Literature DB >> 17992096

Neurologic complications of chemotherapy agents.

George Kannarkat1, Erin E Lasher, David Schiff.   

Abstract

PURPOSE OF REVIEW: To review neurologic complications of common and recently developed chemotherapeutic agents, as well as recent research regarding 'chemobrain'. RECENT
FINDINGS: Bortezomib, a new anticancer agent, has a propensity toward causing a largely sensory and reversible peripheral neuropathy. Infusion of magnesium and calcium pre and post-oxaliplatin infusion reduces neuropathy but may interfere with clinical response to oxaliplatin. No other measures currently reduce the incidence or severity of neuropathy related to platinum compounds, taxanes, or thalidomide. Chemobrain, cognitive decline attributed to chemotherapy, has garnered research interest. Prevalence and epidemiology of chemobrain are poorly understood. Potential underlying mechanisms are under investigation in animal models and include effects on long-term potentiation and cerebral blood flow. Blood-brain barrier permeability, efficiency of cellular efflux pumps, DNA damage, telomere shortening, alteration of cytokine regulation, defects in neural repair, and oxidative stress may play roles in the effects of chemotherapy on central nervous system function.
SUMMARY: Data on prevention and treatment of chemotherapy-induced peripheral neuropathy are limited. Calcium and magnesium infusions for oxaliplatin administration have the most scientific support and are widely used in practice but may interfere with the clinical efficacy of oxaliplatin. Some novel agents, particularly bortezomib, have significant risk of chemotherapy-induced peripheral neuropathy. Animal models are beginning to reveal the mechanisms underlying the impact of individual chemotherapeutic drugs on cognition.

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Year:  2007        PMID: 17992096     DOI: 10.1097/WCO.0b013e3282f1a06e

Source DB:  PubMed          Journal:  Curr Opin Neurol        ISSN: 1350-7540            Impact factor:   5.710


  50 in total

1.  Chemotherapy-induced peripheral neuropathy, physical activity and health-related quality of life among colorectal cancer survivors from the PROFILES registry.

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2.  Inhibitors of histone deacetylases enhance neurotoxicity of DNA damage.

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3.  Chemotherapy-Induced Peripheral Neuropathy in Pediatric Cancer Patients.

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Review 4.  Cannabinoids: Current and Future Options to Treat Chronic and Chemotherapy-Induced Neuropathic Pain.

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Journal:  Drugs       Date:  2019-06       Impact factor: 9.546

5.  CD8+ T Cells and Endogenous IL-10 Are Required for Resolution of Chemotherapy-Induced Neuropathic Pain.

Authors:  Karen Krukowski; Niels Eijkelkamp; Geoffroy Laumet; C Erik Hack; Yan Li; Patrick M Dougherty; Cobi J Heijnen; Annemieke Kavelaars
Journal:  J Neurosci       Date:  2016-10-26       Impact factor: 6.167

6.  Comparison of oxaliplatin- and cisplatin-induced painful peripheral neuropathy in the rat.

Authors:  Elizabeth K Joseph; Jon D Levine
Journal:  J Pain       Date:  2009-02-23       Impact factor: 5.820

Review 7.  Animal models of chemotherapy-evoked painful peripheral neuropathies.

Authors:  Nicolas Authier; David Balayssac; Fabien Marchand; Bing Ling; Aude Zangarelli; Juliette Descoeur; François Coudore; Emmanuel Bourinet; Alain Eschalier
Journal:  Neurotherapeutics       Date:  2009-10       Impact factor: 7.620

Review 8.  Cancer pain: perspectives of a medical oncologist.

Authors:  Keith D Eaton; Deborah A Frieze
Journal:  Curr Pain Headache Rep       Date:  2008-08

Review 9.  DNA damage response in peripheral nervous system: coping with cancer therapy-induced DNA lesions.

Authors:  Ella W Englander
Journal:  DNA Repair (Amst)       Date:  2013-05-16

10.  Confronting chemobrain: an in-depth look at survivors' reports of impact on work, social networks, and health care response.

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Journal:  J Cancer Surviv       Date:  2009-09-16       Impact factor: 4.442

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