Evidence map›Paper›PMID 42839030›Full record

ArticleBone marrow transplantation2026

GvHD prophylaxis in elderly patients: post-transplant cyclophosphamide or ATG? A study by the EBMT transplant complications working party.

Lars Klingen Gjærde, Christophe Peczynski, William Boreland, Henrik Sengeløv, Didier Blaise, Tobias Gedde-Dahl, Igor Wolfgang Blau, Jonathan Bordat, Thomas Schroeder, Nicolaus Kröger and 11 more

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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

21 authors.

Lars Klingen GjærdeDepartment of Hematology, Rigshospitalet, Copenhagen, Denmark. lars.klingen.gjaerde@regionh.dk.ORCID http://orcid.org/0000-0002-5496-9955
Christophe PeczynskiEBMT Paris Study Unit, Department of Haematology, Saint Antoine Hospital, INSERM UMR 938, Sorbonne University, Paris, France.
William BorelandEBMT Paris Study Unit, Department of Haematology, Saint Antoine Hospital, INSERM UMR 938, Sorbonne University, Paris, France.ORCID http://orcid.org/0009-0007-9739-0816
Henrik SengeløvDepartment of Hematology, Rigshospitalet, Copenhagen, Denmark.
Didier BlaiseDepartement D'Hematologie, Programme de Transplantation et de Therapie Cellulaire, Centre de Recherche en Cancerologie de Marseille, Institut Paoli Calmettes, Marseille, France.ORCID http://orcid.org/0000-0002-5684-9447
Tobias Gedde-DahlDepartment of Hematology, Institute of Clinical Medicine, University of Oslo and Oslo University Hospital-Rikshospitalet, Oslo, Norway.
Igor Wolfgang BlauDepartment of Hematology, Oncology and Tumor Immunology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Jonathan BordatBone Marrow Transplantation Unit, Saint Louis Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.
Thomas SchroederDepartment of Hematology, Oncology, and Clinical Immunology, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.
Nicolaus KrögerDepartment of Stem Cell Transplantation, University Medical Center Hamburg, Hamburg, Germany.ORCID http://orcid.org/0000-0001-5103-9966
Francesca KinsellaBirmingham Centre for Cellular Therapy and Transplantation, University Hospitals Birmingham, Birmingham, UK.
Stephan MielkeDepartment of Allogeneic Stem Cell Transplantation and Cell Therapy (CAST), Department of Laboratory Medicine and Department of Medicine Huddinge, Karolinska Comprehensive Cancer Center, Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden.
Matthias EderDepartment of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.ORCID http://orcid.org/0009-0000-3362-5814
Fabio CiceriVita-Salute San Raffaele University, Milano, Italy; Division of Immunology, Transplantation and Infectious Diseases, IRCCS San Raffaele Scientific Institute, Milan, Italy.ORCID http://orcid.org/0000-0003-0873-0123
Donal P McLornanDepartment of Haematology and Stem Cell Transplantation, University College London, London, UK.ORCID http://orcid.org/0000-0003-1224-091X
Helene SchoemansDepartment of Hematology, University Hospitals Leuven, Leuven, Belgium & Department of Public Health and Primary Care, ACCENT VV, KU Leuven - University of Leuven, Leuven, Belgium.ORCID http://orcid.org/0000-0002-7568-8239
Charlotte GrahamComprehensive Cancer Centre, King's College London, London, UK.ORCID http://orcid.org/0000-0001-7874-7305
Alberto MussettiDepartment of Hematology, Hospital Duran i Reynals, Instituto Catalán de Oncología, L'Hospitalet De Llobregat, Barcelona, Spain.ORCID http://orcid.org/0000-0002-4088-036X
Zinaida PericDepartment of Hematology, University Hospital Centre Rijeka, Rijeka, Croatia.
Ivan MoiseevRM Gorbacheva Research Institute, Pavlov University, St Petersburg, Russian Federation.ORCID http://orcid.org/0000-0002-4332-0114
Olaf PenackDepartment of Hematology, Oncology and Tumor Immunology, Charité - Universitätsmedizin Berlin, Berlin, Germany.ORCID http://orcid.org/0000-0003-4876-802X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allogeneic hematopoietic cell transplantation (allo‑HCT) has become increasingly feasible in older patients with hematologic malignancies, yet the optimal graft‑versus‑host disease (GvHD) prophylaxis in this population remains uncertain. We compared post‑transplant cyclophosphamide (PTCy) with anti‑thymocyte globulin (ATG) in patients aged ≥60 years undergoing reduced‑intensity conditioning (RIC) peripheral blood stem cell allo‑HCT, using EBMT registry data from 2016 to 2022. A total of 7507 patients were included: 1418 matched sibling donors (MSD), 5051 matched unrelated donors (MUD), and 1038 mismatched unrelated donor (MMUD) transplants. In MSD recipients aged >65 years, PTCy was associated with reduced relapse, improved progression‑free survival (PFS), and superior GvHD‑ and relapse‑free survival (GRFS). However, in MSD recipients aged 60-65 years, these outcomes did not differ significantly between PTCy and ATG. Among MUD recipients, PTCy was associated with lower relapse and chronic GvHD, and a higher PFS, GRFS, and overall survival. In MMUD transplants, outcomes were not significantly different. Our findings indicate that PTCy is a safe and effective alternative to ATG in older allo‑HCT recipients, especially in MUD transplants and in MSD recipients aged >65 years, but the findings should be interpreted cautiously given their observational nature and patient heterogeneity. Further studies are warranted to assess long‑term outcomes.

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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.