Evidence map›Paper›PMID 41951842›Full record

ArticleBone marrow transplantation2026

Haploidentical transplantation with post-transplant cyclophosphamide is not inferior to 9/10-MUD transplantation with ATG in patients with myeloid malignancies.

Andrea Gantner, Svenja Labuhn, Daniel Fürst, Sophie Mannes, Sarah Flossdorf, Francis Ayuketang Ayuk, Thomas Schroeder, Matthias Stelljes, Robert Zeiser, Peter Dreger and 14 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Bone marrow transplantation, 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

24 authors.

Andrea GantnerDepartment of Internal Medicine III, University Hospital of Ulm, Ulm, Germany.
Svenja LabuhnInstitute of Statistics, University of Ulm, Ulm, Germany.
Daniel FürstDepartment of Transplantation Immunology, Institute of Clinical Transfusion Medicine and Immunogenetics Ulm, Ulm, Germany.ORCID http://orcid.org/0000-0001-9542-3169
Sophie MannesGerman Registry for Hematopoietic Stem Cell Transplantation and Cell Therapy (DRST), Frankfurt, Germany.
Sarah FlossdorfGerman Registry for Hematopoietic Stem Cell Transplantation and Cell Therapy (DRST), Frankfurt, Germany.ORCID http://orcid.org/0000-0003-0642-7104
Francis Ayuketang AyukDepartment of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID http://orcid.org/0000-0001-6297-1847
Thomas SchroederDepartment of Hematology and Stem Cell Transplantation, West German Cancer Center Essen, University Hospital Essen, Essen, Germany.
Matthias StelljesDepartment of Medicine A/Hematology and Oncology, University Hospital Münster, Münster, Germany.ORCID http://orcid.org/0000-0002-9331-5145
Robert ZeiserDepartment of Medicine I/Hematology and Oncology, Faculty of Medicine, Freiburg University Medical Center, Freiburg, Germany.ORCID http://orcid.org/0000-0001-6565-3393
Peter DregerDepartment of Hematology and Oncology, University Hospital Heidelberg, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-7429-8570
Matthias EderDepartment of Hematology, Hemostasis, Oncology, and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.ORCID http://orcid.org/0009-0000-3362-5814
Igor Wolfgang BlauMedical Clinic, Charité University Medicine Berlin, Berlin, Germany.
Johannes ScheteligMedizinische Klinik und Poliklinik I, Universitätsklinikum Carl Gustav Carus, Dresden, Germany.ORCID http://orcid.org/0000-0002-2780-2981
Arne BrechtDKD HELIOS Hospital Wiesbaden and HELIOS Dr. Horst Schmidt Hospitals Wiesbaden, Wiesbaden, Germany.
Andreas BurchertDepartment of Hematology, Oncology, and Immunology, Carreras Leukemia Center, Philips University Marburg and University Hospital Gießen and Marburg, Marburg, Germany.ORCID http://orcid.org/0000-0002-8411-8844
Matthias EdingerDepartment of Internal Medicine III, University Clinic Regensburg, Regensburg, Germany.
Verena WaisDepartment of Internal Medicine III, University Hospital of Ulm, Ulm, Germany.
Hubert SchrezenmeierDepartment of Transplantation Immunology, Institute of Clinical Transfusion Medicine and Immunogenetics Ulm, Ulm, Germany.
Hartmut DöhnerDepartment of Internal Medicine III, University Hospital of Ulm, Ulm, Germany.
Sandra SchmellerInstitute of Statistics, University of Ulm, Ulm, Germany.
Katharina FleischhauerGerman Registry for Hematopoietic Stem Cell Transplantation and Cell Therapy (DRST), Frankfurt, Germany.ORCID http://orcid.org/0000-0002-5827-8000
Nicolaus KrögerGerman Registry for Hematopoietic Stem Cell Transplantation and Cell Therapy (DRST), Frankfurt, Germany.
Elisa SalaDepartment of Internal Medicine III, University Hospital of Ulm, Ulm, Germany. elisa.sala@uniklinik-ulm.de.ORCID http://orcid.org/0009-0007-8090-0349
German Registry for Hematopoietic Stem Cell Transplantation and cell Therapy, DRST

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The selection of the best available donor is crucial for patients' outcome after allogeneic stem cell transplantation (allo-SCT). In the absence of fully Human leucocyte antigen (HLA) -matched donors, mismatched unrelated donor (9/10-MUD) or haploidentical donor (haplo) can be considered. No consensus has been reached on the best alternative and large real-world data are warranted to support decisional processes. We compared the outcome of 1413 patients with myeloid malignancies undergoing allo-SCT from 9/10-MUD with anti-thymocyte-globulin (ATG) (n = 1134) or haplo with post-transplant cyclophosphamide (PT-Cy, n = 279) between 2009 and 2020 in 48 German centres. Donor type with related graft versus host disease (GvHD) prophylaxis showed in multivariable analysis no significant impact on acute GvHD development, both grade II-IV (HR 0.90, 95% CI 0.69-1.19, p = 0.469) and severe (HR 1.22, 95% CI 0.82-1.81, p = 0.319), nor on moderate to severe chronic GvHD (HR 0.78, 95% CI 0.59-1.03, p = 0.077). Moreover, no influence from donor type was observed on GVHD-relapse-free survival (HR 1.12, 95% CI 0.92-1.36, p = 0.227), progression-free survival (HR 1.2, 95% CI 0.95-1.51, p = 0.121), non-relapse mortality (HR 1.1, 95% CI 0.81-1.51, p = 0.542) and overall survival (HR 1.16, 95% CI 0.91-1.48, p = 0.235). Our real-world data demonstrate that haplo allo-SCT with PT-Cy is not inferior to 9/10-MUD allo-SCT with ATG.

Indexed as

Antilymphocyte SerumCyclophosphamideHematopoietic Stem Cell TransplantationTransplantation ConditioningTransplantation, HaploidenticalAdolescentAdultAgedFemaleGraft vs Host DiseaseHumansMaleMiddle AgedUnrelated DonorsAntilymphocyte SerumCyclophosphamide

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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.