Cytokine release syndrome. Reviewing a new entity in the intensive care unit

Med Intensiva (Engl Ed). 2019 Nov;43(8):480-488. doi: 10.1016/j.medin.2019.01.009. Epub 2019 Mar 25.
[Article in English, Spanish]

Abstract

Immunotherapy seeks to harness the power of the immune system to eradicate malignant tissues. Despite impressive therapeutic success, however, it can be accompanied by severe adverse effects such as cytokine release syndrome (CRS). These therapies cause the release of a great amount of cytokines, with IL-6 playing a central role, that can potentially lead to multiple organ dysfunction. The diagnosis is based on the presence of compatible clinical symptoms, elevated biomarkers and recent treatment with a biological agent. Mild cases can be managed through symptomatic treatment and fluids, while more severe episodes may need supportive therapy and specific care with the anti-IL-6 receptor monoclonal antibody tocilizumab. Although corticosteroids are also effective, they suppress T-cell activity, and so should only be considered as second line therapy or in cases of severe neurological involvement, since tocilizumab does not cross the blood-brain barrier. Cytokine release syndrome generally has a good prognosis, often being reversible and with a good response to specific treatment. Despite possible concerns about the admission of such patients (mainly with advanced oncological disease), we consider that the Intensive Care Unit should remain an option, since these individuals present a potentially reversible drug-related adverse event and are being treated with a new drug that could change the prognosis of the disorder. Intensive care medicine will become a key component in the management of the complications of modern cancer therapies, dealing with patients presenting an overactive immune system producing organ dysfunction while also trying to maintain treatment efficacy. This is the new paradigm.

Keywords: Cancer; Cytokine release syndrome; Cáncer; Immunotherapy; Inmunoterapia; Síndrome de liberación de citocinas.

Publication types

  • Review

MeSH terms

  • Adrenal Cortex Hormones / therapeutic use
  • Antibodies, Monoclonal, Humanized / therapeutic use
  • Brain Diseases / drug therapy
  • Brain Diseases / etiology
  • Cytokine Release Syndrome* / diagnosis
  • Cytokine Release Syndrome* / drug therapy
  • Cytokine Release Syndrome* / etiology
  • Cytokines / metabolism
  • Humans
  • Immunotherapy, Adoptive / adverse effects*
  • Immunotherapy, Adoptive / methods
  • Intensive Care Units*
  • Interleukin-6 / antagonists & inhibitors
  • Interleukin-6 / metabolism*
  • Lymphohistiocytosis, Hemophagocytic / genetics
  • Neoplasms / therapy*
  • Prognosis
  • Receptors, Chimeric Antigen / therapeutic use
  • Symptom Assessment

Substances

  • Adrenal Cortex Hormones
  • Antibodies, Monoclonal, Humanized
  • Cytokines
  • Interleukin-6
  • Receptors, Chimeric Antigen
  • tocilizumab