Evidence map›Paper›PMID 33684394›Full record

ArticleThe Journal of pediatrics2021

Leukemia Risk in a Cohort of 3.9 Million Children with and without Down Syndrome.

Emily C Marlow, Jonathan Ducore, Marilyn L Kwan, Stephanie Y Cheng, Erin J A Bowles, Robert T Greenlee, Jason D Pole, Alanna Kulchak Rahm, Natasha K Stout, Sheila Weinmann and 2 more

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in The Journal of pediatrics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
7.7field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 55 citations in OpenAlex.

  1. Pooled it
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  11. Spatial distribution of acute myeloid leukaemia in Denmark.Environmental health : a global access science source · 2025
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  18. Too many white cells-TAM, JMML, or something else?Hematology. American Society of Hematology. Education Program · 2023
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 8 institutions in 3 countries.

Emily C MarlowGraduate Group in Epidemiology, University of California, Davis, Davis, CA; Department of Public Health Sciences, University of California, Davis, Davis, CA.
Jonathan DucoreDepartment of Pediatrics, University of California, Davis, Davis, CA.
Marilyn L KwanDivision of Research, Kaiser Permanente Northern California, Oakland, CA.
Stephanie Y ChengICES, Toronto, Ontario, Canada.
Erin J A BowlesKaiser Permanente Washington Health Research Institute, Kaiser Permanente Washington, Salt Lake City, UT.
Robert T GreenleeMarshfield Clinic Research Institute, Marshfield Clinic Health System, Marshfield, WI.
Jason D PoleICES, Toronto, Ontario, Canada; Centre for Health Service Research, University of Queensland, Brisbane, Australia; Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
Alanna Kulchak RahmGenomic Medicine Institute, Geisinger, Forty Fort, PA.
Natasha K StoutDepartment of Population Medicine, Harvard Medical School and Harvard Pilgrim Health Care Institute, Boston, MA.
Sheila WeinmannCenter for Health Research, Kaiser Permanente Northwest, Portland, OR; Center for Integrated Health Care Research, Kaiser Permanente Hawaii, Honolulu, HI.
Rebecca Smith-BindmanDepartment of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA; Department of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, CA; Department of Obstetrics, Gynecology and Reproductive Medicine, University of California, San Francisco, San Francisco, CA; Philip R. Lee Institute for Health Policy Studies, University of California, San Francisco, San Francisco, CA.
Diana L MigliorettiDepartment of Public Health Sciences, University of California, Davis, Davis, CA; Kaiser Permanente Washington Health Research Institute, Kaiser Permanente Washington, Salt Lake City, UT. Electronic address: dmiglioretti@ucdavis.edu.
Kaiser Permanente · USUniversity of California, Davis · USHarvard University · USInstitute for Clinical Evaluative Sciences · CAKaiser Permanente Washington Health Research Institute · USLee University · USMarshfield Clinic · USThe University of Queensland · AU

Funding

Risk of Pediatric and Adolescent Cancer Associated with Medical ImagingR01CA185687 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KWAN, MARILYN L, MIGLIORETTI, DIANA L · 2015 to 2019
$10.0M
Group Health Cancer Research Program Research Specialist AwardR50CA211115 · NCI · KAISER FOUNDATION RESEARCH INSTITUTE · PI BOWLES, ERIN JANELLE AIELLO · 2017 to 2021
$919k
NCI NIH HHS R01 CA185687NCI NIH HHS R50 CA211115
6 · The paper itself

Abstract

objectiveTo assess leukemia risks among children with Down syndrome in a large, contemporary cohort. STUDY

designRetrospective 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.

resultsLeukemia 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).

conclusionsDown syndrome remains a strong risk factor for childhood leukemia, and associations with AML are stronger than previously reported.

Indexed as

AdolescentCase-Control StudiesChildChild, PreschoolCohort StudiesDown SyndromeFemaleHumansIncidenceInfantInfant, NewbornLeukemia, Megakaryoblastic, AcuteMaleOntarioRegistriesRisk Assessmentacute lymphoid leukemiaacute myeloid leukemiachildhood leukemia riskDown syndromeretrospective cohort

Identifiers

PMID33684394
PMCPMC8238875
OpenAlexW3135628855

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.