Eapen Mary, Wang Tao, Veys Paul A, Boelens Jaap J, St Martin Andrew, Spellman Stephen, Bonfim Carmem Sales, Brady Colleen, Cant Andrew J, Dalle Jean-Hugues, Davies Stella M, Freeman John, Hsu Katherine C, Fleischhauer Katharina, Kenzey Chantal, Kurtzberg Joanne, Michel Gerard, Orchard Paul J, Paviglianiti Annalisa, Rocha Vanderson, Veneris Michael R, Volt Fernanda, Wynn Robert, Lee Stephanie J, Horowitz Mary M, Gluckman Eliane, Ruggeri Annalisa
Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
Lancet Haematol. 2017 Jul;4(7):e325-e333. doi: 10.1016/S2352-3026(17)30104-7. Epub 2017 Jun 13.
The standard for selecting unrelated umbilical cord blood units for transplantation for non-malignant diseases relies on antigen-level (lower resolution) HLA typing for HLA-A and HLA-B, and allele-level for HLA-DRB1. We aimed to study the effects of allele-level matching at a higher resolution-HLA-A, HLA-B, HLA-C, and HLA-DRB1, which is the standard used for adult unrelated volunteer donor transplantation for non-malignant diseases-for umbilical cord blood transplantation.
We retrospectively studied 1199 paediatric donor-recipient pairs with allele-level HLA matching who received a single unit umbilical cord blood transplantation for non-malignant diseases reported to the Center for International Blood and Marrow Transplant Research or Eurocord and European Group for Blood and Marrow Transplant. Transplantations occurred between Jan 1, 2000, and Dec 31, 2012. The primary outcome was overall survival. The effect of HLA matching on survival was studied using a Cox regression model.
Compared with HLA-matched transplantations, mortality was higher with transplantations mismatched at two (hazard ratio [HR] 1·55, 95% CI 1·08-2·21, p=0·018), three (2·04, 1·44-2·89, p=0·0001), and four or more alleles (3·15, 2·16-4·58, p<0·0001). There were no significant differences in mortality between transplantations that were matched and mismatched at one allele (HR 1·18, 95% CI 0·80-1·72, p=0·39). Other factors associated with higher mortality included recipient cytomegalovirus seropositivity (HR 1·40, 95% CI 1·13-1·74, p=0·0020), reduced intensity compared with myeloablative conditioning regimens (HR 1·36, 1·10-1·68, p=0·0041), transplantation of units with total nucleated cell dose of more than 21 × 10 cells per kg compared with 21 × 10 cells per kg or less (HR 1·47, 1·11-1·95, p=0·0076), and transplantations done in 2000-05 compared with those done in 2006-12 (HR 1·64, 1·31-2·04, p<0·0001). The 5-year overall survival adjusted for recipient cytomegalovirus serostatus, conditioning regimen intensity, total nucleated cell dose, and transplantation period was 79% (95% CI 74-85) after HLA matched, 76% (71-81) after one allele mismatched, 70% (65-75) after two alleles mismatched, 62% (57-68) after three alleles mismatched, and 49% (41-57) after four or more alleles mismatched transplantations. Graft failure was the predominant cause of mortality.
These data support a change from current practice in that selection of unrelated umbilical cord blood units for transplantation for non-malignant diseases should consider allele-level HLA matching at HLA-A, HLA-B, HLA-C, and HLA-DRB1.
National Cancer Institute; National Heart, Lung, and Blood Institute; National Institute for Allergy and Infectious Diseases; US Department of Health and Human Services-Health Resources and Services Administration; and US Department of Navy.
选择非恶性疾病移植的无关脐血单位的标准依赖于 HLA - A 和 HLA - B 的抗原水平(低分辨率)HLA 分型,以及 HLA - DRB1 的等位基因水平分型。我们旨在研究更高分辨率的 HLA - A、HLA - B、HLA - C 和 HLA - DRB1 等位基因匹配(这是成人非恶性疾病无关志愿供者移植的标准)对脐血移植的影响。
我们回顾性研究了 1199 对接受单单位脐血移植治疗非恶性疾病的儿科供受者对,这些供受者对的 HLA 等位基因匹配情况已报告给国际血液和骨髓移植研究中心或 Eurocord 以及欧洲血液和骨髓移植组。移植发生在 2000 年 1 月 1 日至 2012 年 12 月 31 日之间。主要结局是总生存。使用 Cox 回归模型研究 HLA 匹配对生存的影响。
与 HLA 匹配的移植相比,两个等位基因不匹配(风险比[HR]1.55,95%置信区间 1.08 - 2.21,p = 0.018)、三个等位基因不匹配(2.04,1.44 - 2.89,p = 0.0001)以及四个或更多等位基因不匹配(3.15,2.16 - 4.58,p < 0.0001)的移植死亡率更高。一个等位基因匹配和不匹配的移植之间死亡率无显著差异(HR 1.18,95%置信区间 0.80 - 1.72,p = 0.39)。与较高死亡率相关的其他因素包括受者巨细胞病毒血清学阳性(HR 1.40,95%置信区间 1.13 - 1.74,p = 0.0020)、与清髓性预处理方案相比强度降低(HR 1.36,1.10 - 1.68,p = 0.0041)、每千克总核细胞剂量超过 21×10⁶ 个细胞的单位移植与每千克 21×10⁶ 个细胞或更少的单位移植相比(HR 1.47,1.11 - 1.95,p = 0.0076),以及 2000 - 2005 年进行的移植与 2006 - 2012 年进行的移植相比(HR 1.64,1.31 - 2.04,p < 关于受者巨细胞病毒血清状态、预处理方案强度、总核细胞剂量和移植时期进行调整后,HLA 匹配后的 5 年总生存率为 79%(95%置信区间 74 - 85),一个等位基因不匹配后为 76%(71 - 81),两个等位基因不匹配后为 70%(65 - 75),三个等位基因不匹配后为 62%(57 - 68),四个或更多等位基因不匹配移植后为 49%(41 - 57)。移植物失败是主要的死亡原因。
这些数据支持改变当前做法,即选择非恶性疾病移植的无关脐血单位时应考虑 HLA - A、HLA - B、HLA - C 和 HLA - DRB1 的等位基因水平 HLA 匹配。
美国国立癌症研究所;美国国立心肺血液研究所;美国国立过敏和传染病研究所;美国卫生与公众服务部 - 卫生资源和服务管理局;以及美国海军部。