Neurological adverse effects of chimeric antigen receptor T-cell therapy

Expert Rev Clin Immunol. 2023 Jul-Dec;19(11):1361-1383. doi: 10.1080/1744666X.2023.2248390. Epub 2023 Sep 4.

Abstract

Introduction: Chimeric antigen receptor (CAR) T-cell is among the most prevalent approaches that act by directing T-cells toward cancer; however, they need to be optimized to minimize side effects and maximize efficacy before being used as standard treatment for malignancies. Neurotoxicity associated with CAR T-cell therapy has been well-documented in recent works.

Areas covered: In this regard, two established syndromes exist. Immune effector cell-associated neurotoxicity syndrome (ICANS), previously called cytokine release encephalopathy syndrome (CRES), is a neuropsychiatric condition which can occur after therapy by immune effector cells (IEC) and T-lymphocytes utilizing treatments. Another syndrome is cytokine release syndrome (CRS), which may overlap with ICANS.

Expert opinion: ICANS clinical manifestations include cerebral edema, mild lethargy, aphasia, and seizures. Notably, ICANS is associated with changes to EEG and neuroradiological findings. Therefore, it is necessary to make a timely and accurate diagnosis of neurological complications of CAR T-cells by clinical presentations, neuroimaging, and EEG. Since neurological events by different CAR T-cell products are heterogeneous, guides should be developed according to each product. Here, we provide an updated review of general information on CAR T-cell therapies and applications, neurological syndromes associated with their use, and risk factors contributing to ICANS.

Keywords: Adoptive T-cell therapy; CAR T-cell; Neuroimmunology; adverse events; drug safety.

Publication types

  • Review

MeSH terms

  • Cell- and Tissue-Based Therapy
  • Cytokine Release Syndrome
  • Humans
  • Immunotherapy, Adoptive / adverse effects
  • Neurotoxicity Syndromes* / etiology
  • Receptors, Antigen, T-Cell
  • Receptors, Chimeric Antigen*

Substances

  • Receptors, Chimeric Antigen
  • cell-associated neurotoxicity
  • Receptors, Antigen, T-Cell