Stem cell transplantation with reduced-intensity conditioning for hemophagocytic lymphohistiocytosis

被引:139
作者
Cooper, N [1 ]
Rao, K [1 ]
Gilmour, K [1 ]
Hadad, L [1 ]
Adams, S [1 ]
Cale, C [1 ]
Davies, G [1 ]
Webb, D [1 ]
Veys, P [1 ]
Amrolia, P [1 ]
机构
[1] Great Ormond St Hosp Sick Children, London WC1N 3JH, England
关键词
D O I
10.1182/blood-2005-05-1819
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Allogeneic stem cell transplantation (SCT) is curative for hemophagocytic lympho-histiocytosis (HLH). However, patients frequently have significant morbidity before transplantation and there is high transplant-related mortality (TRM). Because first-degree HLH is caused by immune dysregulation, a reduced-intensity conditioned (RIC) regimen might be sufficient for cure while decreasing the TRM. Twelve patients with HLH underwent RIC SCT from a matched family/unrelated or haploidentical donor. Eleven were conditioned with fludarabine/melphalan with additional busulphan for haploidentical grafts. One received fludarabine and 2-Gy total body irradiation (TBI). All patients showed engraftment at a median of 14 days. Nine of 12 (75%) are alive and in complete remission (CR) a median of 30 months (range, 9-73 months) after SCT. Two patients died from pneumonitis and one from hepatic rupture. Four patients developed acute graft-versus-host disease (GVHD) and 3 have chronic GVHD. Three of 9 survivors have mixed chimerism but remain free of disease. In summary, RIC compares favorably to conventional SCT with long-term disease control in surviving patients despite a significant incidence of mixed chimerism.
引用
收藏
页码:1233 / 1236
页数:4
相关论文
共 18 条
[1]   Outcome for children after failed transplant for primary haemophagocytic lymphohistiocytosis [J].
Ardeshna, KM ;
Hollifield, J ;
Chessells, JM ;
Veys, P ;
Webb, DKH .
BRITISH JOURNAL OF HAEMATOLOGY, 2001, 115 (04) :949-952
[2]  
Arico M, 1996, LEUKEMIA, V10, P197
[3]   Hemophagocytic lymphohistiocytosis due to germline mutations in SH2D1A, the X-linked lymphoproliferative disease gene [J].
Arico, M ;
Imashuku, S ;
Clementi, R ;
Hibi, S ;
Teramura, T ;
Danesino, C ;
Haber, DA ;
Nichols, KE .
BLOOD, 2001, 97 (04) :1131-1133
[4]  
BLANCHE S, 1991, BLOOD, V78, P51
[5]   Characteristic immune abnormalities in hemophagocytic lymphohistiocytosis [J].
Egeler, RM ;
Shapiro, R ;
Loechelt, B ;
Filipovich, A .
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 1996, 18 (04) :340-345
[6]   NATURAL-KILLER CELL-FUNCTION AND INTERFERON-PRODUCTION IN FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS [J].
EIFE, R ;
JANKA, GE ;
BELOHRADSKY, BH ;
HOLTMANN, H .
PEDIATRIC HEMATOLOGY AND ONCOLOGY, 1989, 6 (03) :265-272
[7]   Sequence analysis of the granulysin and granzyme B genes in familial hemophagocytic lymphohistiocytosis [J].
Ericson, KG ;
Fadeel, B ;
Andersson, M ;
Gudmundsson, GH ;
Gürgey, A ;
Yalman, N ;
Janka, G ;
Nordenskjöld, M ;
Henter, JI .
HUMAN GENETICS, 2003, 112 (01) :98-99
[8]   Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis [J].
Ericson, KG ;
Fadeel, B ;
Nilsson-Ardnor, S ;
Söderhäll, C ;
Samuelsson, A ;
Janka, G ;
Schneider, M ;
Gürgey, A ;
Yalman, N ;
Révész, T ;
Egeler, RM ;
Jahnukainen, K ;
Storm-Mathiesen, I ;
Haraldsson, A ;
Poole, J ;
de Saint Basile, G ;
Nordenskjöld, M ;
Henter, JI .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (03) :590-597
[9]   Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3) [J].
Feldmann, J ;
Callebaut, I ;
Raposo, G ;
Certain, S ;
Bacq, D ;
Dumont, C ;
Lambert, N ;
Ouachée-Chardin, M ;
Chedeville, G ;
Tamary, H ;
Minard-Colin, V ;
Vilmer, E ;
Blanche, S ;
Le Deist, F ;
Fischer, A ;
Saint Basile, GD .
CELL, 2003, 115 (04) :461-473
[10]   Biology and treatment of familial hemophagocytic lymphohistiocytosis: Importance of perforin in lymphocyte-mediated cytotoxicity and triggering of apoptosis [J].
Henter, JI .
MEDICAL AND PEDIATRIC ONCOLOGY, 2002, 38 (05) :305-309