Department of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Germany.
Department of Bone Marrow Transplantation, West German Cancer Center, University Hospital Essen, Essen, Germany; DRST - German Registry for Stem Cell Transplantation, Essen, Germany.
Biol Blood Marrow Transplant. 2018 Dec;24(12):2558-2567. doi: 10.1016/j.bbmt.2018.06.026. Epub 2018 Jul 24.
Increasing donor-recipient HLA disparity is associated with negative outcomes of allogeneic hematopoietic stem cell transplantation (HSCT), but its comparative relevance amid non-HLA donor characteristics is not well established. We addressed this question in 3215 HSCTs performed between 2005 and 2013 in Germany for acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS). Donors were HLA-matched related (MRD; n = 872) or unrelated (10/10 MUD, n = 1553) or HLA-mismatched unrelated (<10/10 MMUD, n = 790). Overall survival (OS) was similar after MRD compared with 10/10 MUD HSCT, reflecting opposing hazards of relapse (hazard ratio [HR], 1.32; P < .002) and nonrelapse mortality (HR, .63; P < .001). After UD HSCT, increasing HLA disparity was associated with inferior OS (HR, 1.21 [P < .02] and HR, 1.57 [P < .001] for 9/10 and ≤8/10 MMUD, respectively, compared with 10/10 MUD). Among non-HLA donor characteristics, age, sex mismatching (male recipient-female donor), and cytomegalovirus (CMV) mismatching (positive recipient-negative donor) impacted OS. Multivariate subgroup analysis showed that OS was similar after HSCT from the youngest 9/10 MMUD (<30 years) compared with the oldest 10/10 MUD (>40 years) (HR, 1.18; P = .25) and also in male patients transplanted from female 10/10 MUD compared with male 9/10 MMUD (HR, .89; P = .46). In contrast, OS of CMV-positive patients tended to be better with CMV-negative 10/10 MUDs compared with CMV-positive 9/10 MMUDs (HR, 1.31; P = .04). Because of low patient numbers in subgroups, definite conclusions and establishment of a hierarchy among HLA matching and non-HLA donor characteristics could not be made. Our data suggest that the impact of donor age and sex mismatch but not CMV mismatch on outcome of allogeneic HSCT may be comparable with that of single HLA disparity.
在异基因造血干细胞移植(HSCT)中,供受者 HLA 差异增加与移植结局不良相关,但在非 HLA 供者特征中,其相对相关性尚未得到充分证实。我们在德国 2005 年至 2013 年间进行的 3215 例急性髓系白血病(AML)或骨髓增生异常综合征(MDS)异基因 HSCT 中研究了这一问题。供者为 HLA 匹配的亲缘供者(MRD,n=872)或无关供者(10/10 单倍体相合无关供者,n=1553)或 HLA 错配的无关供者(<10/10 单倍体不全相合无关供者,n=790)。MRD 与 10/10 单倍体相合无关供者 HSCT 相比,总生存率(OS)相似,这反映了复发(危险比 [HR],1.32;P<.002)和非复发死亡率(HR,.63;P<.001)的风险相反。在 UD HSCT 后,随着 HLA 差异的增加,OS 降低(HR,1.21[P<.02]和 HR,1.57[P<.001],分别为 9/10 和≤8/10 MMUD 与 10/10 MUD 相比)。在非 HLA 供者特征中,年龄、性别不匹配(男性受者-女性供者)和巨细胞病毒(CMV)不匹配(阳性受者-阴性供者)影响 OS。多变量亚组分析显示,与年龄最大的 10/10 MUD(>40 岁)相比,年龄最小的 9/10 MMUD(<30 岁)(HR,1.18;P=.25)和男性患者从女性 10/10 MUD 移植与男性 9/10 MMUD 相比(HR,.89;P=.46),OS 相似。相反,CMV 阳性患者的 CMV 阴性 10/10 MUD 与 CMV 阳性 9/10 MMUD 相比,OS 趋势更好(HR,1.31;P=.04)。由于亚组患者数量较少,因此无法得出 HLA 匹配和非 HLA 供者特征之间的明确结论和层次关系。我们的数据表明,供者年龄和性别不匹配的影响,但 CMV 不匹配的影响可能与单个 HLA 差异相当。