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亲缘供者移植:移植后环磷酰胺是否消除了 HLA 错配的有害影响?

Related donor transplants: has posttransplantation cyclophosphamide nullified the detrimental effect of HLA mismatch?

机构信息

The Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins Hospital, Baltimore, MD.

Division of Biostatistics, Institute for Health and Society, and.

出版信息

Blood Adv. 2018 Jun 12;2(11):1180-1186. doi: 10.1182/bloodadvances.2018018291.

Abstract

We sought to identify whether posttransplantation cyclophosphamide (PT-Cy) reduces or eliminates the detrimental impact of HLA mismatching on outcomes of HLA-haploidentical related donor transplantation for acute leukemia. Data from 2143 donor-recipient pairs (n = 218 haploidentical sibling; n = 218 offspring; n = 1707 HLA-matched sibling) with acute myeloid or lymphoblastic leukemia were studied. All received a calcineurin inhibitor for graft-versus-host disease (GVHD) prophylaxis while high-dose PT-Cy was also given to recipients of haploidentical transplant. Patient age correlated with donor-recipient relationship: haploidentical siblings donated to patients aged 18 to 54 years whereas offspring donated to patients aged 55 to 76 years. Therefore, transplant outcomes were examined separately in the 2 patient age groups. In patients aged 18 to 54 years, there were no significant differences in outcomes except chronic GVHD, which was lower after haploidentical sibling compared to HLA-matched sibling transplant (hazard ratio [HR], 0.63; < .001). In patients aged 55 to 76 years, despite lower chronic GVHD (HR, 0.42; < .001), graft failure (14% vs 6%; = .003), nonrelapse mortality (HR, 1.48; = .02), and overall mortality (HR, 1.32; = .003) were higher after transplant from offspring compared with an HLA-matched sibling. These data demonstrate a superior outcome in older recipients when using an HLA-matched sibling instead of offspring, although there were differences in transplant platforms (GVHD prophylaxis and graft type) between the 2 groups. Validation of these findings requires a prospective randomized trial wherein the transplant platforms can be closely matched.

摘要

我们试图确定移植后环磷酰胺 (PT-Cy) 是否降低或消除 HLA 错配对 HLA 单倍体相关供体移植治疗急性白血病结局的不利影响。研究了 2143 对供体-受体对(n = 218 个单倍体同胞;n = 218 个后代;n = 1707 个 HLA 匹配的同胞)的数据,这些患者患有急性髓系或淋巴母细胞白血病。所有患者均接受钙调神经磷酸酶抑制剂预防移植物抗宿主病(GVHD),而单倍体移植的受者也接受高剂量 PT-Cy。患者年龄与供体-受体关系相关:单倍体同胞供体为年龄 18 至 54 岁的患者,而后代供体为年龄 55 至 76 岁的患者。因此,分别检查了 2 个患者年龄组的移植结局。在年龄 18 至 54 岁的患者中,除慢性 GVHD 外,结局无显著差异,单倍体同胞移植后慢性 GVHD 发生率低于 HLA 匹配同胞移植(风险比 [HR],0.63;<0.001)。在年龄 55 至 76 岁的患者中,尽管慢性 GVHD 发生率较低(HR,0.42;<0.001),但移植后发生移植物衰竭(14% vs 6%;=0.003)、非复发死亡率(HR,1.48;=0.02)和总死亡率(HR,1.32;=0.003)较高,后代供体移植后高于 HLA 匹配的同胞。这些数据表明,在使用 HLA 匹配的同胞而不是后代时,老年受者的结局更好,尽管两组之间存在移植平台(GVHD 预防和移植物类型)的差异。这些发现需要前瞻性随机试验来验证,其中可以密切匹配移植平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8230/5998932/bc96c8af71fc/advances018291absf1.jpg

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