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Real-world study of tagraxofusp monotherapy in relapsed or refractory blastic plasmacytoid dendritic cell neoplasm

  • Patients with relapsed/refractory blastic plasmacytoid dendritic cell neoplasm (BPDCN) have limited treatment options. Tagraxofusp is the only drug approved for BPDCN. To provide real-world data on tagraxofusp in clinical practice, we report an analysis of safety and efficacy in adults who obtained tagraxofusp via a European named-patient program. Twenty-four patients (median age 68 years) with relapsed/refractory BPDCN received tagraxofusp 12 μg/kg intravenously days 1–5 of a 21-day cycle. Twenty patients (efficacy-evaluable) had a 65% overall response rate (ORR), 9.5-month median duration of response, 3.6-month median progression-free survival, and 8.4-month median overall survival (OS). Ten patients bridged to HSCT with a median OS not reached. There were no new safety signals. Capillary leak syndrome was manageable, mostly occurring during cycle one. These results support tagraxofusp for relapsed/refractory BPDCN after prior chemotherapy. Furthermore, the high transplant ratePatients with relapsed/refractory blastic plasmacytoid dendritic cell neoplasm (BPDCN) have limited treatment options. Tagraxofusp is the only drug approved for BPDCN. To provide real-world data on tagraxofusp in clinical practice, we report an analysis of safety and efficacy in adults who obtained tagraxofusp via a European named-patient program. Twenty-four patients (median age 68 years) with relapsed/refractory BPDCN received tagraxofusp 12 μg/kg intravenously days 1–5 of a 21-day cycle. Twenty patients (efficacy-evaluable) had a 65% overall response rate (ORR), 9.5-month median duration of response, 3.6-month median progression-free survival, and 8.4-month median overall survival (OS). Ten patients bridged to HSCT with a median OS not reached. There were no new safety signals. Capillary leak syndrome was manageable, mostly occurring during cycle one. These results support tagraxofusp for relapsed/refractory BPDCN after prior chemotherapy. Furthermore, the high transplant rate suggests tagraxofusp offers an opportunity for bridge to transplant in this difficult-to-treat population.show moreshow less

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Metadaten
Author:Emanuele Angelucci, Eric Deconinck, Tobias Matthieu Benoit, Krischan Braitsch, Cristina Papayannidis, Ann-Kristin SchmaelterGND, Dimoula Erakli, Michael Zuurman, Marco Herling
Frontdoor URLhttps://opus.bibliothek.uni-augsburg.de/opus4/125471
ISSN:1042-8194OPAC
ISSN:1029-2403OPAC
Parent Title (English):Leukemia & Lymphoma
Publisher:Informa UK
Place of publication:London
Type:Article
Language:English
Year of first Publication:2025
Publishing Institution:Universität Augsburg
Release Date:2025/09/24
DOI:https://doi.org/10.1080/10428194.2025.2553862
Institutes:Medizinische Fakultät
Medizinische Fakultät / Universitätsklinikum
Medizinische Fakultät / Lehrstuhl für Innere Medizin mit Schwerpunkt Hämatologie und Onkologie
Dewey Decimal Classification:6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Latest Publications (not yet published in print):Aktuelle Publikationen (noch nicht gedruckt erschienen)
Licence (German):CC-BY 4.0: Creative Commons: Namensnennung (mit Print on Demand)