Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina.
Cancer Epidemiol Biomarkers Prev. 2017 Dec;26(12):1722-1729. doi: 10.1158/1055-9965.EPI-17-0450. Epub 2017 Sep 13.
African American (AA) women have higher incidence of aggressive, young-onset (<40 years) breast cancers. Young- and older-onset disease may have distinct tumor biologies and etiologies; however, studies investigating age differences among AA women have been rare and generally underpowered. We examined tumor characteristics and breast cancer risk factors associated with premenopausal young (<40) vs. older (≥40) AA women's breast cancer in the African American Breast Cancer Epidemiology and Risk Consortium (2,008 cases and 5,144 controls). Unconditional logistic regression models assessed heterogeneity of tumor biology and risk factor associations by age, overall, and by estrogen receptor status. Premenopausal AA women <40 years had higher frequency of poorer-prognosis tumor characteristics compared with older women, including negative estrogen and progesterone receptor status, triple-negative subtype, higher grade, higher stage, and larger tumors. Adiposity (i.e., waist-to-hip ratio) and family history of breast cancer were more strongly associated with young-onset disease [case-control OR = 1.46, 95% confidence interval (CI) = 1.04-2.05; OR = 3.10, 95% CI = 2.08-4.63, respectively] compared with older-onset disease (OR = 1.11, 95% CI = 0.91-1.35; OR = 1.57, 95% CI = 1.26-1.94). Breastfeeding showed a slight inverse risk association among young women (OR = 0.70, 95% CI = 0.43-1.16). Oral contraceptive use was associated with increased risk regardless of age. Considering various cutoff points for young age (<40, <45, <50), age-related heterogeneity was greatest when <40 was used. Among premenopausal AA women, diagnosis before age 40 is associated with more aggressive breast tumor biology and some etiologic differences. Modifiable risk factors including breastfeeding, adiposity, and oral contraceptive use may be important targets for mitigating harms of young-onset breast cancer. .
非裔美国(AA)女性患有侵袭性、年轻发病(<40 岁)乳腺癌的比例较高。年轻发病和老年发病的肿瘤生物学和病因可能不同;然而,针对 AA 女性年龄差异的研究很少,且通常缺乏效力。我们在非裔美国人乳腺癌流行病学和风险联盟(2008 例病例和 5144 例对照)中研究了绝经前年轻(<40 岁)与老年(≥40 岁)AA 女性乳腺癌相关的肿瘤特征和乳腺癌风险因素。非条件逻辑回归模型评估了按年龄、总体和按雌激素受体状态划分的肿瘤生物学和风险因素相关性的异质性。与老年女性相比,<40 岁的绝经前 AA 女性具有更高频率的预后较差的肿瘤特征,包括雌激素和孕激素受体阴性、三阴性亚型、更高的分级、更高的分期和更大的肿瘤。肥胖(即腰臀比)和乳腺癌家族史与年轻发病的相关性更强[病例对照比值比(OR)=1.46,95%置信区间(CI)=1.04-2.05;OR=3.10,95%CI=2.08-4.63],而与老年发病的相关性较弱(OR=1.11,95%CI=0.91-1.35;OR=1.57,95%CI=1.26-1.94)。母乳喂养在年轻女性中显示出轻微的逆风险关联(OR=0.70,95%CI=0.43-1.16)。无论年龄大小,口服避孕药的使用都与风险增加相关。考虑到年轻年龄(<40、<45、<50)的各种截止点,当使用<40 时,年龄相关性异质性最大。在绝经前的 AA 女性中,<40 岁诊断为乳腺癌与更具侵袭性的乳腺癌肿瘤生物学和一些病因差异有关。可改变的风险因素,包括母乳喂养、肥胖和口服避孕药的使用,可能是减轻年轻发病乳腺癌危害的重要目标。