Evidence map›Paper›PMID 42469396›Full record

ArticleBone marrow transplantation2026

Impact of conditioning regimen on outcomes of young AML patients ( < 40 years) undergoing HCT in complete remission, with transplant conditioning intensity score of 3.5-4.0. A study from the acute leukemia working party of the European Society for Blood and Marrow Transplantation.

Enrico Maffini, Maud Ngoya, Mohamed Houhou, Malek Benakli, Babak Bahar, Mahmoud Aljurf, Khalid Halahleh, Regis Peffault de Latour, Igor-Wolfgang Blau, Andrew Clark and 16 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

26 authors.

Enrico MaffiniIRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy. enrico.maffini@aosp.bo.it.ORCID http://orcid.org/0000-0001-7356-2328
Maud NgoyaEBMT ALWP Statistical Unit, Paris, France.ORCID http://orcid.org/0000-0002-7810-6900
Mohamed HouhouEBMT ALWP Statistical Unit, Paris, France.
Malek BenakliPierre and Marie Curie Center, University of Health Sciences, Alger, Algeria.ORCID http://orcid.org/0000-0001-8444-890X
Babak BaharShariati Hospital, Hematology-Oncology and BMT Research-Teheran, Teheran, Iran.
Mahmoud AljurfKing Faisal Specialist Hospital & Research Centre, Riyad, Saudi Arabia.ORCID http://orcid.org/0000-0003-3942-7370
Khalid HalahlehKing Hussein Cancer Center, Adult Bone Marrow Transplantation and Cellular Therapy Program, Amman, Jordan.ORCID http://orcid.org/0000-0002-1161-9138
Regis Peffault de LatourHematology and Transplantation Unit, Hôpital Saint Louis, AP-HP, Paris, France.
Igor-Wolfgang BlauMedizinische Klinik m. S. Hamatologie, Onkologie und Tumorimmunologie, Berlin, Germany.
Andrew ClarkBMT Unit, Queen Elizabeth University Hospital Glasgow, Glasgow, United Kingdom.
Catherine FlynnTrinity St James Cancer Institute, Dublin, Ireland.
Peter Pal RemenyiDel-pesti Centrumkorhaz, Budapest, Hungary, Budapest, Hungary.
Maria Losa MarotoBirmingham Centre for Cellular Therapy and Transplant (BCCTT), Birmingham, United Kingdom.
Ibrahim Yakoub-AghaCHU de Lille, Universitè Lille, INSERM U1286, Infinite, Lille, France.ORCID http://orcid.org/0000-0003-4524-8782
Henrik SengeloevRigshospitalet, Copenhagen, Denmark.
Cristina Castilla-LlorenteInstitut Gustave Roussy, Villejuif, France.ORCID http://orcid.org/0000-0002-7728-5804
Emma NicholsonRoyal Marsden Hospital, London, United Kingdom.ORCID http://orcid.org/0000-0002-6439-0795
Urpu SalmenniemiHUCH Comprehensive Cancer Center, Helsinki, Finland.
Radovan VrhovacUniversity Hospital Centre, Zagreb, Croatia.ORCID http://orcid.org/0000-0003-3323-3487
Jakob PasswegUniversity Hospital Basel, Basel, Switzerland.ORCID http://orcid.org/0000-0001-7092-3351
Matthias EderMedical School Hannover, Hannover, Germany.ORCID http://orcid.org/0009-0000-3362-5814
Etienne DaguindauHopital Jean Minjoz, Besancon, France.
Alexandros SpyridonidisHematology Division, Department of Internal Medicine, University of Patras, Medical School, Patras, Greece.ORCID http://orcid.org/0000-0003-3097-2532
Arnon NaglerDivision of Hematology, Sheba Medical Center, Tel Hashomer, Tel Aviv, Israel.ORCID http://orcid.org/0000-0002-0763-1265
Fabio CiceriIRCCS Ospedale San Raffaele, Milano, Italy.ORCID http://orcid.org/0000-0003-0873-0123
Mohamad MohtySorbonne University, Clinical Hematology and Cellular Therapy Department, Saint Antoine Hospital, INSERM UMRs 938, Paris, France.ORCID http://orcid.org/0000-0002-7264-808X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The optimal myeloablative conditioning regimen for adolescents and young adults with acute myeloid leukaemia (AML) is currently unknown. In this retrospective analysis conducted on AML patients aged 18-40 years, in complete remission (CR), who received an allogeneic hematopoietic cell transplantation (HCT) we compared outcomes of different conditioning regimens. A total of 4323 patients, with median age of 30.9 years, transplanted from 2010 to 2022, received one of four regimens: high-dose total body irradiation (TBI)-based (n = 1031), thiotepa-busulfan (Bu)-fludarabine (Flu) (TBF) n = 219, Bu-Flu (n = 1100), and Bu-cyclophosphamide (Cy) (n = 1973). Prolonged OS and PFS for Bu-Flu (hazard ratio [HR] 0.73, 95% CI 0.57-0.92, p = 0.008; HR 0.78, 95% CI 0.64-0.94, p = 0.01), and TBF (HR 0.59, 95% CI 0.38-0.92, p = 0.02; HR 0.67, 95% CI 0.47-0.94, p = 0.02), respectively, as well as less RI for both Bu-Flu (HR 0.77, 95% CI 0.63-0.95, p = 0.01), and TBF (HR 0.68, 95% CI 0.47-0.99, p = 0.046). In conclusion, young adult AML patients seem to benefit from high dose TBI-free regimens, in terms of survival and toxicity, with four major myeloablative regimens. TBF and Bu-Flu were associated with better clinical outcomes, partly reflecting the general improvement in supportive therapies and patient selection introduced in recent years. Prospective clinical trials are warranted.

Indexed as

Hematopoietic Stem Cell TransplantationLeukemia, Myeloid, AcuteTransplantation ConditioningAdolescentAdultFemaleHumansMaleRemission InductionRetrospective StudiesTreatment OutcomeYoung Adult

Identifiers

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Registered trials

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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 Socratic graph.