Cytokine release syndrome in cancer immunotherapy with chimeric antigen receptor engineered T cells

被引:167
作者
Xu, Xiao-Jun
Tang, Yong-Min [1 ]
机构
[1] Zhejiang Univ, Div Hematol Oncol, Sch Med, Childrens Hosp, Hangzhou 310003, PR, Peoples R China
基金
中国国家自然科学基金;
关键词
Chimeric antigen receptor; Cytokine release syndrome; Cancer; Adverse event; Safety; MACROPHAGE ACTIVATION SYNDROME; MONOCLONAL-ANTIBODY RITUXIMAB; CHRONIC LYMPHOCYTIC-LEUKEMIA; VERSUS-HOST-DISEASE; ANTITUMOR-ACTIVITY; CLINICAL-TRIAL; ADOPTIVE IMMUNOTHERAPY; SIGNALING DOMAIN; ADVERSE EVENT; SUICIDE GENE;
D O I
10.1016/j.canlet.2013.10.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Adoptive transfer of chimeric antigen receptor (CAR)-engineered T cells is a promising therapy for cancers. However, the safety of this approach is concerned. Cytokine release syndrome (CRS) is a common but lethal complication of CAR-T cell therapy. The development of CRS correlates with CAR structures, tumor type and burden, and patients' genetic polymorphisms. CRS related adverse events may be reduced by designing safer CARs and CAR-T cells and following strict dose-escalation scheme. Timely and effective cytokine-directed treatment with corticosteroid and various cytokine antagonists is important to avoid CRS associated death. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:172 / 178
页数:7
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