Literature DB >> 30922608

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

Alejandra García Roche1, Cándido Díaz Lagares2, Elena Élez3, Ricard Ferrer Roca1.   

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.
Copyright © 2019 Elsevier España, S.L.U. and SEMICYUC. All rights reserved.

Entities:  

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

Mesh:

Substances:

Year:  2019        PMID: 30922608     DOI: 10.1016/j.medin.2019.01.009

Source DB:  PubMed          Journal:  Med Intensiva (Engl Ed)        ISSN: 2173-5727


  4 in total

1.  Anti-inflammatory and immune-mediated therapy for a case of febrile infection-related epilepsy syndrome with rapid recurrence.

Authors:  Tomonori Kurimoto; Tsuyoshi Matsuoka; Yuki Ami; Koji Kanno; Takashi Fujii; Naoki Fujiwara; Takashi Matsuoka
Journal:  Clin Case Rep       Date:  2022-06-07

2.  Preclinical safety evaluation of chimeric antigen receptor-modified T cells against CD19 in NSG mice.

Authors:  Hairuo Wen; Zhe Qu; Yujing Yan; Chengfei Pu; Chao Wang; Hua Jiang; Tiantian Hou; Yan Huo
Journal:  Ann Transl Med       Date:  2019-12

Review 3.  Diseases with health disparities as drivers of COVID-19 outcome.

Authors:  John T Moore; William Pilkington; Deepak Kumar
Journal:  J Cell Mol Med       Date:  2020-08-20       Impact factor: 5.310

Review 4.  Intestinal permeability changes with bacterial translocation as key events modulating systemic host immune response to SARS-CoV-2: A working hypothesis.

Authors:  Vincenzo Cardinale; Gabriele Capurso; Gianluca Ianiro; Antonio Gasbarrini; Paolo Giorgio Arcidiacono; Domenico Alvaro
Journal:  Dig Liver Dis       Date:  2020-09-16       Impact factor: 4.088

  4 in total

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