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Updated: Feb 7, 2026

Measuring Neuromuscular Junction Functionality
Published on: August 6, 2017
[Neuromuscular Adverse Events]
1Dept. of Neurology, Keio University School of Medicine.
Abstract:
Neuromuscular adverse events(AEs)associated with cancer treatment with immune checkpoint inhibitors(ICIs)include diverse clinical subsets. The general features of neuromuscular AEs have not been elucidated because the frequency is generally low, ranging from 1-2%of cancer patients undergoing ICIs therapy. The diseases affect the central nervous system, peripheral nerves, neuromuscular junction, and muscle. Disease onset and progression may be rapid with a critical clinical course. The clinical presentation may be different from that of patients unrelated to drugs. Headache, dizziness, and dysgeusia were relatively common and mild treatment-related AEs. In contrast, representative immune-related AEs such as autoimmune encephalitis, demyelinating polyneuropathy, myasthenia, and myositis were serious. There was a tight association between myasthenia, myositis, and myocarditis. There are guidelines for the treatment of neuromuscular immune-mediated AEs. For all but the minimum neurological symptoms, checkpoint inhibitor therapy should be withheld until the nature of the AEs is defined. Immune-modulating medication is generally effective for neuromuscular AEs. Both CD8+ cytotoxic T-cells and autoantibodies are involved in the pathogenesis of neuromuscular AEs. Correct understanding of neuromuscular AEs is required for the best management of cancer patients.
Insights
Immune checkpoint inhibitors (ICIs) can cause rare but serious neuromuscular adverse events (AEs) affecting the brain, nerves, and muscles. Early recognition and immune-modulating treatments are crucial for managing these potentially severe side effects in cancer patients.
Area of Science:
- Oncology
- Neurology
- Immunology
Background:
- Immune checkpoint inhibitors (ICIs) are revolutionary cancer therapies.
- Neuromuscular adverse events (AEs) are infrequent but serious complications of ICI treatment.
- The diverse clinical presentations and underlying mechanisms of ICI-related neuromuscular AEs require elucidation.
Purpose of the Study:
- To summarize the general features of neuromuscular AEs associated with ICIs.
- To highlight the spectrum of central nervous system, peripheral nerve, neuromuscular junction, and muscle involvement.
- To emphasize the importance of early diagnosis and management strategies for these AEs.
Main Methods:
- Review of clinical presentations and characteristics of neuromuscular AEs in cancer patients treated with ICIs.
- Analysis of the frequency, affected systems, and clinical course of these events.
- Discussion of the role of CD8+ cytotoxic T-cells and autoantibodies in pathogenesis.
Main Results:
- Neuromuscular AEs affect 1-2% of patients on ICIs, involving diverse neurological systems.
- Common mild AEs include headache, dizziness, and dysgeusia.
- Serious AEs include autoimmune encephalitis, demyelinating polyneuropathy, myasthenia gravis, and myositis, often associated with myocarditis.
Conclusions:
- Neuromuscular AEs from ICIs can have rapid onset and critical courses, differing from non-drug-related conditions.
- Withholding ICI therapy is recommended for significant neurological symptoms until diagnosis.
- Immune-modulating therapies are generally effective, and understanding pathogenesis is key for optimal patient management.
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