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.

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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