T细胞全血细胞移植后GVHD预防三种策略的比较:TACROLIMUS与钙神经抑制剂-MMF与SIROLIMUS-MMF。

IF 4.7 3区 医学 Q2 HEMATOLOGY Transplantation and Cellular Therapy Pub Date : 2024-10-01 Epub Date: 2024-08-06 DOI:10.1016/j.jtct.2024.07.027
Albert Esquirol , Maria Jesus Pascual , Juan Montoro , José Luis Piñana , Christelle Ferrà , Beatriz Herruzo , Irene Garcia-Cadenas , Aitana Balaguer , Ariadna Perez , Maria Huguet , Sara Redondo , Marta Villalba , Juan Carlos Hernandez-Boluda , Pedro Chorao , Rafael Hernani , Jaime Sanz , Carlos Solano , Jorge Sierra , Rodrigo Martino
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引用次数: 0

摘要

自移植后环磷酰胺(PTCy)问世以来,单倍体造血干细胞移植(HaploSCT)已成为缺乏其他合格供体的患者的真正选择。PTCy 后的标准 GvHD 预防疗法是钙神经蛋白抑制剂加 MMF(至第+35 天),但最近发表的西罗莫司(+/- MMF)和单剂他克莫司的治疗结果令人鼓舞。本项多中心回顾性研究比较了372例成人HaploSCT受者的治疗结果,这些受者接受了TBF调理、PTCY和额外的GVHD预防治疗,并采用了三种策略中的一种,即队列A:单药他克莫司(222例)、队列B:CNI-MMF(49例)和队列C:西罗莫司-MMF(101例)。100天时,II-IV级(20%、25%和30%)和III-IV级(9%、6%和15%)副坏死发生率无差异。不过,A 组的总体 cGvHD 发生率最低[分别为 24%、47% 和 52%(P 0.001)],中度-重度 cGvHD 发生率最低[分别为 13%、35% 和 33%(P 0.001)]。各组间的 3 年总生存期、无进展生存期、NRM 和复发率均无差异。总之,我们的研究表明,单药他克莫司、CNI+MMF 和西罗莫司+MMF GvHD 预防可导致 TBF 和 PTCy HaploSCT 后相似的结果,III-IV 级 aGvHD 发生率较低,但 cGVHD 方面可能存在的差异仍需进一步研究。
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Comparison of Three Graft-versus-Host Disease Prophylaxis Strategies after T Cell-Replete Haploidentical Hematopoietic Transplantation: Tacrolimus versus Calcineurin Inhibitors + Mycophenolate Mofetil versus Sirolimus + Mycophenolate Mofetil
Since the introduction of post-transplantation cyclophosphamide (PTCy), haploidentical hematopoietic stem cell transplantation (haploSCT) has become a real alternative for patients who lack other eligible donors. The standard graft-versus-host disease (GVHD) prophylaxis after PTCy has been a calcineurin inhibitor (CNI) plus mycophenolate mofetil (MMF) (up to day +35), but promising results with sirolimus (with or without MMF) and single-agent tacrolimus have been published recently. This multicenter retrospective study compared the outcomes of 372 adult haploSCT recipients who received conditioning with thiotepa, busulfan, and fludarabine (TBF), PTCy, and additional GVHD prophylaxis with 1 of 3 strategies: cohort A, single-agent tacrolimus (n = 222); cohort B, CNI + MMF (n = 49); or cohort C, sirolimus + MMF (n = 101). No differences among the 3 cohorts were found in terms of grade II-IV acute GVHD (20% in cohort A, 25% in cohort B, and 30% in cohort C) or grade III-IV acute GVHD (9%, 6%, and 15%, respectively) at 100 days; however, cohort A had the lowest incidence of overall chronic GVHD (24%, 47%, and 52%, respectively; P = .001) and moderate-severe chronic GVHD (13%, 35%, and 33%, respectively; P = .001). There were no differences in 3-year overall survival, progression-free survival, nonrelapse mortality, or relapse among the 3 cohorts. Overall, our study suggests that single-agent tacrolimus, CNI + MMF, and sirolimus + MMF GVHD prophylaxis lead to similar outcomes following haploSCT with TBF and PTCy, with a low incidence of grade III-IV acute GVHD, although possible differences in chronic GVHD require further investigation.
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