Posttransplantation cyclophosphamide vs. antithymocyte globulin as GVHD prophylaxis for mismatched unrelated hematopoietic stem cell transplantation

被引:24
作者
Nykolyszyn, Charlotte [1 ]
Granata, Angela [1 ]
Pagliardini, Thomas [1 ]
Castagna, Luca [2 ]
Harbi, Samia [1 ]
Bouabdallah, Reda [1 ]
Vey, Norbert [1 ,3 ]
Furst, Sabine [1 ]
Maisano, Valerio [1 ]
Legrand, Faezeh [1 ]
Lemarie, Claude [4 ,5 ]
Calmels, Boris [4 ,5 ]
Chabannon, Christian [3 ,4 ,5 ]
Weiller, Pierre-Jean [1 ]
Blaise, Didier [1 ,3 ]
Devillier, Raynier [1 ,3 ]
机构
[1] Inst Paoli Calmettes, Dept Hematol, Marseille, France
[2] Humanitas Canc Ctr, Dept Hematol, Rozzano, Italy
[3] Aix Marseille Univ, CNRS, INSERM, Inst Paoli Calmettes,CRCM, Marseille, France
[4] Inst Paoli Calmettes, Cell Therapy Facil, Marseille, France
[5] INSERM, CIC Biotherapies, CBT 1409, Marseille, France
关键词
VERSUS-HOST-DISEASE; BONE-MARROW-TRANSPLANTATION; OPEN-LABEL; HLA; DONOR; MALIGNANCIES; FLUDARABINE; PREVENTION; BUSULFAN; LEUKEMIA;
D O I
10.1038/s41409-019-0682-2
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Posttransplant cyclophosphamide (PT-Cy) is an efficient GVHD prophylaxis but has not been extensively evaluated in mismatched unrelated donor (MMUD) allo-HSCT, for which antithymocyte globulin (ATG) is still considered as a standard. Thus, we evaluated the outcome of MMUD allo-HSCT with PT-Cy (n = 22) and performed a historical comparison with a control group receiving ATG (n = 40) in a single center experience. Compared with the ATG group, the risk of grade 2-4 acute GVHD was significantly lower in the PT-Cy group (HR = 0.12, 95% CI = [0.03-0.48], p = 0.002). No difference was observed in the cumulative incidence of chronic GVHD. The risk of both NRM and relapse was significantly lower in the PT-Cy group (NRM: HR = 0.05, 95% CI = [0.00-0.63], p = 0.021; relapse: HR = 0.31; 95% CI = [0.09-1.10], p = 0.07). Thus, we observed significantly better PFS (HR = 0.22, 95% CI = (0.07-0.65); p = 0.006), OS (HR = 0.24, 95% CI = (0.07-0.84); p = 0.026), and GRFS (HR = 0.37, 95% CI = (0.17-0.80); p = 0.011) in the PT-Cy group. We conclude that PT-Cy is an effective GVHD prophylaxis in the setting of MMUD allo-HSCT, resulting in a better outcome compared with standard prophylaxis using ATG. This suggests that as it was shown in the setting of haploidentical allo-HSCT, the use of PT-Cy can overcome the impact of HLA disparity, leading to promising survivals that approach those observed after HLA matched allo-HSCT.
引用
收藏
页码:349 / 355
页数:7
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