Toxicity and management in CAR T-cell therapy Journal Article


Authors: Bonifant, C. L.; Jackson, H. J.; Brentjens, R. J.; Curran, K. J.
Article Title: Toxicity and management in CAR T-cell therapy
Abstract: T cells can be genetically modified to target tumors through the expression of a chimeric antigen receptor (CAR). Most notably, CAR T cells have demonstrated clinical efficacy in hematologic malignancies with more modest responses when targeting solid tumors. However, CAR T cells also have the capacity to elicit expected and unexpected toxicities including: cytokine release syndrome, neurologic toxicity, "on target/off tumor" recognition, and anaphylaxis. Theoretical toxicities including clonal expansion secondary to insertional oncogenesis, graft versus host disease, and off-target antigen recognition have not been clinically evident. Abrogating toxicity has become a critical step in the successful application of this emerging technology. To this end, we review the reported and theoretical toxicities of CAR T cells and their management.
Keywords: review; neurotoxicity; t lymphocyte; dexamethasone; carcinogenesis; hematologic malignancy; cardiotoxicity; antigen recognition; graft versus host reaction; chimeric antigen receptor; cell therapy; immunosuppressive treatment; anaphylaxis; ganciclovir; t lymphocyte activation; intracellular signaling; suicide gene; cytokine release syndrome; fk 506 binding protein; tocilizumab; human; priority journal
Journal Title: Molecular Therapy - Oncolytics
Volume: 3
ISSN: 2372-7705
Publisher: Cell Press  
Date Published: 2016-04-20
Start Page: 16011
Language: English
DOI: 10.1038/mto.2016.11
PROVIDER: scopus
PMCID: PMC5008265
PUBMED: 27626062
DOI/URL:
Notes: Review -- Export Date: 2 June 2016 -- Source: Scopus
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  1. Renier J Brentjens
    286 Brentjens
  2. Kevin Joseph Curran
    149 Curran
  3. Hollie Jaine Pegram
    19 Pegram