Allogeneic hematopoietic cell transplantation for XIAP deficiency: an international survey reveals poor outcomes

被引:117
作者
Marsh, Rebecca A. [1 ]
Rao, Kanchan [2 ]
Satwani, Prakash [3 ]
Lehmberg, Kai [4 ]
Mueller, Ingo [4 ]
Li, Dandan [5 ]
Kim, Mi-Ok [5 ]
Fischer, Alain [6 ]
Latour, Sylvain [7 ]
Sedlacek, Petr [8 ]
Barlogis, Vincent [9 ]
Hamamoto, Kazuko [10 ]
Kanegane, Hirokazu [11 ]
Milanovich, Sam [12 ]
Margolis, David A. [12 ]
Dimmock, David [13 ]
Casper, James [12 ]
Douglas, Dorothea N. [14 ]
Amrolia, Persis J. [2 ]
Veys, Paul [2 ]
Kumar, Ashish R. [1 ]
Jordan, Michael B. [1 ]
Bleesing, Jack J. [1 ]
Filipovich, Alexandra H. [1 ]
机构
[1] Cincinnati Childrens Hosp Med Ctr, Div Bone Marrow Transplantat & Immunodeficiency, Cincinnati, OH 45229 USA
[2] Great Ormond St Hosp Sick Children, Dept Haematol & Bone Marrow Transplantat, London, England
[3] Columbia Univ, Med Ctr, Morgan Stanley Childrens Hosp New York Presbyteri, Div Pediat Blood & Marrow Transplantat, New York, NY USA
[4] Univ Med Ctr Hamburg Eppendorf, Clin Pediat Hematol & Oncol, Hamburg, Germany
[5] Cincinnati Childrens Hosp Med Ctr, Div Biostat & Epidemiol, Cincinnati, OH 45229 USA
[6] Univ Paris 05, Hop Necker, AP HP, INSERM,U768,Unite Immunol & Hematol,Inst Imagine, Paris, France
[7] Univ Paris 05, Hop Necker, INSERM, Inst Imagine,U768, Paris, France
[8] Charles Univ Prague, Univ Hosp Motol, Dept Pediat Hematol & Oncol, Prague, Czech Republic
[9] Hop Timone Enfants, Marseille, France
[10] Hiroshima Red Cross Hosp, Dept Pediat, Hiroshima, Japan
[11] Toyama Univ, Grad Sch Med, Dept Pediat, Toyama, Japan
[12] Childrens Hosp Wisconsin, Med Coll Wisconsin, Div Pediat Hematol Oncol & Bone Marrow Transplant, Milwaukee, WI 53201 USA
[13] Med Coll Wisconsin, Dept Pediat, Div Genet, Milwaukee, WI 53226 USA
[14] Arizona State Univ W, Coll Med, Phoenix Childrens Hosp, Phoenix, AZ 85069 USA
关键词
LINKED LYMPHOPROLIFERATIVE SYNDROME; FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; DISEASE; MANIFESTATIONS; APOPTOSIS; SURVIVAL; JAPAN; MICE; SAP;
D O I
10.1182/blood-2012-06-432500
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
There have been no studies on patient outcome after allogeneic hematopoietic cell transplantation (HCT) in patients with X-linked inhibitor of apoptosis (XIAP) deficiency. To estimate the success of HCT, we conducted an international survey of transplantation outcomes. Data were reported for 19 patients. Seven patients received busulfan-containing myeloablative conditioning (MAC) regimens. Eleven patients underwent reduced intensity conditioning (RIC) regimens predominantly consisting of alemtuzumab, fludarabine, and melphalan. One patient received an intermediate-intensity regimen. Survival was poor in the MAC group, with only 1 patient surviving (14%). Most deaths were from transplantation-related toxicities, including venoocclusive disease and pulmonary hemorrhage. Of the 11 patients who received RIC, 6 are currently surviving at a median of 570 days after HCT (55%). Preparative regimen and HLH activity affected outcomes, and of RIC patients reported to be in remission from HLH, survival is 86% (P = .03). We conclude that MAC regimens should not be used for patients with XIAP deficiency. It is possible that the loss of XIAP and its antiapoptotic functions contributes to the high incidence of toxicities observed with MAC regimens. RIC regimens should be pursued with caution and, if possible, efforts should be made to ensure HLH remission before HCT in these patients. (Blood. 2013;121(6):877-883)
引用
收藏
页码:877 / 883
页数:7
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