Evidence map›Paper›PMID 40067123›Full record

Observational studyBlood2025

Social determinants of health and access to allogeneic hematopoietic cell transplantation for acute myeloid leukemia.

Natalie Wuliji, Salene M W Jones, Ted Gooley, Aaron T Gerds, Bruno C Medeiros, Paul J Shami, John Galvin, Kehinde Adekola, Selina Luger, Maria R Baer and 15 more

Registry-linked trialAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Blood, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01929408 (Feasibility and Outcomes of Allogeneic Hematopoietic Cell Transplantation), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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.

NCT01929408 completednot on this map

Feasibility and Outcomes of Allogeneic Hematopoietic Cell Transplantation (HCT) Compared to Conventional Therapy for Older and Medically Infirm Patients Diagnosed With Acute Myeloid Leukemia or High-Risk Myelodysplastic Syndromes: A Prospective Observational Study

TypeobservationalSponsorFred Hutchinson Cancer CenterRan2013 to 2018Enrolled703ConditionsAcute Myeloid Leukemia (AML), Myelodysplastic Syndrome (MDS)
3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
  2. Refining favorable-risk classification in pediatricBlood science (Baltimore, Md.) · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors.

Natalie WulijiClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.
Salene M W JonesPublic Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0003-2140-5798
Ted GooleyClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.
Aaron T GerdsHematology and Medical Oncology, Cleveland Clinic, Cleveland, OH.ORCID 0000-0002-3422-1309
Bruno C MedeirosDivision of Hematology, Department of Medicine, Stanford University, Stanford, Palo Alto, CA.
Paul J ShamiDivision of Hematology and Hematologic Malignancies, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.
John GalvinUniversity of Illinois Chicago Cancer Center, Chicago, IL.
Kehinde AdekolaRobert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL.ORCID 0000-0001-7166-9308
Selina LugerAbramson Cancer Center, University of Pennsylvania, Philadelphia, PA.
Maria R BaerUniversity of Maryland Greenebaum Comprehensive Cancer Center, Baltimore, MD.
David RizzieriNovant Heath, Cancer Institute, Charlotte, NC.
Tanya M WildesDivision of Oncology and Hematology, University of Nebraska Medical Center, Omaha, NE.
Eunice S WangLeukemia Service, Roswell Park Comprehensive Cancer Center, Buffalo, NY.ORCID 0000-0002-8644-0968
Mikkael A SekeresUniversity of Miami, Sylvester Comprehensive Cancer Center, Miami, FL.ORCID 0000-0003-2009-6524
Sudipto MukherjeeHematology and Medical Oncology, Cleveland Clinic, Cleveland, OH.
Julie SmithConfluence Health/Wenatchee Valley Hospital and Clinic, Wenatchee, WA.
Mitchell GarrisonConfluence Health/Wenatchee Valley Hospital and Clinic, Wenatchee, WA.
Kiarash KojouriSkagit Valley Hospital, Mount Vernon, WA.
Jacob AppelbaumClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0002-4362-7773
Mary-Elizabeth PercivalClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.
Brenda M SandmaierDivision of Hematology and Oncology, University of Washington School of Medicine, Seattle, WA.ORCID 0000-0002-9767-9739
Stephanie LeeClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0003-2600-6390
Frederick R AppelbaumClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.
Rayne RouceSection of Hematology-Oncology, Department of Pediatrics, Baylor College of Medicine, Houston, TX.
Mohamed L SorrorClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

abstractWhether allogeneic hematopoietic cell transplant (allo-HCT) to treat acute myeloid leukemia (AML) is equitably accessible regardless of social determinants of health (SDOH) remains unknown. We examined associations of SDOH with access to allo-HCT and other outcomes. Patients presenting for treatment (n = 692) at 13 AML treatment centers were prospectively recruited to a registered clinical trial (number NCT01929408). Various patient-, AML-, and SDOH-specific variables were collected. Outcomes included mortality without allo-HCT, receipt of allo-HCT, and mortality after allo-HCT. Individual multivariable models (Fine-Gray for the first 2 outcomes, Cox regression for the third) were fit for each SDOH variable, adjusting for relevant patient- and AML-specific variables. Allo-HCT was used to treat 46% of patients. A 10% increase in the proportion with less than a high school education, in households receiving Supplemental Nutrition Assistance Program, receiving Supplemental Security Income, or in poverty led to modeled adjusted hazard ratios (aHRs) of 1.21 (0.99-1.46), 1.13 (0.97-1.31), 1.41 (1.01-1.97), and 1.16 (0.96-1.39) for death without allo-HCT. The aHRs were 0.67 (0.55-0.83), 0.88 (0.76-1.01), 0.71 (0.48-1.05), and 0.91 (0.75-1.09) for lessened receipt of allo-HCT. Among those who received allo-HCT, aHRs for mortality were 1.18 (0.87-1.60), 1.13 (0.92-1.38), 1.21 (0.81-1.82), and 1.04 (0.79-1.36). Results highlight increased mortality without allo-HCT and decreased access to allo-HCT, but lesser magnitude of increased mortality after allo-HCT, among patients from lower resourced areas due to limited education and/or increased poverty. Targeted interventions and policy changes are needed to ensure that marginalized patient populations have equitable chances for AML cure compared with others.

Indexed as

Health Services AccessibilityHematopoietic Stem Cell TransplantationLeukemia, Myeloid, AcuteSocial Determinants of HealthAdolescentAdultAgedFemaleHumansMaleMiddle AgedProspective StudiesTransplantation, HomologousYoung Adult

Identifiers

PMID40067123
PMCPMC13122322

What OpenQuestion holds

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Registered trials

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.