Hematopoietic stem cell transplantation:: contrasting the outcome of transplantations from HLA-identical siblings, partially HLA-mismatched related donors, and HLA-matched unrelated donors

被引:84
作者
Ottinger, HD
Ferencik, S
Beelen, DW
Lindemann, M
Peceny, R
Elmaagacli, AH
Hüsing, J
Grosse-Wilde, H
机构
[1] Univ Hosp Essen, Inst Immunol, Dept Bone Marrow Transplantat, D-45147 Essen, Germany
[2] Univ Hosp Essen, Inst Med Informat Biometry & Epidemiol, D-45147 Essen, Germany
关键词
D O I
10.1182/blood-2002-09-2866
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Allogeneic hematopoietic stem cell transplantation (HSCT) is a proven curative therapy for many hematologic malignancies. HSCT from HLA-identical sibling donors (ISDs) is still the golden standard. For the remaining 70% of the patients lacking an ISD, alternative (partially) HLA-matched family donors (MFDs) and HLA-matched unrelated donors (MUDs) are now widely accepted. However, it is presently unclear whether outcome after HSCT from an MFD or an MUD is superior. Thus, the classical clinical end points after HSCT from an ISD (n = 138), MFD (n = 86), and MUD (n = 101) were compared by means of univariate and multivariate statistical analyses. MFD transplantations with HLA class II (DRB1 +/- DQB1) mismatches in graft-versus-host (GVH) direction showed an increased risk of grades II to IV graft-versus-host disease, and MFD transplantations with more than a single HLA class I (A +/- B +/- C) mismatch in host-versus-graft (HVG) direction were associated with a higher risk of graft failure. However, no significant difference in overall survival was detectable among the 3 study groups after adjustment for the main predictors of transplantation outcome. Thus, for patients lacking an ISD, an already identified MFD with an HLA-DRB1 +/- DQB1 mismatch in GVH or a combined HLA-A +/- B +/- C mismatch in HVG direction should be accepted only in clinically urgent settings that leave no time to identify an MUD.
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页码:1131 / 1137
页数:7
相关论文
共 32 条
[1]   EFFECT OF HLA COMPATIBILITY ON ENGRAFTMENT OF BONE-MARROW TRANSPLANTS IN PATIENTS WITH LEUKEMIA OR LYMPHOMA [J].
ANASETTI, C ;
AMOS, D ;
BEATTY, PG ;
APPELBAUM, FR ;
BENSINGER, W ;
BUCKNER, CD ;
CLIFT, R ;
DONEY, K ;
MARTIN, PJ ;
MICKELSON, E ;
NISPEROS, B ;
OQUIGLEY, J ;
RAMBERG, R ;
SANDERS, JE ;
STEWART, P ;
STORB, R ;
SULLIVAN, KM ;
WITHERSPOON, RP ;
THOMAS, ED ;
HANSEN, JA .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 320 (04) :197-204
[2]  
Anasetti C., 1999, HEMATOPOIETIC CELL T, P904
[3]   BONE-MARROW TRANSPLANTATION [J].
ARMITAGE, JO .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (12) :827-838
[4]  
BEELEN DW, 1992, BLOOD, V80, P2668
[5]   Transplantation of filgrastim-mobilized peripheral blood stem cells from HLA-identical sibling or alternative family donors in patients with hematologic malignancies: A prospective comparison on clinical outcome, immune reconstitution, and hematopoietic chimerism [J].
Beelen, DW ;
Ottinger, HD ;
Elmaagacli, A ;
Scheulen, B ;
Basu, O ;
Kremens, B ;
Havers, W ;
GrosseWilde, H ;
Schaefer, UW .
BLOOD, 1997, 90 (12) :4725-4735
[6]  
CLEAVER SA, 1993, BONE MARROW TRANSPL, V11, P38
[7]  
Davies SM, 2000, BLOOD, V96, P4096
[8]   HLA-C high resolution typing: analysis of exons 2 and 3 by sequence based typing and detection of polymorphisms in exons 1-5 by sequence specific primers [J].
Delfino, L ;
Morabito, A ;
Longo, A ;
Ferrara, GB .
TISSUE ANTIGENS, 1998, 52 (03) :251-259
[9]   THE GERMAN BONE-MARROW DATA-BASE [J].
EHNINGER, G ;
RUTT, CMA ;
EBERT, A ;
HARF, P ;
HOELZER, D ;
NIETHAMMER, D ;
VONKELLER, J ;
RODERT, A ;
SCHULER, U .
DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT, 1994, 119 (40) :1359-1364
[10]   CLINICAL MANIFESTATIONS OF GRAFT VERSUS HOST DISEASE IN HUMAN RECIPIENTS OF MARROW FROM HL-A-MATCHED SIBLING DONORS [J].
GLUCKSBERG, H ;
STORB, R ;
FEFER, A ;
BUCKNER, CD ;
NEIMAN, PE ;
CLIFT, RA ;
LERNER, KG ;
THOMAS, ED .
TRANSPLANTATION, 1974, 18 (04) :295-304