Evidence map›Paper›PMID 40845260›Full record

ArticleBlood advances2025

Neighborhood socioeconomic status and overall survival among children with acute lymphoblastic leukemia.

Anna L Hoppmann, Deborah M Hurley, Stuart Cramer, Monique J Brown, Rahul Ghosal, Anthony J Alberg, Smita Bhatia

Abstract read
In one paragraph

Article in Blood advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Anna L HoppmannDepartment of Pediatrics, University of South Carolina School of Medicine, Columbia, SC.ORCID 0009-0007-6996-6056
Deborah M HurleyPrisma Health, Columbia, SC.ORCID 0000-0001-5109-0227
Stuart CramerDepartment of Pediatrics, University of South Carolina School of Medicine, Columbia, SC.
Monique J BrownDepartment of Epidemiology and Biostatistics, Arnold School of Public Health, University of South Carolina, Columbia, SC.ORCID 0000-0001-9552-244X
Rahul GhosalDepartment of Epidemiology and Biostatistics, Arnold School of Public Health, University of South Carolina, Columbia, SC.
Anthony J AlbergDepartment of Epidemiology and Biostatistics, Arnold School of Public Health, University of South Carolina, Columbia, SC.
Smita BhatiaHeersink School of Medicine, Institute for Cancer Outcomes and Survivorship, The University of Alabama at Birmingham, Birmingham, AL.ORCID 0000-0002-7755-5683

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractA disadvantaged neighborhood, as represented by area-level socioeconomic status (SES), has been associated with adverse outcomes among children with acute lymphoblastic leukemia (ALL) in the United States, but the duration of impact after ALL diagnosis is not well understood. This retrospective cohort study used the National Cancer Database to evaluate the impact of area-level SES on overall survival among children with ALL. Median income and education quartiles based on residential zip code were used to create a composite area-level SES variable. Individual-level variables included age, sex, race, year of diagnosis, primary payer, distance to care, rurality, time to treatment, and comorbidity index. Cox proportional hazard models were created overall and conditional on surviving 2 and 5 years from diagnosis. This cohort of 17 044 children with ALL consisted of 57% males, 61% non-Hispanic White, 24% Hispanic, 8% non-Hispanic Black, 5% Asian, and 2% other race/ethnicities. Furthermore, 12% (1971) resided in the lowest SES neighborhoods, whereas 18% resided in the highest SES neighborhoods. Compared with those in the highest SES neighborhoods, children in the lowest SES neighborhoods had a 55% increased hazard of all-cause mortality (95% confidence interval [CI], 1.29-1.88; P < .001). The increased hazard of mortality among those from the lowest SES neighborhoods persisted among those who survived 2 years (hazard ratio [HR], 1.70; 95% CI, 1.28-2.26; P = .001) and 5 years (HR, 1.87; 95% CI, 1.17-3.00; P = .032) after ALL diagnosis. These findings suggest the need for long-term strategies to support at-risk patients beyond completion of frontline therapy.

Indexed as

Neighborhood CharacteristicsPrecursor Cell Lymphoblastic Leukemia-LymphomaResidence CharacteristicsSocial ClassAdolescentChildChild, PreschoolFemaleHumansInfantMaleProportional Hazards ModelsRetrospective StudiesUnited States

Identifiers

PMID40845260
PMCPMC12663511

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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.