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Deferasirox in the management of iron overload in patients with myelofibrosis treated with ruxolitinib: The multicentre retrospective RUX-IOL study.

Authors :
Elli EM
Di Veroli A
Bartoletti D
Iurlo A
Carmosino I
Benevolo G
Abruzzese E
Bonifacio M
Bergamaschi M
Polverelli N
Caramella M
Cilloni D
Tiribelli M
Pugliese N
Caocci G
Crisà E
Porrini R
Markovic U
Renso R
Auteri G
Cattaneo D
Trawinska MM
Scaffidi L
Biale L
Bucelli C
Breccia M
Gambacorti-Passerini C
Palumbo GA
Latagliata R
Palandri F
Source :
British journal of haematology [Br J Haematol] 2022 Apr; Vol. 197 (2), pp. 190-200. Date of Electronic Publication: 2022 Feb 08.
Publication Year :
2022

Abstract

Deferasirox (DFX) is used for the management of iron overload (IOL) in many haematological malignancies including myelofibrosis (MF). The 'RUX-IOL' study retrospectively collected 69 MF patients treated with ruxolitinib (RUX) and DFX for IOL to assess: safety, efficacy in term of iron chelation response (ICR) and erythroid response (ER), and impact on overall survival of the combination therapy. The RUX-DFX therapy was administered for a median time of 12.4 months (interquartile range 3.1-71.2). During treatment, 36 (52.2%) and 34 (49.3%) patients required RUX and DFX dose reductions, while eight (11.6%) and nine (13.1%) patients discontinued due to RUX- or DFX-related adverse events; no unexpected toxicity was reported. ICR and ER were achieved by 33 (47.8%) and 32 patients (46.4%) respectively. Thirteen (18.9%) patients became transfusion-independent. Median time to ICR and ER was 6.2 and 2 months respectively. Patients achieving an ER were more likely to obtain an ICR also (p = 0.04). In multivariable analysis, the absence of leukocytosis at baseline (p = 0.02) and achievement of an ICR at any time (p = 0.02) predicted improved survival. In many MF patients, the RUX-DFX combination provided ICR and ER responses that correlated with improved outcome in the absence of unexpected toxicities. This strategy deserves further clinical investigation.<br /> (© 2022 British Society for Haematology and John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1365-2141
Volume :
197
Issue :
2
Database :
MEDLINE
Journal :
British journal of haematology
Publication Type :
Academic Journal
Accession number :
35137397
Full Text :
https://doi.org/10.1111/bjh.18057