Graduate Group in Epidemiology, University of California, Davis, Davis, CA; Department of Public Health Sciences, University of California, Davis, Davis, CA.
Department of Pediatrics, University of California, Davis, Davis, CA.
J Pediatr. 2021 Jul;234:172-180.e3. doi: 10.1016/j.jpeds.2021.03.001. Epub 2021 Mar 6.
To assess leukemia risks among children with Down syndrome in a large, contemporary cohort.
Retrospective cohort study including 3 905 399 children born 1996-2016 in 7 US healthcare systems or Ontario, Canada, and followed from birth to cancer diagnosis, death, age 15 years, disenrollment, or December 30, 2016. Down syndrome was identified using International Classification of Diseases, Ninth and Tenth Revisions, diagnosis codes. Cancer diagnoses were identified through linkages to tumor registries. Incidence and hazard ratios (HRs) of leukemia were estimated for children with Down syndrome and other children adjusting for health system, child's age at diagnosis, birth year, and sex.
Leukemia was diagnosed in 124 of 4401 children with Down syndrome and 1941 of 3 900 998 other children. In children with Down syndrome, the cumulative incidence of acute myeloid leukemia (AML) was 1405/100 000 (95% CI 1076-1806) at age 4 years and unchanged at age 14 years. The cumulative incidence of acute lymphoid leukemia in children with Down syndrome was 1059/100 000 (95% CI 755-1451) at age 4 and 1714/100 000 (95% CI 1264-2276) at age 14 years. Children with Down syndrome had a greater risk of AML before age 5 years than other children (HR 399, 95% CI 281-566). Largest HRs were for megakaryoblastic leukemia before age 5 years (HR 1500, 95% CI 555-4070). Children with Down syndrome had a greater risk of acute lymphoid leukemia than other children regardless of age (<5 years: HR 28, 95% CI 20-40, ≥5 years HR 21, 95% CI 12-38).
Down syndrome remains a strong risk factor for childhood leukemia, and associations with AML are stronger than previously reported.
在一个大型当代队列中评估唐氏综合征患儿的白血病风险。
这是一项回顾性队列研究,纳入了 1996 年至 2016 年期间在美国 7 个医疗保健系统或加拿大安大略省出生的 3905399 名儿童,并从出生到癌症诊断、死亡、15 岁、退出或 2016 年 12 月 30 日进行随访。唐氏综合征通过国际疾病分类第 9 次和第 10 次修订版的诊断代码来识别。通过与肿瘤登记处的链接来确定癌症诊断。调整了医疗系统、患儿诊断时的年龄、出生年份和性别后,估计了唐氏综合征患儿和其他患儿的白血病发病率和危险比(HR)。
在 4401 名唐氏综合征患儿中有 124 例和 3900998 名其他患儿中有 1941 例诊断出白血病。在唐氏综合征患儿中,4 岁时急性髓系白血病(AML)的累积发病率为 1405/100000(95%CI 1076-1806),14 岁时未发生变化。唐氏综合征患儿急性淋巴细胞白血病的累积发病率为 4 岁时 1059/100000(95%CI 755-1451),14 岁时 1714/100000(95%CI 1264-2276)。5 岁以下儿童患 AML 的风险高于其他儿童(HR 399,95%CI 281-566)。5 岁前最大 HR 见于巨核细胞白血病(HR 1500,95%CI 555-4070)。无论年龄大小(<5 岁:HR 28,95%CI 20-40,≥5 岁 HR 21,95%CI 12-38),唐氏综合征患儿患急性淋巴细胞白血病的风险均高于其他儿童。
唐氏综合征仍然是儿童白血病的一个强烈危险因素,与 AML 的关联比以前报道的更强。