Infections and Immunoepidemiology Branch, Division of Cancer Epidemiology and Genetics (DCEG), National Cancer Institute, Bethesda, MD 20852, USA.
Int J Cancer. 2010 Apr 1;126(7):1732-9. doi: 10.1002/ijc.24934.
Burkitt lymphoma (BL) is a unique B-cell non-Hodgkin lymphoma with 3 established clinical-epidemiological variants: endemic, sporadic and AIDS-related BL. BL variants show characteristic dysregulation of MYC gene, but the causes of MYC dysregulation or BL arising at different ages are poorly understood. Therefore, we examined population-based BL incidence patterns in the United States to determine age-related risk. BL case and population data were obtained from the NCI's Surveillance, Epidemiology and End Results Databases (1973-2005). Standard cross-sectional age-standardized and age-specific incidence rates were stratified by sex and race and supplemented with age-period-cohort models. We analyzed 3,058 BL cases diagnosed during 1,160,300,297 person-years of observation. Age-standardized incidence rates rose 6.8% per year (95% CI 4.5-9.1) for males and 7.1% (95% CI 3.2-11.1) for females during the study period. The rate among males was 3.2 times that among females, and among Whites 1.3 times that among Blacks. Male-to-female incidence rate ratios did not differ by race, but were 4.2 for pediatric (0-19 years), 4.1 for adult (20-59 years) and 2.0 for geriatric (> or = 60 years) BL. Cross-sectional age-specific rates showed 2 separate peaks among males and females, near ages 10 and 75 years, and a 3rd peak near age 40 years among males. The tri/bimodal incidence pattern was present in sensitivity analyses excluding registries with many HIV/AIDS cases and in period-specific, cohort-specific analyses. To our knowledge, tri/bimodal incidence patterns have not previously been reported for BL. Trimodal/bimodal BL suggests heterogeneity in etiology or biology of BL diagnosed at different ages in males and females.
伯基特淋巴瘤(BL)是一种独特的 B 细胞非霍奇金淋巴瘤,有 3 种已确立的临床-流行病学变异型:地方性、散发性和艾滋病相关 BL。BL 变异型表现出 MYC 基因的特征性失调,但 MYC 失调的原因或不同年龄发生的 BL 原因尚不清楚。因此,我们检查了美国基于人群的 BL 发病率模式,以确定与年龄相关的风险。BL 病例和人口数据来自 NCI 的监测、流行病学和最终结果数据库(1973-2005 年)。按性别和种族对标准横断面年龄标准化和年龄特异性发病率进行分层,并补充年龄-时期-队列模型。我们分析了在 1160300297 人年的观察中诊断出的 3058 例 BL 病例。在研究期间,男性的年龄标准化发病率每年上升 6.8%(95%CI 4.5-9.1),女性每年上升 7.1%(95%CI 3.2-11.1)。男性的发病率是女性的 3.2 倍,白人是黑人的 1.3 倍。男性与女性的发病率比率不因种族而异,但儿科(0-19 岁)为 4.2,成人(20-59 岁)为 4.1,老年(≥60 岁)为 2.0。横断面年龄特异性率显示男性和女性各有 2 个单独的高峰,接近 10 岁和 75 岁,男性接近 40 岁时有第 3 个高峰。这种三/双峰发病率模式在排除了许多 HIV/AIDS 病例的登记处的敏感性分析中以及在特定时期、特定队列的分析中均存在。据我们所知,BL 以前没有报道过三/双峰发病率模式。三/双峰 BL 表明男性和女性不同年龄诊断的 BL 在病因或生物学上存在异质性。