Ottinger Hellmut D, Ferencik Stanislav, Beelen Dietrich W, Lindemann Monika, Peceny Rudolf, Elmaagacli Ahmed H, Husing Johannes, Grosse-Wilde Hans
Department of Bone Marrow Transplantation, Institute of Immunology, University Hospital of Essen, Essen, Germany.
Blood. 2003 Aug 1;102(3):1131-7. doi: 10.1182/blood-2002-09-2866. Epub 2003 Apr 10.
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.
异基因造血干细胞移植(HSCT)是治疗多种血液系统恶性肿瘤的一种已被证实的治愈性疗法。来自人类白细胞抗原(HLA)匹配的同胞供者(ISD)的HSCT仍是金标准。对于其余70%缺乏ISD的患者,替代的(部分)HLA匹配的家族供者(MFD)和HLA匹配的无关供者(MUD)目前已被广泛接受。然而,目前尚不清楚来自MFD或MUD的HSCT后的结果是否更优。因此,通过单因素和多因素统计分析比较了来自ISD(n = 138)、MFD(n = 86)和MUD(n = 101)的HSCT后的经典临床终点。在移植物抗宿主(GVH)方向存在HLA II类(DRB1 +/- DQB1)错配的MFD移植显示II至IV级移植物抗宿主病风险增加,而在宿主抗移植物(HVG)方向存在超过单个HLA I类(A +/- B +/- C)错配的MFD移植与更高的移植失败风险相关。然而,在对移植结果的主要预测因素进行调整后,3个研究组之间在总生存方面未检测到显著差异。因此,对于缺乏ISD的患者,只有在临床紧急情况下且没有时间识别MUD时,才应接受已确定的在GVH方向存在HLA - DRB1 +/- DQB1错配或在HVG方向存在联合HLA - A +/- B +/- C错配的MFD。