Abstract

Immune checkpoint inhibitors (ICI) are a novel class of antineoplastic treatment that enhances immunity against tumors. They are associated with immune adverse events, and several neurological syndromes have been described, including multiple sclerosis and atypical demyelination. We performed a systematic literature review of case reports with neurological immune adverse events that presented with central nervous system demyelination, up to December 2019. We found 23 cases: seven with myelitis, four isolated optic neuritis, one neuromyelitis optica spectrum disorder, five multiple sclerosis, and six with atypical demyelination. Ipilimumab was the most frequently used ICI (11/23). The median time to develop symptoms from the onset of ICI was 6.5 weeks [range 1.0–43.0], and from last ICI dose was 14 days [range 0–161]. Anatomopathological examination was performed in four cases, with the finding of a T-cell mediated immune response. Outcomes were generally favorable after immunosuppression: 18 patients had improvement or a full recovery, three patients did not respond to treatment, three patients died, and in one, treatment was not reported. We describe the patients' clinical presentation, treatment administered, and outcomes. We further speculate on possible pathophysiological mechanisms and discuss potential treatments that may be worth investigating.

Highlights

  • Immune checkpoint inhibitor (ICI) is a novel class of antineoplastic drugs that enhance antitumor immune responses through the upregulation of T cell activity

  • Articles included in this review contained 23 case reports of patients who developed central nervous system (CNS) demyelination after Immune checkpoint inhibitors (ICI) administration

  • Demyelination is a rare complication of ICI treatment

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Summary

Introduction

Immune checkpoint inhibitor (ICI) is a novel class of antineoplastic drugs that enhance antitumor immune responses through the upregulation of T cell activity. Their mechanism consists of blocking receptors that normally inhibit the T cell response, the so-called inhibitory immune checkpoints. The main targets of these medications are cytotoxic T lymphocyte antigen 4 (CTLA-4) receptor, programmed cell death 1 (PD-1) receptor, and programmed cell death 1 ligand (PD-L1) [1], which are molecules that break the T cell immune-mediated response. CTLA-4 is expressed on activated CD4+ T helper cells, regulatory T cells, and CD8+ cytotoxic T lymphocytes; they bind to its ligands, CD80 and CD86, expressed on professional antigen-presenting cells (APCs) [2]. Specific monoclonal antibodies that block the inhibitory action of these checkpoint molecules lead to persistent and generalized activation of the humoral and cellular adaptative immune system, enhancing antitumor immunity [4]

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