Evidence map›Paper›PMID 37898151›Full record

ReviewThe Lancet. Haematology2023

Germline predisposition traits in allogeneic hematopoietic stem-cell transplantation for myelodysplastic syndromes: a survey-based study and position paper on behalf of the Chronic Malignancies Working Party of the EBMT.

Carmelo Gurnari, Marie Robin, Lucy A Godley, Joanna Drozd-Sokołowska, Marcin W Włodarski, Kavita Raj, Francesco Onida, Nina Worel, Fabio Ciceri, Selim Carbacioglu and 22 more

Abstract readReviewConsensus Statement
In one paragraph

Review in The Lancet. Haematology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
6.7field-weighted citation impact, top 3% of its field
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

26 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  13. Myeloid neoplasms risks for germline DDX41 pathogenic variants carriers.European journal of human genetics : EJHG · 2025
    Article
  14. Genetic Predisposition to Hematologic Malignancies.Cold Spring Harbor perspectives in medicine · 2025
    Review
  15. Review
  16. Validation of Guidelines for Genetic Investigation of Myeloid Neoplasms with Germline Predisposition: Results from a Prospective Cohort Study.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  17. Review
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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

32 authors at 20 institutions in 13 countries.

Carmelo GurnariDepartment of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy; Department of Translational Hematology and Oncology Research, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH, USA.
Marie RobinDepartment of Hematology and Bone Marrow Transplantation, Hôpital Saint-Louis, AP-HP, University Paris, Paris, France.
Lucy A GodleySection of Hematology and Oncology, Departments of Medicine and Human Genetics, The University of Chicago, Chicago, IL, USA.
Joanna Drozd-SokołowskaDepartment of Hematology, Transplantation and Internal Medicine, Medical University of Warsaw, Warsaw, Poland.
Marcin W WłodarskiDepartment of Hematology, St Jude Children's Research Hospital, Memphis, TN, USA.
Kavita RajUniversity College London NHS Foundation Trust, London, UK.
Francesco OnidaHematology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Nina WorelDepartment of Transfusion Medicine and Cell Therapy, Medical University of Vienna, Vienna, Austria.
Fabio CiceriIRCCS Ospedale San Raffaele, Milano, Italy.
Selim CarbaciogluDepartment of Paediatric Oncology, Haematology and Stem Cell Transplantation, University Children's Hospital Regensburg, Regensburg, Germany.
Michelle KenyonDepartment of Haematological Medicine, King's College Hospital NHS Foundation Trust, London, UK.
Mahmoud AljurfDivision of Hematology, Stem Cell Transplantation and Cellular Therapy, Oncology Center, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Carmem BonfimPediatric Blood and Marrow Transplantation Division and Pele Pequeno Principe Research Institute, Hospital Pequeno Principe, Curitiba, Brazil.
Hideki MakishimaDepartment of Pathology and Tumor Biology, Kyoto University, Kyoto, Japan.
Charlotte NiemeyerDepartment of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Pierre FenauxDepartment of Hematology and Bone Marrow Transplantation, Hôpital Saint-Louis, AP-HP, University Paris, Paris, France; INSERM U944, CNRS UMR7212, Paris, France; Saint-Louis Hospital, Hematology Laboratory, AP-HP, Paris, France.
Armin ZebischDivision of Hematology and Otto Loewi Research Center for Vascular Biology, Immunology and Inflammation, Division of Pharmacology, Medical University of Graz, Graz, Austria.
Nada HamadDepartment of Hematology, St Vincent's Hospital Sydney, NSW, Australia.
Yves ChalandonDivision of Hematology, Bone Marrow Transplant Unit, University Hospital of Geneva and Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Eva Hellström-LindbergCenter for Hematology and Regenerative Medicine, Department of Medicine Huddinge, Karolinska Institutet and Department of Hematology, Karolinska University Hospital, Stockholm, Sweden.
Maria Teresa VosoDepartment of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy.
Cristina MecucciInstitute of Hematology and Center for Hemato-Oncology Research, University and Hospital of Perugia, Perugia, Italy.
Fernando Barroso DuarteFederal University of Ceará, Fortaleza, Brazil.
Marie SebertDepartment of Hematology and Bone Marrow Transplantation, Hôpital Saint-Louis, AP-HP, University Paris, Paris, France; INSERM U944, CNRS UMR7212, Paris, France; Saint-Louis Hospital, Hematology Laboratory, AP-HP, Paris, France.
Flore Sicre de FontbruneDepartment of Hematology and Bone Marrow Transplantation, Hôpital Saint Louis, AP-HP, Université Paris Cité, Centre National de Reference des Aplasies Médullaires Acquises et Constitutionnelles, Paris, France.
Jean SoulierINSERM U944, CNRS UMR7212, Paris, France; Saint-Louis Hospital, Hematology Laboratory, AP-HP, Paris, France.
Akiko ShimamuraDana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, MA, USA.
R Coleman LindsleyDana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Jarosław P MaciejewskiDepartment of Translational Hematology and Oncology Research, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH, USA.
Rodrigo T CaladoDepartment of Medical Imaging, Hematology, and Oncology, Ribeirão Preto Medical School, University of São Paulo, Brazil.
Ibrahim Yakoub-AghaCHU de Lille, University of Lille, INSERM U1286, Lille, France.
Donal P McLornanUniversity College London NHS Foundation Trust, London, UK. Electronic address: donal.mclornan@nhs.net.
Centre National de la Recherche Scientifique · FRUniversity College London Hospitals NHS Foundation Trust · GBUniversity of Rome Tor Vergata · ITAssistance Publique – Hôpitaux de Paris · FRCleveland Clinic · USDana-Farber/Boston Children's Cancer and Blood Disorders Center · USFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITHarvard University · USInserm · FRIRCCS Ospedale San Raffaele · ITKarolinska University Hospital · SEKing Faisal Specialist Hospital & Research Centre · SAKing's College Hospital NHS Foundation Trust · GBKyoto University · JPMedical University of Graz · ATMedical University of Vienna · ATMedical University of Warsaw · PLSt. Jude Children's Research Hospital · USSt Vincent's Hospital Sydney · AUUniversidade de São Paulo · BR

