Evidence map›Paper›PMID 41714405›Full record

ArticleLeukemia2026

Development of a prognostic scoring system for chronic myeloid leukemia in blast phase.

Michael Lauseker, Tomasz Sacha, Hana Klamova, Julia Yakoleva, Elza Lomaia, Dragana Milojkovic, Christian Fabisch, Franck E Nicolini, Ulla Olsson-Stromberg, Daniela Zackova and 31 more

Abstract read
In one paragraph

Article in Leukemia, 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
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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

41 authors.

Michael LausekerInstitut für Medizinische Informationsverarbeitung, Biometrie und Epidemiologie (IBE), Medizinische Fakultät, Ludwig-Maximilians-Universität München, Munich, Germany. lauseker@ibe.med.uni-muenchen.de.ORCID http://orcid.org/0000-0002-6662-7127
Tomasz SachaJagiellonian University Medical College, Department of Hematology, Krakow, Poland.ORCID http://orcid.org/0000-0002-7207-6595
Hana KlamovaInstitute of Hematology and Blood Transfusion, Prague, Czech Republic.ORCID http://orcid.org/0009-0000-5020-7040
Julia YakolevaRM Gorbacheva Research Institute, Pavlov University, Saint Petersburg, Russia.
Elza LomaiaResearch Department of Immuno-Oncology, Almazov National Medical Research Centre, Saint Petersburg, Russian Federation.ORCID http://orcid.org/0000-0003-3290-7961
Dragana MilojkovicHammersmith Hospital, Imperial College NHS Trust, London, UK.
Christian FabischKlinik für Innere Medizin II, Universitätsklinikum Jena, Jena, Germany.
Franck E NicoliniCentre Léon Bérard, Hématology Department, Lyon, France.
Ulla Olsson-StrombergUniversity Hospital Uppsala, Department of Hematology, Uppsala, Sweden.
Daniela ZackovaDepartment of Internal Medicine, Hematology and Oncology, University Hospital Brno and Masaryk University, Brno, Czech Republic.
Krzysztof LewandowskiDepartment of Hematology & Bone Marrow Transplantation, Poznań University of Medical Sciences, Poznań, Poland.
Philipp ErnstKlinik für Innere Medizin II, Universitätsklinikum Jena, Jena, Germany.ORCID http://orcid.org/0000-0001-5165-9874
Fausto CastagnettiIRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli", Bologna, Italy.ORCID http://orcid.org/0000-0002-0602-2628
Klaus HirschbühlHematology and Oncology, Faculty of Medicine, University of Augsburg, Augsburg, Germany.ORCID http://orcid.org/0000-0002-4847-7460
Irena ZupanDepartment of Haematology, University Medical Centre Ljubljana, Ljubljana, Slovenia.
Astghik VoskanyanHematology Center after Prof. R. Yeolyan, Yerevan, Armenia.
Aleksandra GołosHematooncology Department, Copernicus Memorial Hospital, Lodz, Poland.
Jochen J FrietschMedizinischen Klinik und Poliklinik II, Uniklinikum Würzburg, Würzburg, Germany.ORCID http://orcid.org/0000-0002-1476-8059
Justyna GilOncology Centre of the Podkarpackie Province, Department of Hematooncology, Brzozow, Poland.
Edgar FaberDepartment of Hemato-Oncology, University Hospital Olomouc, Faculty of Medicine and Dentistry, Palacky University in Olomouc, Olomouc, Czech Republic.ORCID http://orcid.org/0000-0002-3259-7791
Stefan W KrauseUniklinik Erlangen, Medizinische Klinik 5, Erlangen, Germany.ORCID http://orcid.org/0000-0002-5259-4651
Anne ParryCentre Hospitalier Annecy Genevois, Annecy, France.
Susanne SausseleIII. Med. Klinik, Med. Fakultät Mannheim, Universität Heidelberg, Mannheim, Germany.ORCID http://orcid.org/0000-0003-0357-5785
Sonja HeiblAbteilung für Innere Medizin IV, Klinikum Wels-Grieskirchen, Wels, Austria.
Georg-Nikolaus FrankeUniversity of Leipzig Medical Center, Department of Hematology, Cellular Therapy, Hemostaseology and Infectious Diseases, Leipzig, Germany.ORCID http://orcid.org/0000-0001-8239-002X
Luis Felipe CasadoServicio de Hematología, Hospital General Universitario de Toledo, Toledo, Spain.
Edyta PaczkowskaDepartment of General Pathology, Pomeranian Medical University in Szczecin, Szczecin, Poland.ORCID http://orcid.org/0000-0001-7052-9741
Holger HebartZentrum für Innere Medizin, Hämatologie/Onkologie, Stauferklinikum Schwäbisch-Gmünd, Mutlangen, Germany.ORCID http://orcid.org/0000-0003-4536-9955
Matthias EderKlinik für Hämatologie, Hämostaseologie, Onkologie und Stammzelltransplantation, Medizinische Hochschule Hannover, Hannover, Germany.
Peter AnhutOnkologische Schwerpunktpraxis Anhut, Kronach, Germany.
Karolin Trautmann-GrillMedizinische Klinik I, Universitätsklinikum Carl Gustav Carus, TU Dresden, Dresden, Germany.ORCID http://orcid.org/0000-0002-9050-1049
Elzbieta SzczepanekJagiellonian University Medical College, Department of Hematology, Krakow, Poland.
Thomas SüdhoffKlinikum Passau, Klinik für Onkologie, Hämatologie und Palliativmedizin, Passau, Germany.
Elzbieta PatkowskaHematology Department, Institute of Hematology and Transfusion Medicine, Warsaw, Poland.
Alexander KianiMedizinische Klinik IV, Klinikum Bayreuth GmbH, Bayreuth, and Comprehensive Cancer Center Erlangen-EMN, Bayreuth, Germany.
Thomas ErnstKlinik für Innere Medizin II, Universitätsklinikum Jena, Jena, Germany.ORCID http://orcid.org/0000-0003-2147-489X
Jane ApperleyCentre for Haematology, Imperial College NHS Trust, London, UK.ORCID http://orcid.org/0000-0002-1710-1794
Jiri MayerDepartment of Internal Medicine, Hematology and Oncology, University Hospital Brno and Masaryk University, Brno, Czech Republic.
Andreas HochhausKlinik für Innere Medizin II, Universitätsklinikum Jena, Jena, Germany.ORCID http://orcid.org/0000-0003-0626-0834
Markus PfirrmannInstitut für Medizinische Informationsverarbeitung, Biometrie und Epidemiologie (IBE), Medizinische Fakultät, Ludwig-Maximilians-Universität München, Munich, Germany.ORCID http://orcid.org/0000-0002-8948-0690
Annamaria BrioliKlinik für Innere Medizin II, Universitätsklinikum Jena, Jena, Germany. brioli.annamaria@mh-hannover.de.ORCID http://orcid.org/0000-0002-4072-7592

