Mullooly Maeve, Murphy Jeanne, Gierach Gretchen L, Walsh Paul M, Deady Sandra, Barron Thomas I, Sherman Mark E, Rosenberg Philip S, Anderson William F
Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA; Cancer Prevention Fellowship Program, Division of Cancer Prevention, National Cancer Institute, Bethesda, MD, USA.
George Washington University School of Nursing, Washington, DC, USA.
Eur J Cancer. 2017 Nov;86:326-333. doi: 10.1016/j.ejca.2017.08.031. Epub 2017 Oct 23.
The aetiology and clinical behaviour of breast cancers vary by oestrogen receptor (ER) expression, HER2 expression and over time. Data from the United States and Denmark show rising incidence rates for ER+ and falling incidence rates for ER- breast cancers. Given that Ireland is a somewhat similar Western population but with distinctive risk exposures (especially for lactation), we analysed breast cancer trends by ER status; and for the first time, by the joint expression of ER±/HER2±. We assessed invasive breast cancers (n = 24,845; 2004-2013) within the population-based National Cancer Registry of Ireland. The population at risk was obtained from the Irish Central Statistics Office (n = 10,401,986). After accounting for missing ER and HER2 data, we assessed receptor-specific secular trends in age-standardised incidence rates (ASRs) with the estimated annual percentage change (EAPC) and corresponding 95% confidence intervals (95% CI). Age-period-cohort models were also fitted to further characterise trends accounting for age, calendar-period and birth-cohort interactions. ASRs increased for ER+ (EAPC: 2.2% per year [95% CI: 0.97, 3.45%/year]) and decreased for ER- cancers (EAPC: -3.43% per year [95% CI: -5.05, -1.78%/year]), as well as for specific age groups at diagnosis (<30-49, 50-64 and ≥65 years). ER+/HER2- cancers rose, ER+/HER2+ cancers were statistically flat and ER-/HER± cancers declined. Secular trends for ER± cancers in Ireland were like those previously observed. Stratification by HER2± expression did not substantively alter ER± trends. The divergence of ER± incidence rates among independent Western populations likely reflects calendar-period and/or risk factor changes with differential effects for ER+ and ER- breast cancers.
乳腺癌的病因和临床行为因雌激素受体(ER)表达、HER2表达以及时间的不同而有所差异。来自美国和丹麦的数据显示,ER阳性乳腺癌的发病率呈上升趋势,而ER阴性乳腺癌的发病率则呈下降趋势。鉴于爱尔兰是一个与之类似的西方人群,但有独特的风险暴露因素(尤其是哺乳期),我们按ER状态分析了乳腺癌的发病趋势;并且首次按ER±/HER2±的联合表达进行了分析。我们评估了爱尔兰基于人群的国家癌症登记处内的浸润性乳腺癌(n = 24,845;2004 - 2013年)。有风险的人群数据来自爱尔兰中央统计局(n = 10,401,986)。在考虑了缺失的ER和HER2数据后,我们用估计的年百分比变化(EAPC)和相应的95%置信区间(95%CI)评估了年龄标准化发病率(ASR)中受体特异性的长期趋势。还拟合了年龄 - 时期 - 队列模型,以进一步描述考虑年龄、日历时期和出生队列相互作用后的趋势。ER阳性乳腺癌的ASR上升(EAPC:每年2.2% [95%CI:0.97,3.45%/年]),ER阴性癌症的ASR下降(EAPC:每年 - 3.43% [95%CI: - 5.05, - 1.78%/年]),以及诊断时的特定年龄组(<30 - 49岁、50 - 64岁和≥65岁)也是如此。ER+/HER2 - 癌症上升,ER+/HER2+癌症在统计学上无变化,ER - /HER±癌症下降。爱尔兰ER±癌症的长期趋势与之前观察到的相似。按HER2±表达分层并没有实质性改变ER±趋势。独立西方人群中ER±发病率的差异可能反映了日历时期和/或风险因素的变化,对ER阳性和ER阴性乳腺癌有不同的影响。