Transplant-associated microangiopathy (TAM) in recipients of allogeneic hematopoietic stem cell transplants

被引:74
作者
Martinez, MT [1 ]
Bucher, C [1 ]
Stussi, G [1 ]
Heim, D [1 ]
Buser, A [1 ]
Tsakiris, DA [1 ]
Tichelli, A [1 ]
Gratwohl, A [1 ]
Passweg, JR [1 ]
机构
[1] Univ Basel Hosp, Div Hematol, CH-4031 Basel, Switzerland
关键词
transplant-associated microangiopathy; hemolytic uremic syndrome; thrombotic thrombopenic purpura; graft-versus-host disease; schistocytes;
D O I
10.1038/sj.bmt.1705160
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We studied occurrence, risk factors and outcome of patients with transplant-associated microangiopathy (TAM) after allogeneic stem cell transplantation (HSCT). A total of 221 consecutive patients were transplanted between 1995 and 2002. TAM is defined as evidence of hemolysis and schistocytes in the first 100 days. Outcomes analyzed included TAM and overall survival. Of 221 patients, 68 had TAM. The cumulative incidence was 31 ( 25 - 38)% at 100 days. Patients with TAM had higher LDH, higher bilirubin, higher creatinine and more often neurologic symptoms. TAM was not associated with stem cell source, cyclosporine levels and was not more frequent in recent years. In multivariate analysis, risk factors for TAM included donor type, age, gender, ABO-incompatibility and acute graft-versus-host disease (aGvHD). In patients with TAM, 1-year survival was lower than in patients without TAM (27 +/- 18% for TAM with high schistocyte counts; 53 +/- 15% for TAM with low schistocyte counts; vs 78 +/- 7% in patients without TAM; P<0.0001). TAM was independently associated with mortality adjusting for donor type, age and aGvHD occurrence and severity. TAM is frequent after HSCT and is associated with mortality even after adjustment for aGvHD grade. Risk factors of TAM are similar to aGvHD. TAM may represent endothelial damage driven by donor - host interactions.
引用
收藏
页码:993 / 1000
页数:8
相关论文
共 43 条
[1]   Endothelial injury mediated by cytotoxic T lymphocytes and loss of microvessels in chronic graft versus host disease [J].
Biedermann, BC ;
Sahner, S ;
Gregor, M ;
Tsakiris, DA ;
Jeanneret, C ;
Pober, JS ;
Gratwohl, A .
LANCET, 2002, 359 (9323) :2078-2083
[2]  
CARLSON K, 1993, BONE MARROW TRANSPL, V11, P205
[3]  
Champlin RE, 2000, BLOOD, V95, P3702
[4]  
CHAPPELL ME, 1988, BONE MARROW TRANSPL, V3, P339
[5]   Fatal thrombotic thrombocytopenic purpura as a rare complication following allogeneic stem cell transplantation [J].
Chemnitz, J ;
Fuchs, M ;
Blau, W ;
Hartmann, P ;
Wickenhauser, C ;
Scheid, C ;
Schulz, A ;
Diehl, V ;
Söhngen, D .
ANNALS OF HEMATOLOGY, 2000, 79 (09) :527-529
[6]   Sirolimus and tacrolimus without methotrexate as graft-versus-host disease prophylaxis after matched related donor peripheral blood stem cell transplantation [J].
Cutler, C ;
Kim, HT ;
Hochberg, E ;
Ho, V ;
Alyea, E ;
Lee, SJ ;
Fisher, DC ;
Miklos, D ;
Levin, J ;
Sonis, S ;
Soiffer, RJ ;
Antin, JH .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2004, 10 (05) :328-336
[7]   Transplantation-associated thrombotic microangiopathy: twenty-two years later [J].
Daly, AS ;
Xenocostas, A ;
Lipton, JH .
BONE MARROW TRANSPLANTATION, 2002, 30 (11) :709-715
[8]   Transplantation-associated thrombotic microangiopathy is associated with transplantation from unrelated donors, acute graft-versus-host disease and venoocclusive disease of the liver [J].
Daly, AS ;
Hasegawa, WS ;
Lipton, JH ;
Messner, HA ;
Kiss, TL .
TRANSFUSION AND APHERESIS SCIENCE, 2002, 27 (01) :3-12
[9]   Circulating endothelial cells: Realities and promises in vascular disorders [J].
Dignat-George, F ;
Sampol, J ;
Lip, G ;
Blann, AD .
PATHOPHYSIOLOGY OF HAEMOSTASIS AND THROMBOSIS, 2003, 33 (5-6) :495-499
[10]   The clinical features, risk factors and outcome of thrombotic thrombocytopenic purpura occurring after bone marrow transplantation [J].
Fuge, R ;
Bird, J M ;
Fraser, A ;
Hart, D ;
Hunt, L ;
Cornish, JM ;
Goulden, N ;
Oakhill, A ;
Pamphilon, DH ;
Steward, CG ;
Marks, DI .
BRITISH JOURNAL OF HAEMATOLOGY, 2001, 113 (01) :58-64