The Journal of Community and Supportive Oncology · 2015 · 12 citations · 6 references
MedicineOncologyPharmacologyCancer PharmacologyChemotherapyNeuro-oncologyAdverse Effects Of ChemotherapyNeuropathic PainPeripheral Nervous System ToxicityPeripheral Neuropathy ManagementAnticonvulsant ActionAnticonvulsant DrugsChemotherapy Dose-limiting ToxicityDrug DiscontinuationDrug-induced Peripheral NeuropathyPeripheral Neuropathy PharmacotherapyVoltage-gated ChannelsVoltage-gated Sodium Channels
Chemotherapy-induced peripheral neuropathy (CIPN) is a major dose-limiting toxicity of potentially curative cancer therapy regimens. Cisplatin is the class of chemotherapy agent that has a broad spectrum of activity against several solid tumors, but it induces sensory neuropathy of upper and lower extremities. Cisplatin-induced peripheral neuropathy is usually in a "gloves and socks" distribution that can persist for months or years after completion of chemotherapy treatment. If the pain is severe, it affects the patient's long-term quality of life and can potentially result in chemotherapy dose reduction or treatment discontinuation. The mechanism of CIPN is not well understood, and a number of pathophysiological mechanisms have been proposed to explain the phenomenon. Although many therapies have been investigated for the prevention or treatment of CIPN, there is currently no accepted proven therapy. Here we report a case in which lacosamide alleviated painful CIPN symptoms. Lacosamide is an anticonvulsant drug that blocks the voltage-gated sodium channels in the neurons and may also be a promising novel candidate for the prevention and treatment of chemotherapy-induced peripheral neuropathy. Preclinical data support the role of lacosamide protective effect in a rat model of chemotherapy-induced neuropathy, randomized clinical trial is needed.
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Lacosamide in Painful Diabetic Peripheral Neuropathy
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Role of pregabalin in treatment of oxaliplatin-induced sensory neuropathy.
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Examining the Clinical Utility of Lacosamide
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