Literature DB >> 29477023

Iron overload in lower international prognostic scoring system risk patients with myelodysplastic syndrome receiving red blood cell transfusions: Relation to infections and possible benefit of iron chelation therapy.

Colleen A C Wong1, Shannon A Y Wong1, Heather A Leitch2.   

Abstract

BACKGROUND: An increased incidence of infections and infectious mortality has been reported in myelodysplastic syndromes (MDS) patients receiving red blood cell (RBC) transfusions.
METHODS: We examined incidence of infections requiring antibiotics, antifungal or antiviral medications in transfused lower International Prognostic Scoring System (IPSS) risk MDS patients and whether this differed with iron chelation therapy (ICT).
RESULTS: 138 transfused MDS patients were lower IPSS risk. 59 received ICT; median duration was 13 months. There was no significant difference between groups in neutrophil count at first RBC transfusion or first infection. Infections included: bacterial, n = 88; viral; fungal; and mycobacterial; n = 2 each. In ICT and non-ICT patients, respectively, infections were (number [%]): patients, 23 (40.0%) and 22 (27.8%); episodes (median [range]), 2 (1-6) and 2 (1-5); hospitalizations, 16 (27.1%) and 8 (10.1%); and deaths, 0 (0%) and 1 (1.3%), p = NS for all. Median overall survival (OS) from first RBC transfusion was superior in ICT patients, p = 0.01, and remained significant in a multivariate analysis (MVA), p = 0.003. Median time to first infection (TTI) was 27 and 7.8 months, respectively, p < 0.0001, and ICT remained significant for TTI in an MVA, p = 0.02, hazard ratio 0.3. For ICT patients with blast count <5%, TTI was significantly superior (p = 0.004).
CONCLUSIONS: In this retrospective analysis, for lower IPSS risk MDS patients receiving RBC transfusions, though number and type of infections were similar between groups and despite similar neutrophil counts, time to first infection was significantly longer in ICT patients (p < 0.0001). These results should be confirmed in larger, prospective analyses.
Copyright © 2018 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Infection; Iron chelation therapy; Iron overload; MDS

Mesh:

Substances:

Year:  2018        PMID: 29477023     DOI: 10.1016/j.leukres.2018.02.005

Source DB:  PubMed          Journal:  Leuk Res        ISSN: 0145-2126            Impact factor:   3.156


  5 in total

Review 1.  Controversies on the Consequences of Iron Overload and Chelation in MDS.

Authors:  Francesca Vinchi; Saskia Hell; Uwe Platzbecker
Journal:  Hemasphere       Date:  2020-05-27

2.  Iron Overload Mimicking Conditions Skews Bone Marrow Dendritic Cells Differentiation into MHCIIlowCD11c+CD11b+F4/80+ Cells.

Authors:  Giulio Verna; Marina Liso; Stefania De Santis; Manuela Dicarlo; Elisabetta Cavalcanti; Alberto Crovace; Annamaria Sila; Pietro Campiglia; Angelo Santino; Antonio Lippolis; Grazia Serino; Alessio Fasano; Marcello Chieppa
Journal:  Int J Mol Sci       Date:  2020-02-17       Impact factor: 5.923

3.  Modulation of the Immune Response by Deferasirox in Myelodysplastic Syndrome Patients.

Authors:  Hana Votavova; Zuzana Urbanova; David Kundrat; Michaela Dostalova Merkerova; Martin Vostry; Monika Hruba; Jaroslav Cermak; Monika Belickova
Journal:  Pharmaceuticals (Basel)       Date:  2021-01-07

Review 4.  Infections in Myelodysplastic Syndrome in Relation to Stage and Therapy.

Authors:  Giuseppe Leone; Livio Pagano
Journal:  Mediterr J Hematol Infect Dis       Date:  2018-07-01       Impact factor: 3.122

5.  Iron overload impairs normal hematopoietic stem and progenitor cells through reactive oxygen species and shortens survival in myelodysplastic syndrome mice.

Authors:  Xin Jin; Xiaoyuan He; Xiaoli Cao; Ping Xu; Yi Xing; Songnan Sui; Luqiao Wang; Juanxia Meng; Wenyi Lu; Rui Cui; Hongyan Ni; Mingfeng Zhao
Journal:  Haematologica       Date:  2018-06-14       Impact factor: 9.941

  5 in total

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