Literature DB >> 24333115

Transfusion dependence development and disease evolution in patients with MDS and del(5q) and without transfusion needs at diagnosis.

Silvia M Rojas1, María Díez-Campelo2, Elisa Luño3, Mónica Cabrero1, Carme Pedro4, Marisa Calabuig5, Benet Nomdedeu6, Teresa Cedena7, Beatriz Arrizabalaga8, Marta García9, Carlos Cerveró10, Rosa Collado11, Gemma Azaceta12, M Teresa Ardanaz13, Juan Antonio Muñoz14, Blanca Xicoy15, M José Requena Rodríguez16, Joan Bargay17, M Jesús Arilla Morell18, Adriana Simiele19, Consuelo del Cañizo1.   

Abstract

Patients with isolated del(5q) and MDS are considered to have good prognosis as compared to other MDS subtypes. Most patients suffered of anemia and 50% of them required transfusions at diagnosis. It is known that for patients with MDS and del(5q) in transfusion dependence(TD), Lenalidomide is the first choice treatment. However, there are no data regarding natural evolution of anemia in patients diagnosed in MDS and del(5q) without TD, factors that may impact on the development of TD or disease outcome. In the present study we have performed a retrospective multicenter analysis on 83 patients with low-int 1 MDS and del(5q) without TD. During the study 61 patients became TD at a median of 1.7 years and only the Hb level 9 g/dL was associated with poorer TFS (p = 0.007) in the multivariate analysis. Among these 61 TD patients, 49 received treatment (19 Lenalidomide). Median follow up was 48 months, estimated OS at 2 and 5 year was 92% and 50% respectively. In the multivariate analysis for OS, platelets <100,000 mm(-3) and Lenalidomide treatment retained the statistical significant impact. LFS at 2 and 5 years was 86% and 73% respectively, and median time to sAML was 8.16 years (CI 95%: 6.05-10.27). In the multivariate analysis only thrombocytopenia retained statistical significance. In summary, this retrospective study show that level of Hb is an important parameter in order to determine the time until TD, it should be also stressed the importance of an early treatment in order to prevent TD development and shorter survival.
Copyright © 2013 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Hb level; Myelodysplastic syndrome; Survival; Transfusion dependence; del(5q)

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Year:  2013        PMID: 24333115     DOI: 10.1016/j.leukres.2013.11.005

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


  2 in total

1.  ROS-mediated iron overload injures the hematopoiesis of bone marrow by damaging hematopoietic stem/progenitor cells in mice.

Authors:  Xiao Chai; Deguan Li; Xiaoli Cao; Yuchen Zhang; Juan Mu; Wenyi Lu; Xia Xiao; Chengcheng Li; Juanxia Meng; Jie Chen; Qing Li; Jishi Wang; Aimin Meng; Mingfeng Zhao
Journal:  Sci Rep       Date:  2015-05-13       Impact factor: 4.379

2.  Part 4: Myelodysplastic syndromes-Treatment of low-risk patients with the 5q deletion.

Authors:  Silvia Maria Meira Magalhães; Elvira Deolinda Rodrigues Pereira Velloso; Renata Buzzini; Wanderley Marques Bernardo
Journal:  Hematol Transfus Cell Ther       Date:  2018-07-27
  2 in total

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