Unrelated donor bone marrow transplantation for children with juvenile myelomonocytic leukaemia

被引:54
作者
Smith, FO
King, R
Nelson, G
Wagner, JE
Robertson, KA
Sanders, JE
Bunin, N
Emaunel, PD
Davis, SM
机构
[1] Childrens Hosp, Med Ctr, Div Hematol Oncol, Cincinnati, OH 45229 USA
[2] Univ Minnesota, Minneapolis, MN USA
[3] Natl Marrow Donor Program, Minneapolis, MN USA
[4] Indiana Univ, Sch Med, Hermann B Wells Ctr Pediat Res, Indianapolis, IN 46202 USA
[5] Indiana Univ, Sch Med, Dept Pediat, Sect Pediat Hematol Oncol, Indianapolis, IN 46202 USA
[6] Univ Washington, Sch Med, Dept Pediat, Seattle, WA 98195 USA
[7] Univ Washington, Sch Med, Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98195 USA
[8] Univ Washington, Sch Med, Dept Pediat, Seattle, WA 98195 USA
[9] Childrens Hosp Philadelphia, Div Oncol, Philadelphia, PA 19104 USA
[10] Univ Alabama Birmingham, Dept Med, Birmingham, AL 35294 USA
关键词
juvenile myelomonocytic leukaemia; bone marrow transplantation; National Marrow Donor Program; relapse; graft-versus-host disease;
D O I
10.1046/j.0007-1048.2001.03333.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Children with juvenile myelomonocytic leukaemia (JMML) have a poor outcome, with survival in a minority of patients. The major limitation on success of sibling donor bone marrow transplantation for JMML has been reported to be relapse. A total of 46 children with it diagnosis of JMML underwent unrelated donor marrow (URD) transplantation facilitated by the National Marrow Donor Program. Forty-three of 40 patients had neutrophil engraftment at a median of 20 d post transplant, with platelet recovery in 28 of 40 evaluable patients at a median of 34-5 d. Thirty-two of 44 evaluable patients developed acute graft-versus-host-disease (GVHD) (Grades 2-4) and chronic GVHD developed in 14 of 35 evaluable patients, At a median follow-up of 2.0 years. probabilities of survival and disease-free survival were 42% and 24'% respectively. The probability of relapse was 58% at 2 years and represents the major cause of treatment failure. Multivariate analysis revealed that chronic GVHD was associated with reduced relapse [risk ratio 0.20 (95% CI 0.04-1.02, P=0.05)] improved survival [risk ratio 0.13 (95% CI 0.03-0.68. P=0.02)] and event-free survival [risk ratio 0.23 (95% CI 0.06-0.94. P=0.04)]. This study demonstrates that relapse is the major cause of treatment failure in patients with JMML undergoing URD transplantation. With lower relapse observed in patients with chronic GVHD. new treatment strategies that focus on enhancing the graft-versus-leukaemia effect may improve survival.
引用
收藏
页码:716 / 724
页数:9
相关论文
共 64 条
[21]   Myelodysplasia and myeloproliferative disorders in childhood: An update [J].
Emanuel, PD .
BRITISH JOURNAL OF HAEMATOLOGY, 1999, 105 (04) :852-863
[22]   Inhibition of juvenile myelomonocytic leukemia cell growth in vitro by farnesyltransferase inhibitors [J].
Emanuel, PD ;
Snyder, RC ;
Wiley, T ;
Gopurala, B ;
Castleberry, RP .
BLOOD, 2000, 95 (02) :639-645
[23]   Juvenile myelomonocytic leukemia: Molecular understanding and prospects for therapy [J].
Emanuel, PD ;
Shannon, KM ;
Castleberry, RP .
MOLECULAR MEDICINE TODAY, 1996, 2 (11) :468-475
[24]  
EMANUEL PD, 1991, BLOOD, V77, P925
[25]  
ESTROV Z, 1987, BLOOD, V70, P1466
[26]   CHILDHOOD MONOSOMY-7 REVISITED [J].
EVANS, JPM ;
CZEPULKOWSKI, B ;
GIBBONS, B ;
SWANSBURY, GJ ;
CHESSELLS, JM .
BRITISH JOURNAL OF HAEMATOLOGY, 1988, 69 (01) :41-45
[27]   JUVENILE CHRONIC MYELOCYTIC-LEUKEMIA - EXPERIENCE WITH INTENSIVE COMBINATION CHEMOTHERAPY [J].
FESTA, RS ;
SHENDE, A ;
LANZKOWSKY, P .
MEDICAL AND PEDIATRIC ONCOLOGY, 1990, 18 (04) :311-316
[28]  
Frankel AE, 1998, BLOOD, V92, P4279
[29]  
FREEDMAN MH, 1988, AM J PEDIAT HEMATOL, V10, P261
[30]   FARNESYLTRANSFERASE INHIBITORS - RAS RESEARCH YIELDS A POTENTIAL CANCER THERAPEUTIC [J].
GIBBS, JB ;
OLIFF, A ;
KOHL, NE .
CELL, 1994, 77 (02) :175-178