Reduced-Intensity Conditioning with Busulfan, Fludarabine, and Antithymocyte Globulin for Hematopoietic Cell Transplantation from Unrelated or Haploidentical Family Donors in Patients with Acute Myeloid Leukemia in Remission

被引:18
作者
Lee, Kyoo-Hyung [1 ]
Lee, Je-Hwan [1 ]
Lee, Jung-Hee [1 ]
Kim, Dae-Young [1 ]
Park, Han-Seung [1 ]
Choi, Eun-Ji [1 ]
Ko, Sun-Hye [1 ]
Seol, Miee [1 ]
Lee, Young-Shin [1 ]
Kang, Young-A [1 ]
Jeon, Mijin [1 ]
Baek, Seunghyun [1 ]
Kang, You-Lee [1 ]
Kim, Sung-Han [2 ]
Yun, Sung-Cheol [3 ]
Kim, Hawk [4 ]
Jo, Jae-Cheol [4 ]
Choi, Yunsuk [4 ]
Joo, Young -Don [5 ]
Sung-Nam Lim [5 ]
机构
[1] Univ Ulsan, Coll Med, Asan Med Ctr, Sect Hematol,Dept Internal Med, Seoul, South Korea
[2] Univ Ulsan, Coll Med, Asan Med Ctr, Sect Infect Dis,Dept Internal Med, Seoul, South Korea
[3] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Clin Epidemiol & Biostat, Seoul, South Korea
[4] Univ Ulsan, Coll Med, Ulsan Univ Hosp, Div Hematol & Cellular Therapy, Ulsan, South Korea
[5] Inje Univ, Coll Med, Haeundae Paik Hosp, Hematol Oncol,Dept Internal Med, Busan, South Korea
关键词
Acute myeloid leukemia; Allogeneic hematopoietic cell transplantation; Antithymocyte globulin; Busulfan; Fludarabine; HLA-matched unrelated donor; HLA-haploidentical family donor; HLA-matched sibling donor; VERSUS-HOST-DISEASE; BONE-MARROW-TRANSPLANTATION; ACUTE MYELOGENOUS LEUKEMIA; ANTI-THYMOCYTE-GLOBULIN; 1ST COMPLETE REMISSION; ACUTE GRAFT; HEMATOLOGIC MALIGNANCIES; HLA-A; POSTTRANSPLANTATION CYCLOPHOSPHAMIDE; CUMULATIVE INCIDENCE;
D O I
10.1016/j.bbmt.2017.05.025
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To investigate the role of antithymocyte globulin (ATG)-containing reduced-intensity conditioning (RIC) in hematopoietic cell transplantation (HCT) from unrelated (UD) or haploidentical family donors (RFD), we conducted a phase 2 trial of 237 patients (age range, 16 to 69 years) with acute myeloid leukemia (AML) in remission. Patients undergoing UD-HCT (n = 93) or HFD-HCT (n = 59) received RIC comprising busulfan, fludarabine, and ATG, 9 mg/kg, whereas those undergoing HCT from matched sibling donors (MSD, n = 85) received myeloablative busulfan and cyclophosphamide conditioning or aforementioned RIC with ATG, 4.5 mg/kg. For graft-versus host disease (GVHD) prophylaxis, cyclosporine and methotrexate were administered. The median follow-up period was 44.7 months after HCT for 161 survivors. For UD-HCT versus HFD-HCT, there were no significant differences in leukemia recurrence, nonrelapse mortality, relapse-free survival, grades 2 to 4 acute GVHD, and moderate-to-severe chronic GVHD. Furthermore, when the outcomes of UD-HCT and HFD-HCT were combined and compared with those of MSD-HCT, there were no significant differences in leukemia recurrence (3-year cumulative incidence, 30% versus 29%), nonrelapse mortality (3-year cumulative incidence, 7% versus 8%), relapse-free survival (3-year estimate, 63% versus 63%), and grades 2 to 4 acute GVHD (120-day cumulative incidence, 16% versus 13%). Moderate-to-severe chronic GVHD, however, occurred less frequently in UD/HFD-HCT (2-year cumulative incidence, 22% versus 40%; P=.006). The addition of ATG to conditioning regimen was a significant predictor for less chronic GVHD (subdistribution hazard ratio, .59). In AML in remission, UD/HFD-HCT after ATG-containing RIC achieved leukemia control equivalent to that of MSD-HCT. Despite HLA disparity in UD/HFD-HCT, chronic GVHD occurred less frequently after ATG-containing RIC, suggesting a strong GVHD-modulating effect of ATG. (C) 2017 American Society for Blood and Marrow Transplantation.
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收藏
页码:1555 / 1566
页数:12
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