Laboratory of Epidemiology, Radioprotection and Nuclear Safety Institute, Fontenay aux Roses, France.
Radiation Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.
Cancer. 2019 Jul 15;125(14):2497-2505. doi: 10.1002/cncr.32125. Epub 2019 Apr 23.
Pediatric differentiated thyroid cancer (DTC) rates have increased over time in the United States and worldwide. Improvements in imaging for the diagnosis of DTC have been hypothesized as a potential driver of these increases. This study stratifies temporal trends in pediatric DTC by stage and tumor size to assess whether rates of large, late-stage cancers, which are likely to be clinically meaningful, are increasing over time.
Age-standardized incidence rates (ASRs) of DTC and annual percent changes (APCs) in primary DTC rates were estimated for 0- to 19-year-olds with data from 39 US cancer registries during 1998-2013.
During 1998-2013, 7296 cases of DTC were diagnosed (6652 papillary cases and 644 follicular cases). APCs of pediatric DTCs significantly increased by 4.43%/y [95% CI, 3.74%/y-5.13%/y], primarily because of increases in papillary histologies. Increasing trends were observed for children aged 10 to 19 years for both sexes and for non-Hispanic whites, non-Hispanic blacks, and Hispanics. Rates increased significantly over the time period for all tumor stages (APC , +4.06%/y [95% CI, 2.84%/y-5.29%/y]; APC , +5.68%/y [95% CI, 4.64%/y-6.73%/y]; APC , +8.55%/y [95% CI, 5.03%/y-12.19%/y]) and across tumor sizes (APC , +9.46%/y [95% CI, 6.13%/y-12.90%/y]; APC , +6.92%/y [95% CI, 4.31%/y-9.60%/y]; APC , +4.69%/y [95% CI, 2.75%/y-6.67%/y]).
Significantly increasing rates of DTC over time among 10- to 19-year-olds in the United States are unlikely to be entirely explained by increases in medical surveillance during childhood because rates of large and late-stage DTC are increasing over time. Future studies should examine environmental and other factors that may be contributing to rising DTC rates.
在美国和全球范围内,小儿分化型甲状腺癌(DTC)的发病率随时间推移而增加。人们假设,DTC 诊断成像的改进可能是导致这些增加的一个潜在驱动因素。本研究通过分期和肿瘤大小对小儿 DTC 的时间趋势进行分层,以评估可能具有临床意义的大型晚期癌症的发生率是否随时间推移而增加。
使用来自 1998 年至 2013 年期间美国 39 个癌症登记处的数据,为 0 至 19 岁的人群估计 DTC 的年龄标准化发病率(ASR)和原发性 DTC 发病率的年百分比变化(APC)。
1998 年至 2013 年间,诊断出 7296 例 DTC(6652 例乳头状病例和 644 例滤泡状病例)。小儿 DTC 的 APC 显著增加了 4.43%/y[95%CI,3.74%/y-5.13%/y],主要是由于乳头状组织学的增加。男女两性、非西班牙裔白种人、非西班牙裔黑人和西班牙裔儿童的 10 至 19 岁年龄组均观察到上升趋势。所有肿瘤分期(APC,+4.06%/y[95%CI,2.84%/y-5.29%/y];APC,+5.68%/y[95%CI,4.64%/y-6.73%/y];APC,+8.55%/y[95%CI,5.03%/y-12.19%/y])和肿瘤大小(APC,+9.46%/y[95%CI,6.13%/y-12.90%/y];APC,+6.92%/y[95%CI,4.31%/y-9.60%/y];APC,+4.69%/y[95%CI,2.75%/y-6.67%/y])的时间均呈显著上升趋势。
美国 10 至 19 岁儿童中 DTC 的发病率随时间推移呈显著上升趋势,这不太可能完全归因于儿童期医疗监测的增加,因为大型晚期 DTC 的发病率随时间推移而上升。未来的研究应检查可能导致 DTC 发病率上升的环境和其他因素。