Tocilizumab for the treatment of chimeric antigen receptor T cell-induced cytokine release syndrome

被引:288
作者
Kotch, Chelsea [1 ]
Barrett, David [1 ]
Teachey, David T. [1 ]
机构
[1] Univ Penn, Dept Pediat, Div Oncol, Childrens Hosp Philadelphia,Perelman Sch Med, Philadelphia, PA 19104 USA
关键词
Chimeric antigen receptor T cells (CAR T); chimeric antigen receptor T cell related encephalopathy syndrome (CRES); cytokine release syndrome (CRS); hemophagocytic lymphohistiocytosis (HLH); immune effector cell-associated neurotoxicity syndrome (ICANS); interleukin 6 (IL-6); neurotoxicity (NT); tisagenlecleucel; tocilizumab; ACUTE LYMPHOBLASTIC-LEUKEMIA; ADOPTIVE IMMUNOTHERAPY; B-ALL; THERAPY; ACTIVATION; BLINATUMOMAB; TRANSPLANTATION; NEUROTOXICITY; ENCEPHALITIS; BIOMARKERS;
D O I
10.1080/1744666X.2019.1629904
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction: Cancer-directed immunotherapies are transforming the landscape in oncology as new and exciting therapies move from the laboratory to the bedside. Chimeric antigen receptor T (CAR-T) cells are one of these novel therapies, demonstrating impressive efficacy against B-cell malignancies. With the development of new therapies, it is not uncommon to identify new and unanticipated toxicities. CAR-T cells cause unique toxicities not typically found with traditional cytotoxic chemotherapy or small molecule inhibitors. Areas covered: CAR-T cell associated toxicities include cytokine release syndrome (CRS) and CAR-T cell-related encephalopathy syndrome (CRES), alternatively known as immune effector cell-associated neurotoxicity syndrome (ICANS). Prompt identification and management of CRS and CRES are imperative for the prevention of life-threatening complications of these innovative therapies. This literature review describes the seminal trials of CD19-directed immunotherapy and the pathophysiology and management of the toxicities found with CAR-T cells. In addition, the use of the interleukin-6 receptor antibody tocilizumab for CRS is reviewed. Expert opinion: This review describes the recommended management of CRS and CRES and examines the current limitations in management. Alternative therapies for the treatment of CAR-T cell related toxicities are also explored. Furthermore, the review proposes future directions for research.
引用
收藏
页码:813 / 822
页数:10
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