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Currently there is no established prognostic scoring system for patients with chronic myeloid leukemia (CML) in blast phase (BP). This study aimed to identify prognostic factors of CML-BP in a large cohort of prospectively and retrospectively collected patients and to develop a readily available prognostic scoring system at the onset of BP to enable future comparison between different trials and series. The analyses were based on 275 patients from thirteen countries, collected within the European LeukemiaNet Blast Phase Registry with a median observation time of 45 months and a median OS of 18.9 months. A Cox proportional hazards model for overall survival (OS) was employed, missing values were imputed. The study identified six independent prognostic factors: blast percentage, platelet count, age (all at onset of CML-BP), immunophenotype of BP, extramedullary disease, and previous history of CML. The low-risk group, encompassing 14% of patients, had a median OS of 97 months, the intermediate-risk group (59% of patients) of 22 months, and the high-risk group (27% of patients) of 9 months. Cross-validation demonstrated a good performance of the score, although external validation is strongly recommended. Despite the inherent limitations of registry data, the findings offer robust insights into prognostic factors for CML-BP.

Indexed as

Blast CrisisLeukemia, Myelogenous, Chronic, BCR-ABL PositiveAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedPrognosisProspective StudiesRegistriesRetrospective StudiesYoung Adult

Identifiers

PMID41714405
PMCPMC13056570

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