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Updated: Mar 17, 2026

Nerve Excitability Assessment in Chemotherapy-induced Neurotoxicity
Published on: April 26, 2012
Chemotherapy-Related Neurotoxicity
Sophie Taillibert1, Emilie Le Rhun2,3,4, Marc C Chamberlain5
1Department of Neurology 2. Pitié-Salpétrière Hospital, Assistance Publique des Hôpitaux de Paris (APHP), University Pierre and Marie Curie, Paris VI, Paris, France.
Chemotherapy can harm the nervous system, causing central and peripheral neurotoxicity. Chemotherapy-induced peripheral neuropathy (CIPN) is common, with duloxetine showing promise for symptom management.
Area of Science:
- Neuroscience
- Oncology
- Pharmacology
Background:
- Chemotherapy can cause significant neurotoxicity affecting both central and peripheral nervous systems.
- Manifestations range from encephalopathies and cognitive impairment to peripheral neuropathy and myopathy.
- Chemotherapy-induced peripheral neuropathy (CIPN) is a prevalent complication, often presenting as sensory axonopathy.
Purpose of the Study:
- To review the spectrum of neurotoxic effects of chemotherapy.
- To discuss the clinical presentation and management of chemotherapy-induced neurotoxicity.
- To highlight CIPN as a common and challenging side effect.
Main Methods:
- Literature review of chemotherapy-induced neurotoxicity.
- Analysis of clinical syndromes affecting the central and peripheral nervous systems.
- Evaluation of treatment options for CIPN.
Main Results:
- Central neurotoxicity presents with diverse syndromes like encephalopathies and cognitive deficits.
- Peripheral neurotoxicity includes CIPN, the most frequent complication, and chemotherapy-induced myopathy.
- Duloxetine is identified as a preferred symptomatic treatment for CIPN based on meta-analysis.
Conclusions:
- Chemotherapy poses risks to both central and peripheral nervous systems.
- CIPN is a dose-dependent, length-dependent sensory axonopathy requiring careful management.
- Effective treatments for CIPN are limited, with duloxetine offering symptomatic relief.
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