Evidence map›Paper›PMID 42156943›Full record

ArticleBone marrow transplantation2026

The impact of pre-transplant extramedullary disease on the outcome of allogeneic hematopoietic cell transplantation for acute myeloid leukaemia in children- on behalf of PDWP/EBMT.

Juliana Silva, Jacques-Emmanuel Galimard, Jean-Hugues Dalle, Franco Locatelli, Hawazen S Alsaedi, Miguel Angel Diaz, Charlotte Jubert, Cecile Renard, Giuseppina Simone, Peter Bader and 17 more

Abstract read
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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

27 authors.

Juliana SilvaDepartment of Blood and Marrow Transplantation, Great Ormond Street Hospital, London, UK. Juliana.silva@gosh.nhs.uk.ORCID 0000-0003-1890-692X
Jacques-Emmanuel GalimardHôpital Saint-Antoine, EBMT Statistical Unit, Paris, France.ORCID 0000-0001-9102-4427
Jean-Hugues DallePediatric Hematology and Immunology Department, Hôpital Robert Debré GHU APHP Nord Université Paris Cité, Paris, France.
Franco LocatelliDepartment of Pediatric Hematology and Oncology, Ospedale Pediatrico Bambino Gesù, Catholic University of the Sacred Heart, Rome, Italy.ORCID 0000-0002-7976-3654
Hawazen S AlsaediDepartment of Pediatric Hematology-Oncology, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.ORCID 0000-0002-7478-2514
Miguel Angel DiazHematopoietic Stem Cell Transplantation & Cellular Therapy Unit, Hospital Infantil Universitario "Niño Jesús", Madrid, Spain.ORCID 0000-0001-5286-1329
Charlotte JubertCHU Bordeaux Groupe Hospitalier Pellegrin-Enfants, Bordeaux, France.
Cecile RenardUnité de coordination interne et externe, Institut d'Hematologie et d'Oncologie Pediatrique, Lyon, France.
Giuseppina SimoneAORN Santobono Pausilipon Dipartimento di Oncologia UOC TSCE e terapie cellular, Napoli, Italy.
Peter BaderDepartment of Pediatric Oncology/Hematology, Universitätsklinikum Frankfurt Goethe-Universität Klinik für Kinder- und Jugendmedizin, Frankfurt am Main, Germany.
Franca FagioliOnco-Ematologia Pediatrica, Centro Trapianti Cellule Staminali, Ospedale Infantile Regina Margherita, Piazza Polon, Turin, Italy.ORCID 0000-0002-9257-900X
Vassiliki Kitra RoussouSt Sophia Children's Hospital Oncology Centre "Marianna v. Vardinogiannis - Elpida", BMT Unit, Athens, Greece.
Caroline L FurnessDepartment of Paediatric Oncology, Royal Marsden Hospital, London, UK.
Robert WynnDept. of Blood and Marrow Transplantation, Royal Manchester Children's Hospital, Manchester, UK.ORCID 0000-0002-6046-8428
Birgit BurkhardtPediatric Hematology and Oncology, University Hospital Münster, Münster, Germany.ORCID 0000-0002-1151-829X
Alessandra BiffiPediatric Hematology, Oncology, and Stem Cell Transplant Division, Padua University and Hospital, Padua, Italy.ORCID 0000-0002-4610-0870
Marc BieringsPrincess Maxima Center/ University Hospital for Children (WKZ), Stem cell transplantation, Utrecht, Netherlands.ORCID 0000-0002-0192-3080
Cristina Díaz de HerediaPediatric Oncology and Hematology Department, Hospital Universitari Vall d'Hebron Vall d'Hebron, Barcelona, Spain.ORCID 0000-0001-8086-296X
Arcangelo PreteDepartment of Pediatrics, University of Bologna Sant'Orsola-Malpighi Hospital, SSD Oncoematologia Pediatrica, IRCCS-AOU di Bologna, Policlinico S. Orsola, Bologna, Italy.
Amos TorenThe Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Israel.
Katharine PatrickSheffield Childrens NHS Foundation Trust, Department of Pediatric Haematology, Sheffield, UK.
Wolfgang HolterSt. Anna Kinderspital, Stem Cell Transplantation Unit, Vienna, Austria.
Krzysztof KalwakDepartment of Pediatric Hematology, Oncology and Bone Marrow Transplantation, Wroclaw Medical University, Wroclaw, Poland.ORCID 0000-0003-1174-5799
Arnaud DalissierHôpital Saint-Antoine, EBMT Paris Study Unit, Paris, France.
Kanchan Rao *Department of Blood and Marrow Transplantation, Great Ormond Street Hospital, London, UK.ORCID 0000-0001-9449-8476
Selim Corbacioglu *Department of Pediatric Hematology, Oncology and Stem Cell Transplantation, University of Regensburg, Regensburg, Germany.ORCID 0000-0003-1070-8486
Paediatric Disease Working Party of European Society of Bone marrow Transplant (PDWP/EBMT)

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extramedullary disease (EMD) is a rare presentation in Acute Myeloid Leukaemia (AML). On behalf of PDWP/EBMT we studied the effect of EMD compared to isolated BM involvement in the outcomes following non-TBI conditioning hematopoietic stem cell transplantation (HCT) for AML in children. Patients were grouped into three categories: BM involvement only (Group A), BM + CNS involvement only (Group B) and BM+ other EMD+/- CNS (Group C). A total of 958 patients were included, 685 (71.5%) in Group A, 135 (14.1%) in Group B and 138 (14.4%) in Group C. The median post HCT follow-up was 5.4 years. Five years LFS, OS, RI and NRM were 62%, 68.4%, 26.4% and 11.6%, respectively. Multivariate analysis showed higher RI in Group C compared to Group A (HR = 1.45 (1.01-2.06) p = 0.04). In the multivariate analysis patients with EMD had no significant difference in LFS, OS and NRM. Our findings suggest that children with AML and BM with EMD+/- CNS involvement (group C) have a higher incidence of relapse after HCT compared to those with BM only or BM + CNS only disease. However, the presence of EMD did not have an impact on overall, leukaemia-free survival or non-relapse mortality.

Indexed as

Hematopoietic Stem Cell TransplantationLeukemia, Myeloid, AcuteTransplantation ConditioningAdolescentChildChild, PreschoolDisease-Free SurvivalFemaleHumansInfantMaleRetrospective StudiesTransplantation, HomologousTreatment Outcome

Identifiers

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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.