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

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Authors: Michael Lauseker, Tomasz Sacha, Hana Klamova, Julia Yakoleva, Elza Lomaia, Dragana Milojković, Christian Fabisch, Franck E. Nicolini, Ulla Olsson-Strömberg, Daniela Žáčková, Krzysztof Lewandowski, Philipp Ernst
+29 more Fausto Castagnetti, Klaus Hirschbühl, I Zupan, Astghik A. Voskanyan, Aleksandra Gołoś, Jochen J. Frietsch, Justyna Gil, Edgar Faber, Stefan W. Krause, Anne Parry, Susanne Saussele, Sonja Heibl, Georg-Nikolaus Franke, Luis Felipe Casado, Edyta Paczkowska, Holger Frithjof Hebart, Matthias Eder, Peter Anhut, Karolin Trautmann‐Grill, Elżbieta Szczepanek, Thomas Südhoff, Elżbieta Patkowska, Alexander Kiani, Thomas Ernst, Jane Apperley, Jiri Mayer, Andreas Hochhaus, Markus Pfirrmann, Annamaria Brioli
Cited by: 1
References: 20

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.

Fields of Study & Subjects

Chronic Myeloid Leukemia Treatments Acute Myeloid Leukemia Research Myeloproliferative Neoplasms: Diagnosis and Treatment

Publication details

Journal / source
Leukemia
Publisher
Springer Science and Business Media LLC
Volume
40
Issue
4
Pages
751–758
Publication date
19 February 2026
Language
EN