalate content of drugs marketed in Denmark using an internal Danish Medicines Agency ingredient database. We enrolled a Danish nationwide cohort of 1.12 million women at risk for a first cancer diagnosis on January 1, 2005. By combining drug ingredient data with the Danish National Prescription registry, we characterized annual, cumulative phthalate exposure through redeemed prescriptions. We then fit multivariable Cox regression models to estimate associations between phthalate exposures and incident invasive breast carcinoma according to tumor estrogen receptor status. RESULTS Over 9.99 million woman-years of follow-up, most phthalate exposures were not associated with breast cancer incidence. High-level dibutyl phthalate exposure (≥ 10,000 cumulative mg) was associated with an approximately two-fold increase in the rate of estrogen receptor–positive breast cancer (hazard ratio, 1.9; 95% CI, 1.1 to 3.5), consistent with in vitro evidence for an estrogenic effect of this compound. Lower levels of dibutyl phthalate exposure were not associated with breast cancer incidence. CONCLUSION Our results suggest that women should avoid high-level exposure to dibutyl phthalate, such as through long-term treatment with pharmaceuticals formulated with dibutyl phthalate.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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