Evidence map›Paper›PMID 38195984›Full record

ArticleBone marrow transplantation2024

Allogeneic haematopoietic cell transplantation for therapy-related myeloid neoplasms arising following treatment for lymphoma: a retrospective study on behalf of the Chronic Malignancies Working Party of the EBMT.

Mitja Nabergoj, Diderik-Jan Eikema, Linda Koster, Uwe Platzbecker, Katja Sockel, Jürgen Finke, Nicolaus Kröger, Edouard Forcade, Arnon Nagler, Matthias Eder and 17 more

Open access · greenAbstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Bone marrow transplantation, 2024. 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
1.4field-weighted citation impact, top 20% 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, 3 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

27 authors at 20 institutions in 10 countries.

Mitja NabergojHematology Service, Institut Central des Hôpitaux (ICH), Hôpital du Valais, Sion, Switzerland. mitja.nabergoj@hopitalvs.ch.ORCID 0000-0003-2842-3198
Diderik-Jan EikemaEBMT Statistical Unit, Leiden, The Netherlands.
Linda KosterEBMT Leiden Study Unit, Leiden, The Netherlands.
Uwe PlatzbeckerMedical Clinic and Policinic 1, Leipzig, Germany.ORCID 0000-0003-1863-3239
Katja SockelDepartment of Internal Medicine I, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.
Jürgen FinkeUniversity of Freiburg, Freiburg, Germany.ORCID 0000-0002-1799-5927
Nicolaus KrögerDepartment for Stem Cell Transplantation, University Medical Center Hamburg, Hamburg, Germany.ORCID 0000-0001-5103-9966
Edouard ForcadeCHU Bordeaux, Pessac, France.ORCID 0000-0002-8873-2868
Arnon NaglerChaim Sheba Medical Center, Tel-Hashomer, Israel.ORCID 0000-0002-0763-1265
Matthias EderHannover Medical School, Hannover, Germany.
Johanna TischerKlinikum Grosshadern, Munich, Germany.ORCID 0000-0003-1821-1976
Annoek E C BroersErasmus MC Cancer Institute, Rotterdam, The Netherlands.
Jürgen KuballUniversity Medical Centre, Utrecht, The Netherlands.ORCID 0000-0002-3914-7806
Keith M O WilsonUniversity Hospital of Wales, Cardiff, UK.ORCID 0000-0002-6327-9366
Mathilde Hunault-BergerCHRU, Angers, France.ORCID 0000-0001-7777-5216
Matthew CollinAdult HSCT unit, Newcastle, UK.
Domenico RussoUnit of Bone Marrow Transplantation, University of Brescia, ASST Spedali Civili, Brescia, Italy.
Lucía López CorralHematology Department, Hospital Universitario de Salamanca, IBSAL, CIBERONC Centro de Investigación del Cáncer-IBMCC (USAL-CSIC), Salamanca, Spain.
Grzegorz HelbigSilesian Medical Academy, Katowice, Poland.
Alberto MussettiInstitut Català d'Oncologia-Hospital Duran i Reynals, Barcelona, Spain.
Christof ScheidUniversity of Cologne, Cologne, Germany.
Carmelo GurnariDepartment of Biomedicine and Prevention, University of Rome Tor Vergata, 00133, Rome, Italy.ORCID 0000-0001-6829-5544
Kavita RajDepartment of Haematology, University College London Hospitals NHS Trust, London, UK.ORCID 0000-0002-8258-354X
Joanna Drozd-SokolowskaUniversity Clinical Centre, Medical University of Warsaw, Warsaw, Poland.ORCID 0000-0002-4562-6264
Ibrahim Yakoub-AghaCHU de Lille, Univ Lille, INSERM U1286, Infinite, 59000, Lille, France.ORCID 0000-0003-4524-8782
Marie RobinHopital Saint- Louis, APHP, Université de Paris Cité, Paris, France.ORCID 0000-0003-1388-9876
Donal P McLornanDepartment of Haematology, University College London Hospitals NHS Trust, London, UK.ORCID 0000-0003-1224-091X
European Society for Blood and Marrow Transplantation · NLUniversity College London Hospitals NHS Foundation Trust · GBCentre Hospitalier Universitaire d'Angers · FRCentre Hospitalier Universitaire de Bordeaux · FRErasmus MC Cancer Institute · NLHôpital du Valais · CHInserm · FRInstitut Català d'Oncologia · ESInstituto de Investigación Biomédica de Salamanca · ESLMU Klinikum · DEMedical University of Warsaw · PLMedizinische Hochschule Hannover · DESheba Medical Center · ILUniversität Hamburg · DEUniversité Paris Cité · FRUniversity Hospital Carl Gustav Carus · DEUniversity Hospital Leipzig · DEUniversity Hospital of Wales · GBUniversity Medical Center Utrecht · NLUniversity of Brescia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Therapy-related myeloid neoplasms (t-MN), either myelodysplastic neoplasms (t-MDS) or acute myeloid leukemias (t-AML), have a poor prognosis and allogeneic haematopoietic cell transplantation (allo-HCT) represents the only curative option. In this multicenter, registry-based study, we analyzed outcomes of 378 patients undergoing first allo-HCT between 2006-2017 for t-MN arising secondary to lymphoma treatment. Median age was 58 years at allo-HCT; 222 (59%) had a diagnosis of t-MDS and 156 (41%) of t-AML, respectively. At the time of allo-HCT, 46% of t-MN cases were reported as in complete remission (CR) and 15% of lymphomas were recorded as not in remission. A reduced intensity conditioning regimen was used in 70% of cases. For the entire cohort, 5-year OS, and t-MN PFS, relapse incidence and NRM were 32%, 28%, 35% and 37%, respectively. In multivariable analysis, undergoing allo-HCT with t-MN not in CR and older age were associated with significantly worse OS, PFS and NRM. At 5 years post allo-HCT, the relapse incidence of lymphoma was low at 3%, while the rate of secondary malignancies was 8%. This analysis shows the curative potential of allo-HCT for patients with t-MN arising secondary to lymphoma treatment in approximately a third of patients.

Indexed as

Graft vs Host DiseaseHematopoietic Stem Cell TransplantationLeukemia, Myeloid, AcuteLymphomaNeoplasms, Second PrimaryHumansMiddle AgedRecurrenceRetrospective StudiesTransplantation Conditioning

Identifiers

PMID38195984
OpenAlexW4390706509

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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.