Department of Medicine, Section of Epidemiology and Population Sciences, Baylor College of Medicine, Houston, Texas.
Dan L Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, Texas.
Cancer Epidemiol Biomarkers Prev. 2020 Jan;29(1):88-94. doi: 10.1158/1055-9965.EPI-19-1052. Epub 2019 Nov 11.
Incidence rates for hepatocellular carcinoma (HCC) vary considerably by age, sex, and race/ethnicity. We assessed whether the underlying reasons for variations in HCC among subgroups of the population by age, sex, race/ethnicity, and birth cohort are uniform or whether they interact with one another or have changed over time.
Data were from the U.S. Cancer Statistics registry. We assessed annual trends within population subgroups and examined for secular trends in the male-to-female ratio for HCC incidence. We used joinpoint regression to compute annual percent change and average annual percent change (AAPC) and corresponding 95% confidence intervals (CI). We also used age-period-cohort models to disentangle period and cohort effects.
Between 2001 and 2015, HCC rates increased in men and women ≥50 years, remained stable among women ages 40 to 49 years, but decreased among males ages 40 to 44 years (AAPC = -2.47%; 95% CI, -3.15% to -1.80%) and 45 to 49 years (AAPC = -3.49%; 95% CI, -4.78% to -2.17%). As a result, the male-to-female incidence rate ratio (IRR) among persons aged <50 years decreased from 4.63 in 2001 to 2.42 in 2015 but remained stable over time among persons aged ≥50 years. HCC rates were lower among successive cohorts of males born after circa 1956, whereas HCC rates among females born circa 1991 were higher than those among females born circa 1956 (IRR = 1.67; 95% CI, 1.05-2.65).
As a result of decreasing incidence among males aged <50 years and strong cohort effect, the epidemiology of HCC is changing from a disease with striking male predominance to one with less male predominance.
The sex and racial disparities and strong birth cohort effect on HCC risk identified in this study have important implications for population-based HCC prevention efforts.
肝细胞癌(HCC)的发病率因年龄、性别和种族/民族而异。我们评估了人群中按年龄、性别、种族/民族和出生队列划分的 HCC 发病率差异的根本原因是否一致,或者它们是否相互作用或随时间变化。
数据来自美国癌症统计登记处。我们评估了人群亚组内的年度趋势,并检查了 HCC 发病率的男女性别比是否存在长期趋势。我们使用 Joinpoint 回归计算了年度百分比变化和平均年度百分比变化(AAPC)以及相应的 95%置信区间(CI)。我们还使用年龄-时期-队列模型来区分时期和队列效应。
2001 年至 2015 年间,50 岁以上男性和女性的 HCC 发病率上升,40 至 49 岁女性的 HCC 发病率保持稳定,但 40 至 44 岁男性(AAPC=-2.47%;95%CI,-3.15%至-1.80%)和 45 至 49 岁男性(AAPC=-3.49%;95%CI,-4.78%至-2.17%)的 HCC 发病率下降。因此,50 岁以下人群的男性与女性发病率比从 2001 年的 4.63 降至 2015 年的 2.42,但 50 岁以上人群的发病率比保持稳定。出生于 1956 年后的男性的 HCC 发病率逐批降低,而出生于 1991 年的女性的 HCC 发病率高于出生于 1956 年的女性(IRR=1.67;95%CI,1.05-2.65)。
由于 50 岁以下男性发病率下降和强大的队列效应,HCC 的流行病学正在从一种具有明显男性优势的疾病转变为一种男性优势较小的疾病。
本研究确定的 HCC 风险的性别和种族差异以及强大的出生队列效应对基于人群的 HCC 预防工作具有重要意义。