Severity and organ distribution of graft-versus-host disease with post-transplant cyclophosphamide versus calcineurin inhibitor plus methotrexate/mycophenolate mofetil or sirolimus in allogenic HLA-matched or single-allele mismatched stem cell transplantation

被引:0
|
作者
Redondo, Sara [1 ,2 ]
Garcia-Cadenas, Irene [1 ,2 ]
Esquirol, Albert [1 ,2 ]
Portos, J. M. [1 ,2 ]
Iranzo, Eva [1 ,2 ]
Arguello-Tomas, Miguel [1 ,2 ]
Saavedra, Silvana [1 ,2 ]
Onate, Guadalupe [1 ,2 ]
Caballero, Ana-Carolina [1 ,2 ]
Garrido, Ana [1 ,2 ]
Lopez, Jordi [1 ,2 ]
Muntanola, Ana [1 ,2 ]
Paviglianiti, Annalisa [1 ,2 ]
Miqueleiz, Sara [1 ,2 ]
Sierra, Jorge [1 ,2 ]
Briones, Javier [1 ,2 ]
Martino, Rodrigo [1 ,2 ]
机构
[1] Hosp Santa Creu & Sant Pau, IIB St Pau & Jose Carreras Leukemia Res Inst, Hematol Dept, Barcelona, Spain
[2] Univ Autonoma Barcelona, Dept Med, Barcelona, Spain
关键词
allogeneic hematopoietic cell transplant; GvHD; non-relapse mortality; post-transplant cyclophosphamide; BONE-MARROW-TRANSPLANTATION; MYCOPHENOLATE-MOFETIL; GVHD PROPHYLAXIS; MYELOID-LEUKEMIA; TACROLIMUS; BLOOD; FLUDARABINE; MORTALITY; METHOTREXATE; CYCLOSPORINE;
D O I
10.1111/ejh.14294
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: This retrospective single center study aims to describe changes in the severity and organ-specific distribution of GvHD, by comparing the outcomes of 3 distinct GvHD prophylaxis approaches. Methods: Between January 2012 and June 2022, 226 patients underwent allogeneic hematopoietic stem cell transplantation from HLA-matched or 1-allele mismatched related or unrelated donors. Fifty-eight (26%) received prophylaxis with calcineurin inhibitor in combination with mycophenolate mofetil or a short course of methotrexate (Cohort-1), 87 (38%) tacrolimus plus sirolimus (Cohort-2), and 81 (36%) post-transplant cyclophosphamide (PTCy) plus tacrolimus (Cohort-3). Results: The incidence of grade II-IV aGvHD was 69% vs. 41.4% vs. 27.2%; p < .01. The most significant reduction with PTCy was observed in both stage 3-4 skin and lower gastrointestinal (GI) involvement (p < .01). The incidence of moderate-to-severe cGvHD at 12 months was 34.5% vs. 34.5% vs. 6.2%; p < .01. Moderate-to-severe skin and GI cGvHD was less common after PTCy (p < .01). The 1-year GvHD-free/relapse-free survival was higher with PTCy (p < .01). Conclusions: Our study indicates that PTCy-based GvHD prophylaxis reduces the frequency and severity of both acute and chronic GvHD, with a notable decrease in severe GI and cutaneous manifestations. The higher GRFS may result in lower GvHD-related mortality, leading to an improved quality of life among survivors.
引用
收藏
页码:776 / 787
页数:12
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