Risk Factors for the Incidence of and the Mortality due to Post-Transplant Lymphoproliferative Disorder after Hematopoietic Cell Transplantation

被引:15
|
作者
Kinzel, Megan [1 ]
Dowhan, Michelle [2 ]
Kalra, Amit [1 ]
Williamson, Tyler S. [1 ]
Dabas, Rosy [1 ]
Jamani, Kareem [1 ,2 ]
Chaudhry, Ahsan [1 ,2 ]
Shafey, Mona [1 ,2 ]
Jimenez-Zepeda, Victor [1 ,2 ]
Duggan, Peter [1 ,2 ]
Daly, Andrew [1 ,2 ]
Dharmani-Khan, Poonam [1 ,2 ,3 ]
Khan, Faisal [1 ,2 ,3 ]
Storek, Jan [1 ,2 ]
机构
[1] Univ Calgary, Cumming Sch Med, Calgary, AB, Canada
[2] Alberta Hlth Serv, Calgary, AB, Canada
[3] Alberta Precis Labs, Calgary, AB, Canada
来源
TRANSPLANTATION AND CELLULAR THERAPY | 2022年 / 28卷 / 01期
关键词
Post-transplantation lympho-proliferative disorder; Risk factor; Incidence; Mortality; ANTI-THYMOCYTE GLOBULIN; BONE-MARROW-TRANSPLANTATION; TOTAL-BODY IRRADIATION; VIRUS-DNA LEVELS; BLOOD STEM-CELL; PERIPHERAL-BLOOD; IMMUNE RECONSTITUTION; VIRAL LOAD; DISEASE; SEROSTATUS;
D O I
10.1016/j.jtct.2021.09.021
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Post-transplant lymphoproliferative disorder (PTLD) is a potentially serious complication that occurs following hematopoietic cell transplantation (HCT), in which B cells transformed by Epstein-Barr virus (EBV) proliferate uncontrollably. It is unknown whether risk factors for the incidence of PTLD are identical to those for mortality due to PTLD, a clinically more important outcome. We sought to determine the risk factors influencing the incidence of PTLD and those influencing mortality due to PTLD in a cohort of 1184 allogenic HCT recipients. All patients were predisposed to PTLD, because their graft-versus-host disease (GVHD) prophylaxis included antithymocyte globulin. The overall PTLD incidence was 9.0%, and mortality due to PTLD was 1.1%. In multivariate analysis, risk factors for PTLD incidence include donor+/recipient-(D+/R-) EBV serostatus (subhazard ratio [SHR], 3.3; P = .002), use of a donor other than an HLA-matched sibling donor (non-MSD) (SHR, 1.7; P = .029), receipt of total body irradiation (TBI; SHR, 3.3; P = .008), and the absence of GVHD (SHR, 3.3; P < .001). The sole risk factor for mortality due to PTLD among all patients was D+/R-serostatus (SHR, 5.8; P = .022). Risk factors for mortality due to PTLD among patients who developed PTLD were use of a bone marrow (BM) graft (compared with peripheral blood stem cells [PBSCs]; SHR, 22.8; P < .001) and extralymphatic involvement (SHR, 14.6; P < .001). Interestingly, whereas the absence of GVHD was a risk factor for PTLD incidence, there was a trend toward the presence of GVHD as a risk factor for PTLD mortality (SHR, 4.2; P = .093). Likewise, whereas use of a BM graft was a risk factor for PTLD mortality, there was a trend toward use of a PBSC graft as a risk factor for PTLD incidence (SHR, 0.44; P = .179). Some risk factors for the incidence of PTLD are identical to the risk factors for mortality due to PTLD (ie, D+/R-serostatus), whereas other risk factors are disparate. Specifically, TBI was identified as a risk factor for PTLD incidence but not for PTLD mortality; the absence of GVHD was a risk factor for PTLD incidence, whereas the presence of GVHD was possibly a risk factor for PTLD mortality; and receipt of a PBSC graft was possibly a risk factor for PTLD incidence, whereas receipt of a BM graft was a risk factor for PTLD mortality. <(c)> 2021 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:53.e1 / 53.e10
页数:10
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