Evidence map›Paper›PMID 38491198›Full record

ArticleBone marrow transplantation2024

Treosulfan compared to busulfan in allogeneic haematopoietic stem cell transplantation for myelofibrosis: a registry-based study from the Chronic Malignancies Working Party of the EBMT.

Marie Robin, Simona Iacobelli, Linda Koster, Jakob Passweg, Daniele Avenoso, Keith M O Wilson, Urpu Salmenniemi, Peter Dreger, Peter von dem Borne, John A Snowden and 15 more

Erratum issuedOpen access · greenAbstract readComparative StudyMulticenter 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. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

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  7. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors at 20 institutions in 8 countries.

Marie RobinHôpital Saint-Louis, APHP, Université de Paris Cité, Paris, France. marie.robin@aphp.fr.ORCID http://orcid.org/0000-0003-1388-9876
Simona IacobelliDeptartment of Biology, University of Rome Tor Vergata, Rome, Italy.
Linda KosterEBMT Leiden Study Unit, Leiden, The Netherlands.
Jakob PasswegUniversity Hospital | Basel, Basel, Switzerland.ORCID http://orcid.org/0000-0001-7092-3351
Daniele AvenosoKing's College Hospital, London, UK.ORCID http://orcid.org/0000-0003-4218-4170
Keith M O WilsonUniversity Hospital of Wales, Cardiff, UK.ORCID http://orcid.org/0000-0002-6327-9366
Urpu SalmenniemiHUCH Comprehensive Cancer Center, Helsinki, Finland.
Peter DregerUniversity of Heidelberg, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-7429-8570
Peter von dem BorneLeiden University Hospital, Leiden, The Netherlands.ORCID http://orcid.org/0000-0002-7470-7346
John A SnowdenSheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.ORCID http://orcid.org/0000-0001-6819-3476
Stephen RobinsonBristol Royal Hospital for Children, Bristol, UK.
Maria Chiara FinazziASST Papa Giovanni XXIII, Bergamo, Italy.
Thomas SchroederUniversity Hospital | Essen, Duesseldorf, Germany.ORCID http://orcid.org/0000-0002-1653-7959
Matthew CollinNorthern Centre for Bone Marrow Transplantation, Newcastle, England.
Matthias EderHannover Medical School, Hannover, Germany.
Edouard ForcadeService d'Hématologie Clinique et Thérapie Cellulaire, CHU Bordeaux, F-33000, Bordeaux, France.ORCID http://orcid.org/0000-0002-8873-2868
Michael LoschiCHU Nice-Hôpital de l'ARCHET, Nice, France.ORCID http://orcid.org/0000-0002-4460-5939
Stefania BramantiDepartment of Oncology/Hematology, IRCCS Humanitas Research Hospital, via Manzoni 56, Rozzano, 20089, Milan, Italy.
Jose Antonio Pérez-SimónInstituto de Biomedicina de Sevilla IBIS, CSIC, Hospital Universitario Virgen del Rocío Universidad de Sevilla, Sevilla, Spain.ORCID http://orcid.org/0000-0003-3616-6101
Tomasz CzerwMaria Skłodowska-Curie National Research Institute of Oncology, Gliwice, Poland.
Nicola PolverelliDivision of Hematology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.ORCID http://orcid.org/0000-0001-6297-9697
Joanna Drozd-SokolowskaUniversity Clinical Centre Medical University of Warsaw, Warsaw, Poland.ORCID http://orcid.org/0000-0002-4562-6264
Kavita RajUniversity College London Hospitals NHS Trust, London, UK.ORCID http://orcid.org/0000-0002-8258-354X
Juan Carlos Hernández-BoludaDepartment of Hematology, Hospital Clínico Universitario, Valencia, Spain.ORCID http://orcid.org/0000-0002-4289-3113
Donal P McLornanUniversity College Hospital London, London, UK.ORCID http://orcid.org/0000-0003-1224-091X
Bristol Royal Hospital for Children · GBDüsseldorf University Hospital · DEEuropean Society for Blood and Marrow Transplantation · NLHeidelberg University · DEHôpital l'Archet · FRHospital Clínico Universitario de Valencia · ESInstituto de Biomedicina de Sevilla · ESIRCCS Humanitas Research Hospital · ITKing's College Hospital · GBLeiden University · NLMedical University of Warsaw · PLMedizinische Hochschule Hannover · DEOspedale Papa Giovanni XXIII · ITPoliclinico San Matteo Fondazione · ITPolyclinique de Bordeaux-Tondu · FRSheffield Teaching Hospitals NHS Foundation Trust · GBThe Maria Sklodowska-Curie National Research Institute of Oncology · PLUniversité Paris Cité · FRUniversity College Hospital · GBUniversity College London Hospitals NHS Foundation Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We aimed to compare outcomes following treosulfan (TREO) or busulfan (BU) conditioning in a large cohort of myelofibrosis (MF) patients from the EBMT registry. A total of 530 patients were included; 73 received TREO and 457 BU (BU ≤ 6.4 mg/kg in 134, considered RIC, BU > 6.4 mg/kg in 323 considered higher dose (HD)). Groups were compared using adjusted Cox models. Cumulative incidences of engraftment and acute GVHD were similar across the 3 groups. The TREO group had significantly better OS than BU-HD (HR:0.61, 95% CI: 0.39-0.93) and a trend towards better OS over BU-RIC (HR: 0.66, 95% CI: 0.41-1.05). Moreover, the TREO cohort had a significantly better Progression-Free-Survival (PFS) than both the BU-HD (HR: 0.57, 95% CI: 0.38-0.84) and BU-RIC (HR: 0.60, 95% CI: 0.39-0.91) cohorts, which had similar PFS estimates. Non-relapse mortality (NRM) was reduced in the TREO and BU-RIC cohorts (HR: 0.44, 95% CI: 0.24-0.80 TREO vs BU-HD; HR: 0.54, 95% CI: 0.28-1.04 TREO vs BU-RIC). Of note, relapse risk did not significantly differ across the three groups. In summary, within the limits of a registry-based study, TREO conditioning may improve PFS in MF HSCT and have lower NRM than BU-HD with a similar relapse risk to BU-RIC. Prospective studies are needed to confirm these findings.

Indexed as

BusulfanHematopoietic Stem Cell TransplantationPrimary MyelofibrosisRegistriesAdultAgedFemaleGraft vs Host DiseaseHumansMaleMiddle AgedTransplantation ConditioningTransplantation, HomologousBusulfantreosulfan

Identifiers

PMID38491198
OpenAlexW4392861112

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.