Iron overload and chelation therapy in myelodysplastic syndromes

被引:41
|
作者
Temraz, Sally [1 ]
Santini, Valeria [2 ]
Musallam, Khaled [1 ]
Taher, Ali [1 ]
机构
[1] AUBMC, Dept Internal Med, Div Hematol Oncol, Beirut, Lebanon
[2] Univ Florence, AOU Careggi, Div Hematol, Florence, Italy
关键词
MDS; Myelodysplastic syndrome; Iron chelation; Iron overload; Transfusion-dependent; Deferasirox; Deferoxamine; Deferiprone; TRANSFUSION-DEPENDENT PATIENTS; BETA-THALASSEMIC MICE; LABILE PLASMA IRON; QUALITY-OF-LIFE; MDS PATIENTS; T2-ASTERISK-MAGNETIC RESONANCE; MULTICENTER TRIAL; IMPROVED SURVIVAL; HEMOGLOBIN LEVEL; UNITED-STATES;
D O I
10.1016/j.critrevonc.2014.01.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Iron overload remains a concern in MDS patients especially those requiring recurrent blood transfusions. The consequence of iron overload may be more relevant in patients with low and intermediate-1 risk MDS who may survive long enough to experience such manifestations. It is a matter of debate whether this overload has time to yield organ damage, but it is quite evident that cellular damage and DNA genotoxic effect are induced. Iron overload may play a critical role in exacerbating pre-existing morbidity or even unmask silent ones. Under these circumstances, iron chelation therapy could play an integral role in the management of these patients. This review entails an in depth analysis of iron overload in MDS patients; its pathophysiology, effect on survival, associated risks and diagnostic options. It also discusses management options in relation to chelation therapy used in MDS patients and the impact it has on survival, hematologic response and organ function. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:64 / 73
页数:10
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