Extracorporeal cytokine removal in severe CAR-T cell associated cytokine release syndrome

J Crit Care. 2020 Jun:57:124-129. doi: 10.1016/j.jcrc.2020.02.010. Epub 2020 Feb 19.

Abstract

Purpose: Life-threatening complications of CD-19 Chimeric antigen receptor - T (CAR-T) cells such as the cytokine release syndrome (CRS)) have been reported. Treatment is limited to IL-6 blockade and steroids although global removal of elevated soluble inflammatory factors might be more effective.

Methods: Clinical course of a CRS patient treated with extracorporeal cytokine adsorption (Cytosorb®). A panel of 48 cytokines, chemokines and endothelial markers has been analyzed longitudinally. Ex vivo stimulation of endothelial cells to visualize (immunocytochemistry) and quantify (ECIS, TER) endothelial barrier effects.

Results: Following CAR-T cell application a 65 years old male developed grade 4 CRS with refractory shock (3 vasopressors) and severe capillary leakage (+37 L/24 h resuscitation). Treatment included IL-6 blockade, methylprednisolone and additionally Cytosorb hemoperfusion. While multiple soluble inflammatory factors were elevated and most of them decreased by more than 50% following Cytosorb, markers of endothelial injury increased steadily (e.g. Angpt-2/Angpt-1) leading to profound endothelial activation and leakage in ex vivo assays.

Conclusion: This is the first reported use of cytokine adsorption for CRS showing efficacy in absorption of various cytokines but not endothelial growth factors. A randomized controlled trial to evaluate additional Cytosorb treatment in CRS is currently recruiting at our institution (NCT04048434).

Keywords: CAR-T-cell; Cytokine release syndrome; Extracorporeal cytokine adsorption.

Publication types

  • Case Reports

MeSH terms

  • Adsorption
  • Cytokine Release Syndrome / etiology
  • Cytokine Release Syndrome / immunology*
  • Cytokines / immunology*
  • Endothelial Cells / metabolism
  • Hemoperfusion
  • Humans
  • Immunohistochemistry
  • Immunotherapy, Adoptive / adverse effects*
  • Interleukin-6 / metabolism
  • Longitudinal Studies
  • Male
  • Middle Aged
  • Receptors, Antigen, T-Cell / immunology
  • Receptors, Chimeric Antigen / immunology*
  • Receptors, Chimeric Antigen / therapeutic use
  • T-Lymphocytes / immunology
  • Treatment Outcome

Substances

  • Cytokines
  • IL6 protein, human
  • Interleukin-6
  • Receptors, Antigen, T-Cell
  • Receptors, Chimeric Antigen

Associated data

  • ClinicalTrials.gov/NCT04048434