Programmed Cell Death Protein 1 Inhibitor-Mediated Peripheral Neuropathy
Yanyun Ao1, Ming Gao2, Binbin Sun2
1First Medical Center of PLA General Hospital, Beijing, People's Republic of China.
JTO Clinical and Research Reports
|April 25, 2023
Summary
Immune checkpoint inhibitors (ICIs) treat cancer but can cause rare, severe neurologic side effects like peripheral neuropathy. This review summarizes PD-1 inhibitor neurotoxicity to improve clinical awareness and patient outcomes.
Area of Science:
- Oncology
- Immunology
- Neuroscience
Background:
- Immune checkpoint inhibitors (ICIs) have transformed cancer treatment by harnessing the immune system.
- Common ICIs include programmed cell death protein 1 (PD-1) and cytotoxic T lymphocyte-associated protein 4 (CTLA-4) inhibitors.
- While effective, ICIs can cause immune-related adverse events affecting various organ systems.
Purpose of the Study:
- To report cases of peripheral neuropathy associated with PD-1 inhibitor therapy.
- To review and summarize neurotoxicity induced by PD-1 inhibitors from existing literature.
- To enhance clinician and patient awareness of these rare but serious neurologic adverse reactions.
Main Methods:
- Case reporting of peripheral neuropathy in patients treated with PD-1 inhibitors.
- Comprehensive literature search for studies on PD-1 inhibitor-induced neurotoxicity.
- Synthesis of findings to characterize the neurotoxic effects and their management.
Main Results:
- Peripheral neuropathy is a rare but significant adverse event associated with PD-1 inhibitors.
- Neurotoxicity can severely impact patient quality of life and prognosis.
- Understanding the spectrum of neurotoxicity is crucial for timely diagnosis and intervention.
Conclusions:
- PD-1 inhibitors, despite their therapeutic benefits, carry a risk of neurologic toxicity, including peripheral neuropathy.
- Increased clinical vigilance and patient education are essential for managing these adverse events.
- Further research may elucidate mechanisms and improve strategies to mitigate ICI-related neurotoxicity.
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