Evidence map›Paper›PMID 32892216›Full record

ArticleBone marrow transplantation2021

Total body irradiation + fludarabine compared to busulfan + fludarabine as "reduced-toxicity conditioning" for patients with acute myeloid leukemia treated with allogeneic hematopoietic cell transplantation in first complete remission: a study by the Acute Leukemia Working Party of the EBMT.

Sebastian Giebel, Myriam Labopin, Malgorzata Sobczyk-Kruszelnicka, Matthias Stelljes, Jenny L Byrne, Nathalie Fegueux, Dietrich W Beelen, Montserrat Rovira, Alexandros Spyridonidis, Didier Blaise and 6 more

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Article in Bone marrow transplantation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 19% 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

3 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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

16 authors at 20 institutions in 24 countries.

Sebastian GiebelDepartment of Bone Marrow Transplantation and Onco-Hematology, Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice Branch, Gliwice, Poland. sgiebel@io.gliwice.pl.ORCID http://orcid.org/0000-0002-4827-4401
Myriam LabopinEuropean Society for Blood and Marrow Transplantation Paris Study Office/CEREST-TC, Paris, France.ORCID http://orcid.org/0000-0003-4514-4748
Malgorzata Sobczyk-KruszelnickaDepartment of Bone Marrow Transplantation and Onco-Hematology, Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice Branch, Gliwice, Poland.ORCID http://orcid.org/0000-0002-2007-7609
Matthias StelljesDepartment of Hematology and Oncology, University Hospital of Münster, University of Münster, Münster, Germany.
Jenny L ByrneFaculty of Medicine and Health Sciences, University of Nottingham, Nottingham, UK.
Nathalie FegueuxDepartment of Hematology, CHU Lapeyronie, Montpellier, France.
Dietrich W BeelenDepartment of Bone Marrow Transplantation, West German Cancer Centre, University Hospital of Essen, University of Duisburg, Essen, Germany.
Montserrat RoviraHSCT Unit, Hematology Department, Hospital Clínic de Barcelona, University of Barcelona, Barcelona, Catalunya, Spain.
Alexandros SpyridonidisDepartment of Internal Medicine, Bone Marrow Transplantation Unit, University Hospital of Patras, Patras, Greece.ORCID http://orcid.org/0000-0003-3097-2532
Didier BlaiseProgramme de Transplantation & Therapie Cellulaire, Centre de Recherche en Cancérologie de Marseille, Institut Paoli Calmettes, Marseille, France.ORCID http://orcid.org/0000-0002-5684-9447
Martin BornhäuserDepartment of Internal Medicine I, University Hospital Carl Gustav Carus, Dresden, Germany.
Ihsan KaradoganDivision of Hematology, Antalya Medstar Hospital, Antalya, Turkey.
Bipin N SavaniDivision of Hematology and Oncology, Vanderbilt University Medical Center, Nashville, TN, USA.ORCID http://orcid.org/0000-0002-3304-9965
Arnon NaglerHematology Division, Chaim Sheba Medical Center, Tel-Hashomer, Israel.ORCID http://orcid.org/0000-0002-0763-1265
Mohamad MohtyDepartment of Hematology, Hospital Saint Antoine, Paris, France.
Principal investigators of the contributing institutions
American University of Beirut Medical Center · LBAndalusian Health Service · ESBiogipuzkoa Health Research Institute · ESCentre Hospitalier Régional et Universitaire de Nancy · FRCentre Hospitalier Universitaire de Grenoble · FRCharles University · CZDeutsche Klinik für Diagnostik · DEGoethe University Frankfurt · DEHeidelberg University · DEHôpital Cardiologique du Haut-Lévêque · FRHôpital Necker-Enfants Malades · FRHospital General Universitario Gregorio Marañón · ESInserm · FRInstytut Hematologii i Transfuzjologi · PLKing Hussein Cancer Center · JOKlinikum Magdeburg · DEOslo University Hospital · NOQueen Elizabeth Hospital Birmingham · GBRobert Bosch Hospital · DESingapore General Hospital · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The optimal conditioning for patients with acute myeloid leukemia in first complete remission treated with allogeneic hematopoietic cell transplantation (allo-HCT) has not been defined so far. In this retrospective study, we compared two "reduced-toxicity" regimens: intravenous busulfan at a total dose of 9.6 mg/kg (3 days) + fludarabine (Bu3/Flu) and total body irradiation at a dose of 8 Gy + fludarabine (TBI8Gy/Flu). In the entire study cohort (n = 518), the probabilities of overall survival (OS), leukemia-free survival (LFS), relapse and non-relapse mortality (NRM) at 2 years for Bu3/Flu and TBI8Gy/Flu were 62% vs. 72.5% (p = 0.051), 59.5% vs. 65% (p = 0.15), 30% vs. 20% (p = 0.01), and 10% vs. 14% (p = 0.18), respectively. In multivariate model for patients <50 years old, TBI8Gy/Flu was associated with improved LFS (hazard ratio (HR) = 0.5, p = 0.04), OS (HR = 0.31, p = 0.004), and survival free from both graft-versus-host disease and relapse (HR = 0.55, p = 0.03), as well as tendency to reduced risk of relapse (HR = 0.53, p = 0.08). Among patients aged 50 years or older the use of TBI8Gy/Flu was associated with increased incidence of NRM (HR = 3.9, p = 0.0009), with no significant impact on other outcome measures. We conclude that the use of TBI8Gy/Flu as "reduced-toxicity" regimen may be advised in younger patients with AML referred for allo-HCT.

Indexed as

Graft vs Host DiseaseHematopoietic Stem Cell TransplantationLeukemia, Myeloid, AcuteBusulfanHumansMiddle AgedRetrospective StudiesTransplantation ConditioningVidarabineWhole-Body IrradiationBusulfanfludarabineVidarabine

Identifiers

PMID32892216
OpenAlexW3083549720

What OpenQuestion holds

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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 OpenQuestion graph.