Evidence map›Paper›PMID 42584892›Full record

ArticleJAMA network open2026

Race and Ethnicity and Overall Survival in Pediatric Acute Myeloid Leukemia.

Daniel J Zheng, Long Khuong, Catherine Aftandilian, Kira Bona, Emi H Caywood, Caitlin W Elgarten, Brian T Fisher, Cody-Aaron L Gathers, Taumoha Ghosh, M Monica Gramatges and 20 more

Abstract read
In one paragraph

Article in JAMA network open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

30 authors.

Daniel J ZhengDepartment of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia.
Long KhuongDepartment of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia.
Catherine AftandilianDepartment of Pediatrics, Division of Pediatric Hematology, Oncology, Stem Cell Transplantation and Regenerative Medicine, Stanford University, Palo Alto, California.
Kira BonaDana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, Massachusetts.
Emi H CaywoodDepartment of Pediatrics, Thomas Jefferson University, Philadelphia, Pennsylvania.
Caitlin W ElgartenPerelman School of Medicine, University of Pennsylvania, Philadelphia.
Brian T FisherDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Cody-Aaron L GathersDivision of Cardiology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Taumoha GhoshDepartment of Pediatrics, Division of Pediatric Hematology and Oncology, Primary Children's Hospital and University of Utah, Salt Lake City.
M Monica GramatgesTexas Children's Hospital, Baylor College of Medicine, Houston, Texas.
Gary HettingerDepartment of Population Health, New York University Grossman School of Medicine, New York.
Meret R HenryDepartment of Pediatrics, Division of Pediatric Hematology-Oncology and Pediatric Bone Marrow Transplant, Children's Hospital of Michigan, Detroit.
Yuan-Shung V HuangDepartment of Biomedical and Health Informatics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Yimei LiDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Kelly MaloneyChildren's Hospital Colorado, Aurora.
Amir MianDivision of Pediatric Hematology/Oncology, Dell Children's Medical Center, The University of Texas at Austin.
Tamara P MillerAflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Atlanta, Georgia.
Arunkumar ModiHematology and Oncology, AdventHealth Medical Group Stem Cell Transplant and Cellular Therapy at Orlando, Orlando, Florida.
Rajen ModyDepartment of Pediatrics University of Michigan, Ann Arbor.
Regina M MyersDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Haley NewmanDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Jose OrtizDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Alix E SeifDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Caroline SmithDepartment of Pediatrics, The University of Texas Southwestern Medical Center, Dallas.
Jamie StokkeChildren's Hospital of Los Angeles, Los Angeles, California.
Naomi WinickDepartment of Pediatrics, The University of Texas Southwestern Medical Center, Dallas.
Jennifer J WilkesDepartment of Pediatrics, University of Washington School of Medicine, Seattle.
Victor WongDivision of Pediatric Hematology Oncology, Rady Children's Hospital San Diego, San Diego, California.
Richard AplencDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Kelly D GetzDepartment of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Hispanic and non-Hispanic Black (hereafter, Black) children with acute myeloid leukemia (AML) have historically experienced worse survival outcomes compared with non-Hispanic White (hereafter, White) children. Understanding specific intermediate pathways underlying these outcome disparities is a critical step to directing interventional efforts and resources. Objective: To compare survival outcomes by race and ethnicity in a large contemporary cohort of pediatric patients with AML and to examine presentation acuity, frontline organ toxic effects, and relapse as potential mediators of any observed outcome disparities. Design, Setting, and Participants: This retrospective cohort study was analyzed from April 2025 to January 2026 and included 13 US children's hospitals across 10 states participating in the Real-World Epidemiology of Acute Leukemia-AML cohort. Participants included children treated for de novo AML from January 2011 through May 2024. Exposure: Race and ethnicity (Black, Hispanic, and White). Main Outcomes and Measures: The main outcome was overall survival (OS), defined as the time from AML diagnosis until death from any cause. Results: The study cohort included 773 children (median [IQR] age, 9 [2-14] years; 402 males [52.0%]), of whom 125 (16.2%) were Black, 237 (30.7%) were Hispanic, and 411 (53.2%) were White (median [IQR] follow-up, 51.2 [25.7-86.9] months), treated for de novo AML. Among the patients, Black (5-year OS, 61.1% [95% CI, 52.6%-71.0%]; adjusted hazard ratio [AHR], 1.55 [95% CI, 1.26-1.91]) and Hispanic (5-year OS, 65.4% [95% CI, 58.9%-72.5%]; AHR, 1.32 [95% CI, 1.03-1.68]) children had worse OS compared with White children (5-year OS, 70.0% [95% CI, 65.2%-75.1%]). Compared with White patients, Black patients had increased risk of higher cardiovascular (adjusted risk ratio [ARR], 2.09 [95% CI, 1.23-3.56]), respiratory (ARR, 1.36 [95% CI, 1.05-1.77]), and renal (ARR, 3.08 [95% CI, 1.02-9.32]) acuity at presentation. There were no statistically significant increases in severe frontline organ toxic effects or relapse rates by race and ethnicity. Cardiovascular acuity (AHR, 1.83 [95% CI, 1.51-2.22]) and respiratory acuity (AHR, 1.43 [95% CI, 1.15-1.77]) at presentation were independently associated with all-cause mortality. Cardiovascular acuity (proportion mediated, 14%) and respiratory acuity (proportion mediated, 8%) at presentation partially mediated the total absolute survival difference between Black and White children. Conclusions and Relevance: In this cohort study of pediatric patients with AML, differential cardiovascular and respiratory acuity at presentation were partial mediators of outcome disparities for Black children with AML. Other intermediates along the care continuum should be identified to account for the remainder of the observed outcomes and to prioritize focus areas for interventional efforts to mitigate the survival differences.

Indexed as

Leukemia, Myeloid, AcuteAdolescentBlack or African AmericanChildChild, PreschoolFemaleHispanic or LatinoHumansMaleRetrospective StudiesUnited StatesWhite

Identifiers

PMID42584892
PMCPMC13470291

What OpenQuestion holds

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Registered trials

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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.