Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
Cell Transplant. 2020 Jan-Dec;29:963689720976567. doi: 10.1177/0963689720976567.
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.
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。