Impact of Cytomegalovirus Replication in Patients with Aggressive B Cell Lymphoma Treated with Chimeric Antigen Receptor T Cell Therapy

被引:24
|
作者
Marquez-Algaba, Ester [1 ,2 ]
Iacoboni, Gloria [2 ,3 ]
Pernas, Berta [4 ]
Esperalba, Juliana [5 ]
Los Arcos, Ibai [1 ]
Navarro, Victor [6 ]
Monforte, Arnau [1 ,2 ]
Beas, Francisco [3 ]
Albasanz-Puig, Adaia
Carpio, Cecilia [2 ,3 ]
Barba, Pere [2 ,3 ,7 ]
Ruiz-Camps, Isabel [1 ,2 ]
机构
[1] Univ Hosp Vall dHebron, Vall dHebron Res Inst, Dept Infect Dis, Barcelona, Spain
[2] Univ Autonoma Barcelona, Dept Med, Bellaterra, Spain
[3] Univ Hosp Vall dHebron, Vall dHebron Inst Oncol, Dept Hematol, Barcelona, Spain
[4] Univ Hosp A Coruna, Biomed Res Inst Coruna, Dept Infect Dis, Clin Virol Grp, La Coruna, Spain
[5] Univ Hosp Vall dHebron, Vall dHebron Res Inst, Dept Microbiol, Barcelona, Spain
[6] Vall dHebron Inst Oncol, Oncol Data Sci ODysSey Grp, Barcelona, Spain
[7] Hosp Univ Vall dHebron, Dept Hematol, Passeig Vall Hebron 119, Barcelona 08035, Spain
来源
TRANSPLANTATION AND CELLULAR THERAPY | 2022年 / 28卷 / 12期
关键词
Key Cytomegalovirus replication; Cytomegalovirus surveillance; CART cell therapy; Aggressive B cell lymphoma; INFECTIOUS COMPLICATIONS; DISEASE;
D O I
10.1016/j.jtct.2022.09.007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Data are scarce on cytomegalovirus (CMV) replication in patients receiving CD19-directed chimeric antigen receptor (CAR) T cell treatment. Here we describe the incidence, severity, and management of CMV infection in patients with aggressive B cell lymphoma treated with CAR T cell therapy. In this retrospective observational study, we analyzed CMV viral load and its clinical impact in patients with aggressive B cell lymphoma receiving CAR T cell therapy between July 2018 and December 2021 at a single center. Patients with a negative baseline CMV IgG or a previous allogeneic stem cell transplantation were excluded. CMV replication was determined in whole blood. Overall, 105 patients met the study's inclusion criteria. Ten patients presented with CMV replication before CAR T cell infusion and were analyzed separately. Forty-two of the remaining 95 patients (44%) had at least 1 positive CMV determination, with a viral load >1000 IU/mL in 21 patients (22%). Four patients in the main cohort (N = 95) and 4 patients in the preinfusion replication group (N = 10) achieved a viral load >10,000 IU/mL. Only 7 patients received preemptive anti-viral treatment. No CMV end-organ disease was reported. The sole independent risk factor associated with CMV vire-mia >1000 IU/mL was dexamethasone treatment (odds ratio, 8.4; 95% confidence interval, 2.4 to 36.6; P = .002). Based on our findings, we designed an algorithm for CMV management in this setting. CMV replication is relatively frequent in patients with aggressive B cell lymphoma receiving CART cell therapy. It is usually self-limited and not associated with end-organ disease. Patients receiving dexamethasone or harboring CMV replication before infusion might benefit from active surveillance and preemptive treatment strategies. (c) 2022 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:851.e1 / 851.e8
页数:8
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