Funding

Systems Biology of Bone Marrow Failure and MDS for Precision MedicineRC2DK122533 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI FIGUEROA, MARIA EUGENIA, FLEMING, MARK D · 2019 to 2023
$6.4M
NIDDK NIH HHS RC2 DK122533
6 · The paper itself

Abstract

The recent application of whole exome or whole genome sequencing unveiled a plethora of germline variants predisposing to myeloid disorders, particularly myelodysplastic neoplasms. The presence of such variants in patients with myelodysplastic syndromes has important clinical repercussions for haematopoietic stem-cell transplantation, from donor selection and conditioning regimen to graft-versus-host disease prophylaxis and genetic counselling for relatives. No international guidelines exist to harmonise management approaches to this particular clinical scenario. Moreover, the application of germline testing, and how this informs clinical decisions, differs according to the expertise of individual clinical practices and according to different countries, health-care systems, and legislations. Leveraging the global span of the European Society for Blood and Marrow Transplantation (EBMT) network, we took a snapshot of the current European situation on these matters by disseminating an electronic survey to EBMT centres experienced in myelodysplastic syndromes transplantation. An international group of haematologists, transplantation physicians, paediatricians, nurses, and experts in molecular biology and constitutional genetics with experience in myelodysplastic syndromes contributed to this Position Paper. The panel met during multiple online meetings to discuss the results of the EBMT survey and to establish suggested harmonised guidelines for such clinical situations, which are presented here.

Indexed as

Graft vs Host DiseaseHematopoietic Stem Cell TransplantationMyelodysplastic SyndromesNeoplasmsDisease SusceptibilityHumansSurveys and QuestionnairesTransplantation ConditioningTransplantation, Homologous

Identifiers

PMID37898151
PMCPMC13244481
OpenAlexW4388007179

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.