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Updated: May 29, 2026

Nerve Excitability Assessment in Chemotherapy-induced Neurotoxicity
Published on: April 26, 2012
Chemotherapy-induced peripheral neurotoxicity (CIPN): an update
Andreas A Argyriou1, Jordi Bruna, Paola Marmiroli
1Department of Neurology, Saint Andrew's General Hospital of Patras, Greece.
Peripheral neurotoxicity from chemotherapy drugs like platinum derivatives and antitubulins is a significant clinical issue. This review examines chemotherapy-induced peripheral neurotoxicity (CIPN) and emerging treatments.
Area of Science:
- Neuroscience
- Oncology
- Pharmacology
Background:
- The peripheral nervous system (PNS) is susceptible to drug toxicity due to limited protection.
- Drug-induced neurotoxicity can impact nerve fibers or neuronal bodies, particularly dorsal root ganglia.
- Antineoplastic agents are a major cause of neurotoxicity, often presenting as dose-limiting side effects.
Purpose of the Study:
- To review the features of chemotherapy-induced peripheral neurotoxicity (CIPN).
- To focus on neurotoxicity caused by platinum derivatives, antitubulins, thalidomide, and bortezomib.
- To highlight emerging antineoplastic agents like epothilones and proteasome inhibitors.
Main Methods:
- Literature review of drug-induced peripheral neurotoxicity.
- Analysis of clinical data on chemotherapy side effects.
- Focus on specific classes of antineoplastic agents.
Main Results:
- Antineoplastic agents frequently cause dose-limiting peripheral neurotoxicity.
- CIPN can severely impact cancer patients' quality of life and cause chronic discomfort.
- Platinum derivatives, antitubulins, thalidomide, and bortezomib are associated with severe PNS effects.
Conclusions:
- Chemotherapy-induced peripheral neurotoxicity is a critical clinical challenge.
- Understanding CIPN is essential for managing cancer patient care.
- Newer agents like epothilones and proteasome inhibitors require further investigation for their neurotoxic potential.
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