Endothelial Activation and Stress Index in adults undergoing allogeneic hematopoietic cell transplantation with post-transplant cyclophosphamide-based prophylaxis

被引:6
作者
Escribano-Serrat, Silvia [1 ,2 ]
Rodriguez-Lobato, Luis Gerardo [2 ]
Charry, Paola [2 ]
Martinez-Cibrian, Nuria [2 ]
Suarez-Lledo, Maria [2 ]
Rivero, Andrea [2 ]
Moreno-Castano, Ana Belen [3 ]
Solano, Maria Teresa [2 ]
Arcarons, Jordi [2 ]
Nomdedeu, Meritxell [2 ]
Cid, Joan [4 ]
Lozano, Miquel [2 ]
Pedraza, Alexandra [2 ]
Rosinol, Laura [2 ]
Esteve, Jordi [2 ]
Urbano-Ispizua, Alvaro [2 ]
Palomo, Marta [2 ]
Fernandez-Aviles, Francesc [2 ]
Martinez, Carmen [2 ]
Diaz-Ricart, Maribel [3 ]
Carreras, Enric [5 ]
Rovira, Montserrat
Salas, Maria Queralt [2 ,6 ]
机构
[1] Hosp Clin San Carlos, Dept Hematol & Hemotherapy, IdiSSC, Madrid, Spain
[2] Hosp Clin Barcelona, Clin Inst Hematol & Oncol ICMHO, Hematol Dept, Hematopoiet Transplantat Unit, Barcelona, Spain
[3] Univ Barcelona, Hosp Clin Barcelona, IDIBAPS, Dept Pathol, Barcelona, Spain
[4] Hosp Clin Barcelona, Clin Inst Hematol & Oncol, Dept Hemotherapy & Hemostasis, Apheresis & Cellular Therapy Unit,IDIBAPS, Barcelona, Spain
[5] Fundańo i Inst Recerca Josep Carreras Leuce, Campus Clin, Barcelona, Spain
[6] Clin Inst Hematol & Oncol, Hematol Dept, Hosp Clin Barcelona, Hematopoiet Transplantat Unit, C Villarroel 190, Barcelona 08036, Spain
关键词
allogeneic hematopoietic cell transplantation; EASIX; endothelial complications; outcomes; post-transplant cyclophosphamide; prediction; EASIX; ADMISSION; BIOMARKER; RELEASE; DISEASE;
D O I
10.1016/j.jcyt.2023.10.008
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background aims: Post-transplant cyclophosphamide (PTCY)-based prophylaxis is becoming widespread for allogeneic hematopoietic cell transplantation (allo-HCT) performed independently of the selected donor source. In parallel, use of the Endothelial Activation and Stress Index (EASIX)-considered a surrogate parameter of endothelial activation-for predicting patient outcomes and clinical complications is gaining popularity in the allo-HCT setting. Methods: We first investigated whether the dynamics of EASIX after allo-HCT differ between patients receiving PTCY and patients receiving other prophylaxis. We then investigated whether the predictive capacity of EASIX persists in PTCY-based allo-HCT. A total of 328 patients transplanted between 2014 and 2020 were included, and 201 (61.2%) received PTCY. Results: EASIX trends differed significantly between the groups. Compared with patients receiving other prophylaxis, patients receiving PTCY had lower EASIX on day 0 and higher values between day 7 and day 100. In patients receiving PTCY, higher EASIX correlated significantly with higher non-relapse mortality (NRM) and lower overall survival (OS) when measured before and during the first 180 days after allo-HCT. In addition, higher EASIX scores measured at specific time points were predictors of veno-occlusive disease (VOD), transplant-associated thrombotic microangiopathy (TA-TMA) and grade 2-4 acute graft-versus-host disease (aGVHD) risk. Conclusions: This study demonstrates how EASIX trends vary during the first 180 days after allo-HCT in patients receiving PTCY and those not receiving PTCY and validates the utility of this index for predicting NRM, OS and risk of VOD, TA-TMA and grade 2-4 aGVHD in patients receiving PTCY. (c) 2023 International Society for Cell & Gene Therapy. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:73 / 80
页数:8
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