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采用低剂量抗胸腺细胞球蛋白的 HLA1 配体错配相关供者造血干细胞移植移植物抗宿主病方向

Hematopoietic Stem Cell Transplantation From a Related Donor with Human Leukocyte Antigen 1-Antigen Mismatch in the Graft-Versus-Host Direction Using Low-dose Anti-thymocyte Globulin.

机构信息

Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.

出版信息

Cell Transplant. 2020 Jan-Dec;29:963689720976567. doi: 10.1177/0963689720976567.

Abstract

Hematopoietic stem cell transplantation (HSCT) from a related donor with an human leukocyte antigen (HLA) 1-antigen mismatch without in vivo T cell depletion is associated with an elevated risk of severe, acute, and chronic graft-versus-host (GVH) disease (GVHD) and poor survival. Therefore, we conducted a multicenter phase II trial of HSCT using low-dose anti-thymocyte globulin (ATG, thymoglobulin). We recruited patients aged 16-65 years with leukemia, myelodysplastic syndrome, or lymphoma who planned to receive HSCT from a related donor with HLA 1-antigen mismatch in the GVH direction at the HLA-A, -B, or -DR locus. Pretransplantation ATG was administered with standard GVHD prophylaxis consisting of tacrolimus and methotrexate. Thirty-eight patients were eligible for the analysis. The 1-year GVHD-free relapse-free survival (GRFS) was 47%. The 3-year overall survival (OS) was 57%. Age of less than 50 years was associated with better OS. OS in patients with high/very high refined disease risk indexes (rDRIs) was comparable to that in those with low/intermediate rDRIs. The 100-day cumulative incidences of grades II-IV and III-IV acute GVHD were 45% and 18%, respectively. HSCT from a related donor with two allele mismatches showed higher incidences of grades II-IV and III-IV acute GVHD. Three-year cumulative incidences of moderate to severe or severe chronic GVHD were 13% and 3%, respectively. HSCT from a related donor with one locus mismatch at the antigen level using low-dose ATG showed lower incidences of acute and chronic GVHD, which led to acceptable GRFS, OS, relapse, and nonrelapse mortality.

摘要

造血干细胞移植(HSCT)来自 HLA 1 抗原错配的相关供体,且未进行体内 T 细胞耗竭,与严重、急性和慢性移植物抗宿主病(GVHD)风险增加和生存不良相关。因此,我们进行了一项多中心 II 期临床试验,使用低剂量抗胸腺细胞球蛋白(ATG,胸腺球蛋白)进行 HSCT。我们招募了年龄在 16-65 岁之间的白血病、骨髓增生异常综合征或淋巴瘤患者,他们计划从 HLA-A、-B 或 -DR 位点 HLA 1 抗原错配的相关供体接受 HSCT。移植前给予 ATG,并采用他克莫司和甲氨蝶呤标准预防 GVHD。38 例患者符合分析条件。1 年无 GVHD 无复发生存率(GRFS)为 47%。3 年总生存率(OS)为 57%。年龄小于 50 岁与更好的 OS 相关。高/极高 refined disease risk indexes(rDRIs)患者的 OS 与低/中 rDRIs 患者相当。2 级-4 级和 3 级-4 级急性 GVHD 的 100 天累积发生率分别为 45%和 18%。两个等位基因错配的相关供体 HSCT 显示出更高的 2 级-4 级和 3 级-4 级急性 GVHD 发生率。3 年中至重度或重度慢性 GVHD 的累积发生率分别为 13%和 3%。使用低剂量 ATG 在抗原水平上进行一个位点错配的相关供体 HSCT 导致急性和慢性 GVHD 的发生率较低,从而获得可接受的 GRFS、OS、复发和非复发死亡率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fab1/7873771/6417a5d84094/10.1177_0963689720976567-fig1.jpg

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