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Journal ArticleDOI

Chemotherapy-induced neuropathy.

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TLDR
The neurologist managing the cancer patient who develops neuropathy must answer a series of important questions as follows: Are the symptoms due to peripheral neuropathy?
Abstract
Neurotoxic side effects of cancer therapy are second in frequency to hematological toxicity. Unlike hematological side effects that can be treated with hematopoietic growth factors, neuropathies cannot be treated and protective treatment strategies have not been effective. For the neurologist, the diagnosis of a toxic neuropathy is primarily based on the case history, the clinical and electrophysiological findings, and knowledge of the pattern of neuropathy associated with specific agents. In most cases, toxic neuropathies are length-dependent, sensory, or sensorimotor neuropathies often associated with pain. The platinum compounds are unique in producing a sensory ganglionopathy. Neurotoxicity is usually dependent on cumulative dose. Severity of neuropathy increases with duration of treatment and progression stops once drug treatment is completed. The platinum compounds are an exception where sensory loss may progress for several months after cessation of treatment ("coasting"). As more effective multiple drug combinations are used, patients will be treated with several neurotoxic drugs. Synergistic neurotoxicity has not been extensively investigated. Pre-existent neuropathy may influence the development of a toxic neuropathy. Underlying inherited or inflammatory neuropathies may predispose patients to developing very severe toxic neuropathies. Other factors such as focal radiotherapy or intrathecal administration may enhance neurotoxicity. The neurologist managing the cancer patient who develops neuropathy must answer a series of important questions as follows: (1) Are the symptoms due to peripheral neuropathy? (2) Is the neuropathy due to the underlying disease or the treatment? (3) Should treatment be modified or stopped because of the neuropathy? (4) What is the best supportive care in terms of pain management or physical therapy for each patient? Prevention of toxic neuropathies is most important. In patients with neuropathy, restorative approaches have not been well established. Symptomatic and other management are necessary to maintain and improve quality of life.

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Chemotherapy-induced peripheral neuropathy: Prevention and treatment strategies

TL;DR: New evidence strongly suggests that intravenous calcium and magnesium therapy can attenuate the development of oxaliplatin-induced CIPN, without reducing treatment response, and accumulating data suggest that vitamin E may also attenuateThe development of CIPn.
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Platinum neurotoxicity pharmacogenetics

TL;DR: Findings from the current literature for genetic markers associated with neurotoxicity induced by single-agent and combination platinum chemotherapy have the potential for broad clinical implications if mechanistic associations lead to the development of toxicity modulators to minimize the noxious sequelae of platinum chemotherapy.
Journal ArticleDOI

Chemotherapy-induced peripheral neurotoxicity (CIPN): An update

TL;DR: The features of chemotherapy-induced peripheral neurotoxicity (CIPN) resulting from the administration of these drugs are reviewed with a focus on new classes of promising antineoplastic agents, such as epothilones and proteasome inhibitors.
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Bortezomib-induced peripheral neuropathy in multiple myeloma: a comprehensive review of the literature

TL;DR: It is increasingly recognized that BIPN may be a proteasome inhibitor class effect, producing primarily a small fiber and painful, axonal, sensory distal neuropathy.
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Peripheral neuropathies from chemotherapeutics and targeted agents: diagnosis, treatment, and prevention

TL;DR: Peripheral neuropathies induced by chemotherapy (CIPN) are an increasingly frequent problem, and concepts of rehabilitation need to be implemented to improve the patients' functions and quality of life.
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Journal ArticleDOI

A Practical Two-Step Quantitative Clinical and Electrophysiological Assessment for the Diagnosis and Staging of Diabetic Neuropathy

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