Autografting as a risk factor for persisting iron overload in long-term survivors of acute myeloid leukaemia

被引:26
作者
Butt, NM [1 ]
Clark, RE [1 ]
机构
[1] Royal Liverpool Univ Hosp, Dept Haematol, Liverpool L7 8XP, Merseyside, England
关键词
iron overload; acute myeloid leukaemia; autograft; ferritin;
D O I
10.1038/sj.bmt.1704244
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We studied the iron status of 32 evaluable adult acute myeloid leukaemia (AML) survivors who were entered into the UK Medical Research Council acute myeloid leukaemia (AML) 10 and 12 trials at our institution between 1988 and 1998. Patients were required to have been independent of all blood products for at least 3 years. As a group, the median first serum ferritin level was 1323 mug/l (NR 19-300 mug/l) at a median of 1321 days from the last transfusion confirming the presence of significant iron overload persisting for some years after completion of all therapy and blood products. There was a general trend for the serum ferritin level to fall with time, but the fall was less pronounced in men and carriers of the C282Y mutation. Recipients of autologous stem cell transplantation (SCT) had a higher median first serum ferritin level (3245 mug/l) than patients who received chemotherapy alone (1148 mug/l) or allogeneic SCT (1334 mug/l) because of increased use of transfused blood. Nine of the 10 recipients of autologous SCT underwent venesection. No evidence of end organ damage was seen in any patient. Serial monitoring of serum ferritin and assessment of the C282Y status may be useful in all long-term AML survivors, especially autograft recipients.
引用
收藏
页码:909 / 913
页数:5
相关论文
共 18 条
[1]  
Beutler E, 1997, AM J HUM GENET, V61, P762
[2]   Randomised comparison of addition of autologous bone-marrow transplantation to intensive chemotherapy for acute myeloid leukaemia in first remission: results of MRC AML 10 trial [J].
Burnett, AK ;
Goldstone, AH ;
Stevens, RMF ;
Hann, IM ;
Rees, JKH ;
Gray, RG ;
Wheatley, K .
LANCET, 1998, 351 (9104) :700-708
[3]   EFFECT OF ASCORBIC-ACID DEFICIENCY ON SERUM FERRITIN CONCENTRATION IN PATIENTS WITH BETA-THALASSEMIA MAJOR AND IRON OVERLOAD [J].
CHAPMAN, RWG ;
HUSSAIN, MAM ;
GORMAN, A ;
LAULICHT, M ;
POLITIS, D ;
FLYNN, DM ;
SHERLOCK, S ;
HOFFBRAND, AV .
JOURNAL OF CLINICAL PATHOLOGY, 1982, 35 (05) :487-491
[4]   Hemochromatosis gene in leukemia and lymphoma [J].
Dorak, MT ;
Burnett, AK ;
Worwood, M .
LEUKEMIA & LYMPHOMA, 2002, 43 (03) :467-477
[5]   A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis [J].
Feder, JN ;
Gnirke, A ;
Thomas, W ;
Tsuchihashi, Z ;
Ruddy, DA ;
Basava, A ;
Dormishian, F ;
Domingo, R ;
Ellis, MC ;
Fullan, A ;
Hinton, LM ;
Jones, NL ;
Kimmel, BE ;
Kronmal, GS ;
Lauer, P ;
Lee, VK ;
Loeb, DB ;
Mapa, FA ;
McClelland, E ;
Meyer, NC ;
Mintier, GA ;
Moeller, N ;
Moore, T ;
Morikang, E ;
Prass, CE ;
Quintana, L ;
Starnes, SM ;
Schatzman, RC ;
Brunke, KJ ;
Drayna, DT ;
Risch, NJ ;
Bacon, BR ;
Wolff, RK .
NATURE GENETICS, 1996, 13 (04) :399-408
[6]  
GABUTTI V, 1994, BAIL CL HAE, V7, P919, DOI 10.1016/S0950-3536(05)80131-3
[7]  
Hannuksela J, 2002, HAEMATOLOGICA, V87, P131
[8]   Role of non-transferrin bound iron in iron overload and liver dysfunction in long term survivors of acute leukaemia and bone marrow transplantation [J].
Harrison, P ;
Neilson, JR ;
Marwah, SS ;
Madden, L ;
Bareford, D ;
Milligan, DW .
JOURNAL OF CLINICAL PATHOLOGY, 1996, 49 (10) :853-856
[9]  
Hollan S R, 1997, Curr Opin Hematol, V4, P436
[10]  
KONIJN AM, 1977, BRIT J HAEMATOL, V37, P7, DOI 10.1111/j.1365-2141.1977.tb08758.x