Characteristics and risk factors of infections following CD28-based CD19 CAR-T cells

被引:35
作者
Dayagi, Talya Wittmann [1 ,2 ]
Sherman, Gilad [1 ,2 ]
Bielorai, Bella [2 ,3 ]
Adam, Etai [3 ]
Besser, Michal J. [2 ,4 ]
Shimoni, Avichai [2 ,5 ]
Nagler, Arnon [2 ,5 ]
Toren, Amos [2 ,3 ]
Jacoby, Elad [2 ,3 ]
Avigdor, Abraham [2 ,5 ]
机构
[1] Edmond & Lily Safra Childrens Hosp, Sheba Med Ctr, Dept Pediat, Ramat Gan, Israel
[2] Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel
[3] Edmond & Lily Safra Childrens Hosp, Sheba Med Ctr, Div Pediat Hematol & Oncol, Ramat Gan, Israel
[4] Sheba Med Ctr, Ella Inst Immunooncol, Ramat Gan, Israel
[5] Sheba Med Ctr, Div Hematol & Bone Marrow Transplantat, Ramat Gan, Israel
关键词
CAR T-cells; leukemia; lymphoma; infections; cytokine-release syndrome;
D O I
10.1080/10428194.2021.1881506
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
CAR T-cells are approved for the treatment of relapsed and refractory leukemia and lymphoma. Here, we studied the infectious complications in 88 patients treated with CD28-based CD19 CAR T-cells. Overall, 36 infections were documented in 24 patients within the first month after CAR T-cell infusion: Six events of bacteremia, sixteen focal bacterial infections, and fourteen systemic or localized viral infections. Seven patients had nine infectious episodes beyond the first 30 days of follow-up, including three events of bacteremia, three focal bacterial, two viral and one fungal infection. The presence of neutropenia, neutropenic fever and lack of response to treatment were associated with a higher rate of infections. Children had less severe infections than adults. In a multivariate analysis lack of response to treatment was the only significant risk factor. Overall, the incidence of bacterial infections following CAR T-cells is modest especially in children and in patients responding to therapy.
引用
收藏
页码:1692 / 1701
页数:10
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