Incidence of blast phase in myelofibrosis according to anemia severity.
acute myeloid leukemia
essential thrombocythemia
myelofibrosis
polycythemia vera
ruxolitinib
Journal
EJHaem
ISSN: 2688-6146
Titre abrégé: EJHaem
Pays: United States
ID NLM: 101761942
Informations de publication
Date de publication:
Aug 2023
Aug 2023
Historique:
received:
21
05
2023
revised:
06
06
2023
accepted:
15
06
2023
medline:
21
8
2023
pubmed:
21
8
2023
entrez:
21
8
2023
Statut:
epublish
Résumé
Myelofibrosis (MF) is a clonal malignancy frequently characterized by anemia and in 10%-20% of cases it can evolve into blast phase (BP). Anemia in MF is associated with reduced survival and -in primary MF- also with an increased probability of BP. Conventional treatments for anemia have limited effectiveness in MF. Within a dataset of 1752 MF subjects largely unexposed to ruxolitinib (RUX), BP incidence was 2.5% patients per year (p-y). This rate reached respectively 4.3% and 4.5% p-y in case of patients with common terminology criteria for adverse events (CTCAE) grade 3/4 and grade 2 anemia, respectively, that represented together 32% of the cohort. Among 273 MF cases treated with RUX, BP incidence was 2.89% p-y and it reached 4.86% p-y in subjects who started RUX with CTCAE grade 2 anemia (one third of total). Within patients with red blood cell transfusion-dependency at 6 months of RUX (21% of the exposed), BP rate was 4.2% p-y. Our study highlights a relevant incidence of BP in anemic MF patients, with a similar rate whether treated with or without RUX. These findings will help treating physicians to make decisions on the safety profile of innovative anemia treatments.
Identifiants
pubmed: 37601878
doi: 10.1002/jha2.745
pii: JHA2745
pmc: PMC10435699
doi:
Types de publication
Journal Article
Langues
eng
Pagination
679-689Informations de copyright
© 2023 The Authors. eJHaem published by British Society for Haematology and John Wiley & Sons Ltd.
Déclaration de conflit d'intérêts
BM received honoraria for lecture from Novartis. FP received honoraria for lectures and advisory boards from Novartis, GSK, Bristol‐Myers Squibb/Celgene, Sierra Oncology, Abbvie, Janssen, Roche, AOP Orphan, Karyiopharma, Kyowa Kirin and MEI, Sumitomo. Other authors have no conflict of interest to disclose.
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