Evidence map›Paper›PMID 42020760›Full record

ArticleBone marrow transplantation2026

Outcomes of 544 Patients with t(6;9)/DEK::NUP214 acute myeloid leukemia undergoing allogeneic stem cell transplantation: an EBMT study on behalf of the acute leukemia working party (ALWP) and the pediatric diseases working party (PDWP).

Fabio Andreozzi, Jacques-Emmanuel Galimard, Johan Maertens, Mahmoud Aljurf, Katherine Clesham, Jaime Sanz, Sebastien Maury, Sandrine Loron, Jakob Passweg, Thomas Schroeder and 13 more

Abstract read
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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

23 authors.

Fabio AndreozziInstitut Jules Bordet - HUB, Bruxelles, Belgium. fabio.andreozzi@hubruxelles.be.ORCID 0000-0002-6549-7367
Jacques-Emmanuel GalimardEBMT Paris Study Unit, Sorbonne University, Saint-Antoine Hospital, AP-HP, INSERM UMRs 938, Paris, France.ORCID 0000-0001-9102-4427
Johan MaertensUniversity Hospital Gasthuisberg, Leuven, Belgium.ORCID 0000-0003-4257-5980
Mahmoud AljurfKing Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia.ORCID 0000-0003-3942-7370
Katherine CleshamUniversity College London Hospital, London, UK.
Jaime SanzHematology Department, Hospital Universitari i Politècnic La Fe, Valencia Departament de Medicina Universitat de Valencia, CIBERONC, Instituto Carlos III, Madrid, Spain.ORCID 0000-0001-6934-4619
Sebastien MauryHopital Henri Mondor, Creteil, France.
Sandrine LoronCentre Hospitalier Lyon Sud, Pierre Bénite, France.
Jakob PasswegUniversity Hospital, Basel, Switzerland.ORCID 0000-0001-7092-3351
Thomas SchroederUniversity Hospital Essen, Essen, Germany.
Urpu SalmenniemiHUS Comprehensive Cancer Center, Helsinki, Finland.
Gwendolyn van GorkomDepartment of Internal Medicine, Division of Hematology, GROW School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, The Netherlands.ORCID 0000-0001-7327-7834
Regis Peffault de LatourSaint-Louis Hospital, BMT Unit, Université Paris Cité, Paris, France.
Peter A von dem BorneLeiden University Hospital, Leiden, Netherlands.ORCID 0000-0002-7470-7346
Franco LocatelliIRCCS Ospedale Pediatrico Bambino Gesu, Catholic University of the Sacred Heart, Rome, Italy.ORCID 0000-0002-7976-3654
Robert F WynnRoyal Manchester Children's Hospital, Manchester, UK.ORCID 0000-0002-6046-8428
Jean-Hugues DalleHopital Robert Debre Pediatric, Paris, France.
Jordi EsteveInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.ORCID 0000-0002-8056-648X
Arnon NaglerChaim Sheba Medical Center, Tel-Hashomer, Israel.ORCID 0000-0002-0763-1265
Katharina KleinschmidtDepartment of Pediatric Hematology, Oncology and Stem Cell Transplantation, University Hospital Regensburg, Regensburg, Germany.ORCID 0000-0002-1447-7286
Mohamad MohtySorbonne University Paris INSERM, Saint-Antoine Research Centre, Paris, France.ORCID 0000-0002-7264-808X
Krzysztof Kalwak *Clinical Department of Paediatric BMT, Wroclaw Medical University, Wroclaw, Poland.ORCID 0000-0003-1174-5799
Fabio Ciceri *IRCCS San Raffaele Hospital Scientific Institute, Milano, Italy.ORCID 0000-0003-0873-0123

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute myeloid leukemia (AML) with translocation (6;9)(p23;q34) is a rare and high-risk disease, frequently co-occurring with FLT3-ITD alteration. We retrospectively analyzed 544 patients with t(6;9) AML undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT) and reported to the EBMT registry, between 2000 and 2022. At 2-years, overall survival (OS), leukemia-free survival (LFS), relapse incidence (RI), non-relapse mortality (NRM) and GVHD-free/relapse-free survival (GRFS) were 65.7%, 59.1%, 23.0%, 17.9% and 45.6% respectively. The 431 patients transplanted in first complete remission (CR1) had more favorable OS (71.7%), LFS (65.8%) and RI (18.2%). Pediatric and adolescent/young adult (AYA, ≤ 39 years) patients in CR1 had improved outcomes. In patients ≥ 40 years old, OS, LFS, and NRM gradually worsened, whereas significant increase in RI and decrease in GRFS were observed after 53 years. In a matched-pair analysis performed on 76 FLT3-ITD positive and 76 negative CR1 patients, FLT3-ITD was associated with an approximately three-fold higher RI risk, without differences in OS. In conclusion, allo-HSCT in t(6;9) AML provides relatively favorable outcomes especially when performed in CR1. Pediatric and AYA patients derived the greatest benefit from transplant. FLT3-ITD positivity remains a relevant risk factor for relapse, though without impact on OS.

Indexed as

Hematopoietic Stem Cell TransplantationLeukemia, Myeloid, AcuteNuclear Pore Complex ProteinsTranslocation, GeneticAdolescentAdultAllograftsChildChild, PreschoolDisease-Free SurvivalFemaleHumansInfantMaleMiddle AgedRetrospective StudiesNuclear Pore Complex ProteinsNUP214 protein, human

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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.