Neurological Adverse Effects of Immune Checkpoint Inhibitors and Chimeric Antigen Receptor T-Cell Therapy
Farhan Khalid1, Rajshree Gupta2, Rajvi Gor3
1Department of Medicine, Monmouth Medical Center, Long Branch, NJ 07740, USA.
Abstract:
Immune checkpoint inhibitors (ICPIs) and chimeric antigen receptor (CAR) T-cell constitute recently approved novel therapies targeted to treat a wide number of malignancies. Both the treatments modulate the immune system and can cause a number of immune-related adverse events (irAEs), including polyendocrinopathies, gastrointestinal and neurological complications. This literature review focuses on the neurological side effects of these therapies as these are uncommon and alter the course of the treatment. Neurological complications involve the peripheral and central nervous system, including polyneuropathy, myositis, myasthenia gravis, demyelinating polyradiculopathy, myelitis, and encephalitis. If early recognized, the neurological complications can be treated effectively with steroids to reduce the potential of short-term and long-term complications. Therefore, early identification and treatment of irAEs are needed to optimize the outcomes associated with ICPI and CAR T-cell therapies.
Insights
Novel cancer therapies like immune checkpoint inhibitors (ICPIs) and chimeric antigen receptor (CAR) T-cell therapy can cause rare but serious neurological side effects. Early recognition and steroid treatment are crucial for managing these immune-related adverse events (irAEs).
Area of Science:
- Oncology
- Immunology
- Neurology
Background:
- Immune checkpoint inhibitors (ICPIs) and chimeric antigen receptor (CAR) T-cell therapies are novel treatments for various cancers.
- These immunotherapies modulate the immune system, leading to potential immune-related adverse events (irAEs).
- Neurological complications are uncommon but can significantly impact treatment course and patient outcomes.
Purpose of the Study:
- To review the neurological side effects associated with ICPIs and CAR T-cell therapies.
- To highlight the spectrum of central and peripheral nervous system complications.
- To emphasize the importance of early diagnosis and management of these irAEs.
Main Methods:
- Literature review of neurological complications from ICPIs and CAR T-cell therapies.
- Analysis of reported cases involving peripheral and central nervous system involvement.
- Synthesis of current understanding of irAEs in neuro-oncology and immunotherapy.
Main Results:
- Neurological irAEs include polyneuropathy, myositis, myasthenia gravis, demyelinating polyradiculopathy, myelitis, and encephalitis.
- These complications affect both the peripheral and central nervous systems.
- Prompt recognition and treatment with steroids can mitigate short-term and long-term adverse effects.
Conclusions:
- Neurological irAEs are a critical consideration in patients receiving ICPIs and CAR T-cell therapies.
- Early identification and intervention with corticosteroids are essential for managing neurotoxicity.
- Optimizing patient outcomes requires vigilant monitoring and timely management of these immune-related neurological events.
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