Evidence map›Paper›PMID 40770073›Full record

ArticleLeukemia2025

Young unrelated donors confer a survival advantage for patients with myeloid malignancies compared to older siblings.

Johannes Schetelig, Henning Baldauf, Carina Rave, Gesine Bug, Lutz P Müller, Eva Maria Wagner-Drouet, Francis Ayuketang Ayuk, Wolfgang Bethge, Matthias Stelljes, Thomas Schroeder and 15 more

Abstract readComparative Study
In one paragraph

Article in Leukemia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Guideline
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  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

25 authors.

Johannes Schetelig *Department of Internal Medicine I, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany. johannes.schetelig@ukdd.de.ORCID 0000-0002-2780-2981
Henning Baldauf *DKMS Clinical Trials Unit, DKMS Group, Dresden, Germany.
Carina RaveDKMS Clinical Trials Unit, DKMS Group, Dresden, Germany.
Gesine BugGoethe University Frankfurt, University Hospital, Department of Medicine 2, Frankfurt, Germany.ORCID 0000-0003-2359-131X
Lutz P MüllerDepartment of Internal Medicine IV, University Hospital Halle, Halle, Germany.ORCID 0000-0002-2212-8166
Eva Maria Wagner-DrouetDepartment of Medicine III, University Medical Center, Johannes Gutenberg University Mainz, Mainz, Germany.ORCID 0000-0002-0728-2253
Francis Ayuketang AyukDepartment of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0001-6297-1847
Wolfgang BethgeDepartment of Hematology, Oncology, Clinical Immunology and Rheumatology; University Hospital Tübingen, Tübingen, Germany.ORCID 0000-0001-6052-2618
Matthias StelljesDepartment of Medicine A, Hematology, Oncology, and Pneumology, University Hospital Münster, Münster, Germany.ORCID 0000-0002-9331-5145
Thomas SchroederUniversity Hospital Essen, Department of Hematology and Stem Cell Transplantation, West German Cancer Center, Essen, Germany.
Friedrich StölzelDivision of Stem Cell Transplantation and Cellular Immunotherapy, University Hospital Schleswig-Holstein, Kiel, Germany.ORCID 0000-0003-0653-5332
Edgar JostDepartment of Hematology, Oncology, Hemostaseology and Stem Cell Transplantation, Medical Faculty, RWTH Aachen University & Center for Integrated Oncology Aachen Bonn Cologne Düsseldorf (CIO ABCD), Aachen, Germany.
Christoph SchmidDepartment of Hematology and Oncology, Augsburg University Hospital and Medical Faculty, Bavarian Cancer Research Center (BZKF) and Comprehensive Cancer Center Augsburg, Augsburg, Germany.ORCID 0000-0001-7070-487X
Desiree KunadtDepartment of Internal Medicine I, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.
Katja SockelDepartment of Internal Medicine I, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.ORCID 0000-0003-1732-7299
Katharina Egger-HeidrichDepartment of Internal Medicine I, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.
Jan Moritz MiddekeDepartment of Internal Medicine I, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.
Daniel FürstInstitute for Clinical Transfusion Medicine and Immunogenetics Ulm, German Red Cross Blood Transfusion Service, Baden Wuerttemberg - Hessen and University Hospital Ulm, Ulm, Germany.ORCID 0000-0001-9542-3169
Daniel SchefzykDKMS Clinical Trials Unit, DKMS Group, Dresden, Germany.
Jürgen SauterDKMS Clinical Trials Unit, DKMS Group, Dresden, Germany.ORCID 0000-0001-8485-2945
Alexander H SchmidtDKMS Clinical Trials Unit, DKMS Group, Dresden, Germany.
Katharina FleischhauerInstitute for Experimental Cellular Therapy, University Hospital Essen, Essen, Germany.
Martin BornhäuserDepartment of Internal Medicine I, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.ORCID 0000-0002-5916-3029
German Cooperative Transplant Study Group
Deutsches Register für hämatopoetische Stammzelltransplantation und Zelltherapie (DRST)

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Donor age is one factor to optimize allogeneic hematopoietic cell transplantation (alloHCT). Therefore, we investigated whether young unrelated donors (UD) provide a benefit for older patients with myeloid malignancies compared to HLA-identical sibling donors (MSD). We performed a retrospective registry study on patients ≥50 years who received a first alloHCT between 2010 and 2020. We compared event-free survival (EFS) of patients who were transplanted from MSD aged ≥50 years versus UD aged ≤35 years who were HLA-compatible for HLA-A, -B, -C, and -DRB1. In total, we analyzed data from 3460 patients. With multivariable adjustment EFS (HR 0.86, p = 0.003), OS (HR 0.82, p < 0.001), and risk of relapse (HR 0.84, p = 0.018) were significantly better for HLA-compatible UD compared to MSD. No survival advantage was found, when UD with unfavorable sex or CMV constellation were compared to MSD with favorable constellations. In a meta-analysis on 9905 patients with myeloid malignancies, including ours, we found reduced risk of relapse (pooled HR 0.78, p = 0.006) and better EFS (pooled HR 0.89, p < 0.001) for young matched UD versus MSD. To select young HLA-compatible UD over older MSD may reduce relapse risk and improve survival for older patients with myeloid malignancies.

Indexed as

Hematopoietic Stem Cell TransplantationSiblingsUnrelated DonorsAdultAgedAge FactorsFemaleFollow-Up StudiesGraft vs Host DiseaseHumansMaleMiddle AgedPrognosisRegistriesRetrospective StudiesSurvival Rate

Identifiers

PMID40770073
PMCPMC12463653

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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.