| Literature DB >> 28511129 |
Tejaswi Kandula1, Michelle A Farrar1, Matthew C Kiernan2, Arun V Krishnan3, David Goldstein3, Lisa Horvath4, Peter Grimison5, Frances Boyle6, Sally Baron-Hay7, Susanna B Park8.
Abstract
Chemotherapy induced peripheral neuropathy (CIPN) is a significant toxicity of cancer treatment, with the potential to affect long-term function and quality of life in cancer survivors. There remains a lack of consensus around optimal assessment techniques. While current approaches to CIPN assessment are focused on clinical grading scales, it is becoming increasingly evident that a more comprehensive multimodal assessment package is necessary to accurately characterise the impact of CIPN as well as gauge the utility of neuroprotective mechanisms. Neurophysiological techniques provide objective biomarkers and may enable early detection of toxicity while patient reported outcomes are necessary to determine the significance of symptoms to individual patients. In addition to providing an objective assessment, clinical neurophysiological techniques provide important insights into the contributory pathophysiological mechanisms of CIPN with different chemotherapy agents. There is a paucity of implementation of these techniques in the clinical trial setting. The present Review aims to facilitate the use of neurophysiological studies as part of comprehensive assessment packages for the monitoring of CIPN by summarising current understanding of neurophysiological changes that underlie the development of neuropathy, clinical presentations and patient reported outcomes as well as advantages and limitations of current techniques for the neurophysiological assessment of CIPN.Entities:
Keywords: Cancer late effects; Cancer survivorship; Chemotherapy induced peripheral neuropathy; Neurophysiology; Patient reported outcomes
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Year: 2017 PMID: 28511129 DOI: 10.1016/j.clinph.2017.04.009
Source DB: PubMed Journal: Clin Neurophysiol ISSN: 1388-2457 Impact factor: 3.708