Evidence map›Paper›PMID 39888631›Full record

ArticleBlood advances2025

Evolving racial/ethnic disparities in AML survival in the novel therapy era.

Xin Wang, Phyllis A Gimotty, Andrew H Matthews, Ronac Mamtani, Selina M Luger, Elizabeth O Hexner, Daria V Babushok, Shannon R McCurdy, Noelle V Frey, Ximena Jordan Bruno and 10 more

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. 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.

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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Observational
  4. The global epidemiology of acute myeloid leukaemia.Nature reviews. Clinical oncology · 2026
    Review
  5. Review
  6. Article
  7. Article
  8. Review
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

20 authors.

Xin WangDivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.ORCID 0000-0001-9827-3098
Phyllis A GimottyDepartment of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.ORCID 0000-0002-3850-9799
Andrew H MatthewsDivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.ORCID 0000-0002-4904-3998
Ronac MamtaniDivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
Selina M LugerDivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
Elizabeth O HexnerDivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.ORCID 0000-0002-1125-4060
Daria V BabushokDivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
Shannon R McCurdyDivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
Noelle V FreyDivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.ORCID 0000-0003-3688-9836
Ximena Jordan BrunoDivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
Saar GillDivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
Mary Ellen MartinDivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
Vikram R ParalkarDivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.ORCID 0000-0001-6413-951X
Ivan MaillardDivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.ORCID 0000-0003-1312-6748
David L PorterDivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
Alison W LorenDivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
Alexander E PerlDivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.ORCID 0000-0002-1463-2231
Keith W PratzDivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
Kelly D GetzDepartment of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Catherine LaiDivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.ORCID 0000-0001-8861-0281

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Racial/ethnic disparities in acute myeloid leukemia survival in the novel therapy era: an exploration of the underlying mechanisms and potential targets for interventionF32MD018944 · NIMHD · UNIVERSITY OF PENNSYLVANIA · PI WANG, XIN · 2023 to 2023
$97k
NCI NIH HHS P30 CA008748NIMHD NIH HHS F32 MD018944
6 · The paper itself

Abstract

abstractLittle is known about the impact of recent advances in acute myeloid leukemia (AML) treatment on racial/ethnic disparities in survival outcomes. We performed a retrospective cohort study of patients with newly diagnosed AML using data from a nationwide electronic health record-derived deidentified database. Patients were categorized based on their diagnosis date relative to venetoclax approval, as pre-novel therapy era (Pre era; 2014-2018; n = 2998) or post-novel therapy era (Post era; 2019-2022; n = 2098). Patients in the Post era were older and had more comorbidities than Pre era. Non-Hispanic Black (NHB) and Hispanic patients were younger and more likely to have lower socioeconomic status than non-Hispanic White (NHW) patients, with no differences in the distributions of key disease features. After accounting for age and comorbidity, overall survival (OS) was higher in patients in Post era than Pre era (adjusted hazard ratio [aHR], 0.90; 95% confidence interval [CI], 0.83-0.96). In Pre era, NHB had a 22% higher hazard of death than NHW (aHR, 1.22; 95% CI, 1.04-1.43), whereas worse OS was not observed for NHB in Post era (aHR, 0.86; 95% CI, 0.69-1.08; predicted 2-year survival, 45.3% vs 39.9%). Utilization of novel therapeutics in frontline therapy did not differ by race/ethnicity. Among patients receiving venetoclax-based induction, particularly those without TP53, RAS, or FLT3-ITD mutations, results suggested higher OS for NHB than NHW patients (aHR, 0.67; 95% CI, 0.45-1.01). Additional studies are needed to elucidate factors contributing to these observed survival differences and to inform strategies to optimize outcomes for all patients with AML.

Indexed as

Healthcare DisparitiesLeukemia, Myeloid, AcuteAdultAgedAged, 80 and overBlack or African AmericanBridged Bicyclo Compounds, HeterocyclicFemaleHispanic or LatinoHumansMaleMiddle AgedRetrospective StudiesSulfonamidesWhiteBridged Bicyclo Compounds, HeterocyclicSulfonamidesvenetoclax

Identifiers

PMID39888631
PMCPMC11821405

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.