The effect of iron chelation on haemopoiesis in MDS patients with transfusional iron overload

被引:140
作者
Jensen, PD
Heickendorff, L
Pedersen, B
BendixHansen, K
Jensen, FT
Christensen, T
Boesen, AM
Ellegaard, J
机构
[1] AARHUS UNIV HOSP,AARHUS KOMMUNE HOSP,DEPT CLIN BIOCHEM,DK-8000 AARHUS C,DENMARK
[2] AARHUS UNIV HOSP,AARHUS KOMMUNE HOSP,DEPT CYTOGENET,DANISH CANC SOC,DK-8000 AARHUS C,DENMARK
[3] AARHUS UNIV HOSP,AARHUS KOMMUNE HOSP,INST PATHOL,DK-8000 AARHUS C,DENMARK
[4] AARHUS UNIV HOSP,SKEJBY SYGEHUS,CTR NUCL MAGNET RESONANCE,DK-8000 AARHUS C,DENMARK
关键词
iron overload; desferrioxamine; myelodysplastic syndromes; transferrin receptor;
D O I
10.1046/j.1365-2141.1996.d01-1795.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Long-term follow-up data are presented on changes in peripheral blood counts and Hb requirements of 11 patients with myelodysplastic syndromes (MDS) during iron chelation treatment with desferrioxamine for up to 60 months. The erythroid marrow activity was indirectly evaluated by repeated determinations of the serum transferrin receptor concentration. The efficacy of iron chelation was evaluated by repeated quantitative determination of the liver iron concentration by magnetic resonance imaging. Reduction in the Hb requirement (greater than or equal to 50%) was seen in 7/11 (64%) patients. Five patients (46%) became blood transfusion independent. Platelet counts increased in 7/11 (64%) patients and the neutrophil counts in 7/9 (78%) evaluable patients. All patients in whom iron chelation was highly effective showed improvement of erythropoietic output accompanied by an increase in the serum transferrin receptor concentration. It is concluded that reduction in cytopenia in MDS patients may be accomplished by treatment: with desferrioxamine, if the iron chelation is efficient and the patients are treated for a sufficiently long period of time, Exactly how treatment with desferrioxamine works remains a challenge for further investigation.
引用
收藏
页码:288 / 299
页数:12
相关论文
共 28 条
[1]   TRANSFERRIN RECEPTORS IN RAT PLASMA [J].
BEGUIN, Y ;
HUEBERS, HA ;
JOSEPHSON, B ;
FINCH, CA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (02) :637-640
[2]  
BEGUIN Y, 1993, BLOOD, V81, P1067
[3]   PROPOSALS FOR THE CLASSIFICATION OF THE MYELODYSPLASTIC SYNDROMES [J].
BENNETT, JM ;
CATOVSKY, D ;
DANIEL, MT ;
FLANDRIN, G ;
GALTON, DAG ;
GRALNICK, HR ;
SULTAN, C .
BRITISH JOURNAL OF HAEMATOLOGY, 1982, 51 (02) :189-199
[4]  
BOWEN DT, 1994, LEUKEMIA, V8, P151
[5]  
CAZZOLA M, 1988, BLOOD, V71, P305
[6]  
CAZZOLA M, 1992, BLOOD, V79, P29
[7]  
CHITAMBAR CR, 1991, BLOOD, V78, P2444
[8]  
CHUI DHK, 1982, BLOOD, V60, P362
[9]  
DEZZA L, 1989, LEUKEMIA, V3, P104
[10]  
ESTROV Z, 1987, BLOOD, V69, P757