Evidence map›Paper›PMID 41963641›Full record

ArticleBone marrow transplantation2026

Management of tyrosine kinase inhibitors and donor lymphocyte infusions post transplantation for chronic myeloid leukemia: a survey of contemporary practice on behalf of the chronic malignancies working party of the EBMT.

Alexandros Kanellopoulos, Linda Koster, Hugues de Lavallade, Guillermo Ortí, Sebastian Francis, Jakob Passweg, Jane Apperley, Wolfgang Bethge, Werner Rabitsch, Jennifer Clay and 21 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

31 authors.

Alexandros KanellopoulosDepartment of Haematology, Sheffield Teaching Hospitals, Sheffield, United Kingdom. alexandros.kanellopoulos@nhs.net.
Linda KosterEBMT Leiden Study Unit, Leiden, the Netherlands.
Hugues de LavalladeDepartment of Haematology, Guy's and St, Thomas' NHS Foundation Trust, London, UK.ORCID 0000-0002-4988-2564
Guillermo OrtíDepartment of Hematology, Vall d'Hebron University Hospital, Vall d'Hebron Institute of Oncology, Barcelona, Spain.ORCID 0000-0002-7889-5807
Sebastian FrancisDepartment of Haematology, Sheffield Teaching Hospitals, Sheffield, United Kingdom.
Jakob PasswegUniversity Hospital | Basel, Basel, Switzerland.ORCID 0000-0001-7092-3351
Jane ApperleyImperial College Healthcare NHS Trust, London, UK.ORCID 0000-0002-1710-1794
Wolfgang BethgeUniversity Hospital Tuebingen, Department of Hematology & Oncology, Tübingen, Germany.ORCID 0000-0001-6052-2618
Werner RabitschInternal Medicine I, BMT-Unit, Medical University of Vienna, Vienna, Austria.
Jennifer ClaySt James Hospital, Leeds, UK.
Edouard ForcadeCHU Bordeaux, Pessac, France.ORCID 0000-0002-8873-2868
Erin HurstFreeman Hospital, Newcastle Upon Tyne, UK.
Caroline BesleyBristol Haematology & Oncology Centre, Bristol, UK.
Francesca KinsellaUniversity Hospitals Birmingham, Birmingham, UK.
Mahmoud AljurfKing Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.ORCID 0000-0003-3942-7370
He HuangThe First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Aloysius HoSingapore General Hospital, Singapore, Singapore.ORCID 0000-0003-1299-8560
Inken HilgendorfUniversitätsklinikum Jena, Klinik für Innere Medizin II, Abteilung für Hämatologie und medizinische Onkologie, Jena, Germany.ORCID 0000-0003-2038-9730
Goda ChoiUniversity Medical Center Groningen (UMCG), Groningen, The Netherlands.
Francis AyukUniversity Medical Center Hamburg, Hamburg, Germany.
Helbig GrzegorzDepartment of Hematology and Bone Marrow Transplantation, Medical University of Silesia, Katowice, Poland.
Matthias StelljesUniversity Hospital of Muenster, Münster, Germany.ORCID 0000-0002-9331-5145
Deborah RichardsonUniversity Hospital Southampton, Southampton, UK.ORCID 0000-0002-8858-923X
Elena MorozovaPavlov University, Saint-Petersburg, Russian Federation.ORCID 0000-0002-9605-485X
Witold PrejznerUniversity Clinical Center, Gdańsk, Poland.
Robert ZeiserUniversity Hospital Freiburg, Freiburg, Germany.ORCID 0000-0001-6565-3393
Christopher ArmstrongDepartment of Haematology, St. James Hospital, Dublin, Ireland.ORCID 0000-0001-5704-7895
Kavita RajDepartment of Haematology and Cellular Therapy, University College Hospital, London, UK.ORCID 0000-0002-8258-354X
Joanna Drozd-SokolowskaCentral Clinical Hospital, The Medical University of Warsaw, Warsaw, Poland.ORCID 0000-0002-4562-6264
Yves ChalandonHematology Division and Faculty of Medicine, Hopitaux Universitaires de Geneve, University of Geneva, Geneva, Switzerland.ORCID 0000-0001-9341-8104
Donal P McLornanDepartment of Haematology and Cellular Therapy, University College Hospital, London, UK.ORCID 0000-0003-1224-091X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The landscape of Allogeneic Haematopoietic Cell Transplantation (allo-HCT) for Chronic Myeloid Leukaemia (CML) remains dynamic with the advent of tyrosine kinase inhibitors (TKIs). There remains an absence of widely agreed evidence-based guidelines for post-transplant monitoring and relapse management. To evaluate current real-world practices for 'high risk' CML, the CML subcommittee of the Chronic Malignancies Working Party (CMWP) of the European Blood and Marrow Transplantation (EBMT) society developed an electronic survey, which was distributed to 39 EBMT-registered transplant centres in April 2024. Centres were chosen based on CML allo-HCT activity. Twenty-three centres (59%) responded, providing clinical perspectives into pre-transplant chemotherapy regimens, TKI use, ABL1 kinase domain mutation analysis, post-transplant monitoring, and their practice regarding sequencing/ integration of TKIs with donor lymphocyte infusions (DLI). Most centres conduct monthly BCR::ABL1 transcript monitoring during the first three months post-transplant, transitioning to quarterly assessments upon achieving a deep molecular response. TKI maintenance is widely adopted across centres, with treatment duration guided by molecular response, and TKIs are generally preferred over DLI for managing molecular relapse. However, DLI remains a valid option for TKI-refractory chronic-phase (CP)-CML relapse. Survey findings illustrate significant heterogeneity in practice, offering insights to inform research aimed at improving allo-HCT outcomes in CML.

Indexed as

Hematopoietic Stem Cell TransplantationLeukemia, Myelogenous, Chronic, BCR-ABL PositiveLymphocyte TransfusionProtein Kinase InhibitorsHumansSurveys and QuestionnairesProtein Kinase Inhibitors

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

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.