Myelodysplastic syndrome and acute myelogenous leukemia as a late clonal complication in children with acquired aplastic anemia

被引:141
作者
Ohara, A [1 ]
Kojima, S [1 ]
Hamajima, N [1 ]
Tsuchida, M [1 ]
Imashuku, S [1 ]
Ohta, S [1 ]
Sasaki, H [1 ]
Okamura, J [1 ]
Sugita, K [1 ]
Kigasawa, H [1 ]
Kiriyama, Y [1 ]
Akatsuka, J [1 ]
Tsukimoto, I [1 ]
机构
[1] JAPANESE SOC PEDIAT HEMATOL,APLAST ANEMIA COMM,TOKYO,JAPAN
关键词
D O I
10.1182/blood.V90.3.1009.1009_1009_1013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The improved outcome of acquired aplastic anemia (AA) has revealed later complications, such as myelodysplastic syndrome (MDS) and acute myelogenous leukemia (AML). We retrospectively analyzed 167 children with severe acquired AA, Eleven of 50 children treated with cyclosporin (CSA) and recombinant human granulocyte colony-stimulating factor (rhG-CSF) developed MDS/AML; 8 of these were within 36 months of the diagnosis of AA, much earlier than previous reports. Six of the 11 children received rhG-CSF exceeding 10 mu g/kg/d, and 9 received rhG-CSF therapy for over 1 year, Ten children showed monosomy 7 at diagnosis of MDS, All of the 11 children were administered both CSA and rhG-CSF. There was no development of MDS/AML among 41 children treated with either CSA or rhG-CSF or among 48 children who underwent bone marrow transplantation. A well-controlled clinical trial is warranted to determine whether therapeutic modalities affect the development of MDS/AML in children with severe acquired AA. (C) 1997 by The American Society of Hematology.
引用
收藏
页码:1009 / 1013
页数:5
相关论文
共 26 条
[1]   PANCYTOPENIA AS A CLONAL DISORDER OF A MULTIPOTENT HEMATOPOIETIC STEM-CELL [J].
ABKOWITZ, JL ;
FIALKOW, PJ ;
NIEBRUGGE, DJ ;
RASKIND, WH ;
ADAMSON, JW .
JOURNAL OF CLINICAL INVESTIGATION, 1984, 73 (01) :258-261
[2]  
[Anonymous], BLOOD
[3]  
APPELBAUM FR, 1987, EXP HEMATOL, V15, P1134
[4]   TREATMENT OF APLASTIC-ANEMIA (AA) WITH ANTILYMPHOCYTE GLOBULIN (ALG) AND METHYLPREDNISOLONE (MPRED) WITH OR WITHOUT ANDROGENS - A RANDOMIZED TRIAL FROM THE EBMT-SAA WORKING PARTY [J].
BACIGALUPO, A ;
CHAPLE, M ;
HOWS, J ;
VANLINT, MT ;
MCCANN, S ;
MILLIGAN, D ;
CHESSELLS, J ;
GOLDSTONE, AH ;
OTTOLANDER, J ;
VANTVEER, ET ;
COMOTTI, B ;
COSER, P ;
BROCCIA, G ;
BOSI, A ;
LOCASCIULLI, A ;
CATALANO, L ;
BATTISTA, R ;
ARCESE, W ;
CAROTENUTO, M ;
MARMONT, AM ;
SMITH, ECG .
BRITISH JOURNAL OF HAEMATOLOGY, 1993, 83 (01) :145-151
[5]   ANTILYMPHOCYTE GLOBULIN, CYCLOSPORINE, AND GRANULOCYTE-COLONY-STIMULATING FACTOR IN PATIENTS WITH ACQUIRED SEVERE APLASTIC-ANEMIA (SAA) - A PILOT-STUDY OF THE EBMT SAA WORKING PARTY [J].
BACIGALUPO, A ;
BROCCIA, G ;
CORDA, G ;
ARCESE, W ;
CAROTENUTO, M ;
GALLAMINI, A ;
LOCATELLI, F ;
MORI, PG ;
SARACCO, P ;
TODESCHINI, G ;
COSER, P ;
IACOPINO, P ;
VANLINT, MT ;
GLUCKMAN, E .
BLOOD, 1995, 85 (05) :1348-1353
[6]   BONE-MARROW TRANSPLANTATION (BMT) VERSUS IMMUNOSUPPRESSION FOR THE TREATMENT OF SEVERE APLASTIC-ANEMIA (SAA) - A REPORT OF THE EBMT SAA WORKING PARTY [J].
BACIGALUPO, A ;
HOWS, J ;
GLUCKMAN, E ;
NISSEN, C ;
MARSH, J ;
VANLINT, MT ;
CONGIU, M ;
DEPLANQUE, MM ;
ERNST, P ;
MCCANN, S ;
RAGAVASHAR, A ;
FRICKHOFEN, N ;
WURSCH, A ;
MARMONT, AM ;
GORDONSMITH, EC .
BRITISH JOURNAL OF HAEMATOLOGY, 1988, 70 (02) :177-182
[7]  
CAMITTA BM, 1979, BLOOD, V53, P504
[8]  
DALE D, 1994, BLOOD, V84, pA518
[9]  
DEPLANQUE MM, 1988, BRIT J HAEMATOL, V70, P55
[10]  
DEPLANQUE MM, 1989, BRIT J HAEMATOL, V73, P121