1 University of Vermont, Burlington, VT.
2 University of Southern Denmark, Odense, Denmark.
J Clin Oncol. 2019 Jul 20;37(21):1800-1809. doi: 10.1200/JCO.18.02202. Epub 2019 Apr 17.
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.
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.
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.
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.
邻苯二甲酸酯暴露普遍存在,尤其是在使用含有邻苯二甲酸酯的药物产品的使用者中。一些邻苯二甲酸酯模拟雌二醇,可能促进乳腺癌。关于这个主题的现有流行病学研究规模较小,大多不是前瞻性的,结果不一致。我们使用含有邻苯二甲酸酯的药物产品的处方兑换来衡量暴露情况,在丹麦全国队列中估计了邻苯二甲酸酯暴露与乳腺癌风险之间的纵向关联。
我们使用丹麦内部药品管理局成分数据库确定在丹麦销售的药物中的邻苯二甲酸酯含量。我们招募了 112 万丹麦全国范围内有患第一癌症风险的女性队列,于 2005 年 1 月 1 日入组。通过将药物成分数据与丹麦国家处方登记处相结合,我们根据处方兑换情况描述了每年、累积的邻苯二甲酸酯暴露情况。然后,我们拟合多变量 Cox 回归模型,根据肿瘤雌激素受体状态估计邻苯二甲酸酯暴露与侵袭性乳腺癌发病之间的关联。
在超过 999 万妇女年的随访期间,大多数邻苯二甲酸酯暴露与乳腺癌发病率无关。高水平的邻苯二甲酸二丁酯暴露(≥10000 毫克累积)与雌激素受体阳性乳腺癌的发生率增加约两倍相关(危险比,1.9;95%置信区间,1.1 至 3.5),这与该化合物具有雌激素作用的体外证据一致。较低水平的邻苯二甲酸二丁酯暴露与乳腺癌发病率无关。
我们的结果表明,女性应避免高水平的邻苯二甲酸二丁酯暴露,例如通过长期使用含有邻苯二甲酸二丁酯的药物治疗。