Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2021 Oct;18(4):2384-2396.
doi: 10.1007/s13311-021-01142-2. Epub 2021 Oct 21.

Chemotherapy-Induced Peripheral Neuropathy: Mechanisms and Therapeutic Avenues

Affiliations
Review

Chemotherapy-Induced Peripheral Neuropathy: Mechanisms and Therapeutic Avenues

Esther H Bae et al. Neurotherapeutics. 2021 Oct.

Abstract

Chemotherapy-induced peripheral neuropathy (CIPN) is a serious and often persistent adverse consequence of certain chemotherapeutic agents. It is a major dose-limiting factor of many first-line chemotherapies, affecting 20-50% of patients at standard doses and nearly all patients at high doses. As cancer survivorship continues to increase with improvements in early diagnosis and treatment, more patients will experience CIPN despite completing cancer treatment, which interferes with recovery, leading to chronic pain and worsening quality of life. The National Cancer Institute has identified CIPN as a priority in translational research. To date, there are no FDA-approved drugs for preventing or treating CIPN, with emerging debate on mechanisms and promising new targets. This review highlights current literature and suggests novel approaches to CIPN based on proposed mechanisms of action that aim either to confer neuroprotection against chemotherapy-induced neurotoxicity or reverse the downstream effects of painful neuropathy.

Keywords: Antinociceptive; Chemotherapy-induced peripheral neuropathy; Mechanisms; Neuroprotective; Treatment.

PubMed Disclaimer

Conflict of interest statement

The authors declare no competing interests.

Similar articles

Cited by

References

    1. Quasthoff S, Hartung HP. Chemotherapy-induced peripheral neuropathy. J Neurol. 2002;249(1):9–17. doi: 10.1007/pl00007853. - DOI - PubMed
    1. Swain SM, Arezzo JC. Neuropathy associated with microtubule inhibitors: diagnosis, incidence, and management. Clin Adv Hematol Oncol. 2008;6(6):455–467. - PubMed
    1. Perez EA. Microtubule inhibitors: Differentiating tubulin-inhibiting agents based on mechanisms of action, clinical activity, and resistance. Mol Cancer Ther. 2009;8(8):2086–2095. doi: 10.1158/1535-7163.MCT-09-0366. - DOI - PubMed
    1. Shin GJ, Pero ME, Hammond LA, et al. Integrins protect sensory neurons in models of paclitaxel-induced peripheral sensory neuropathy. PNAS. 2021;118(15). 10.1073/pnas.2006050118 - PMC - PubMed
    1. Fukuda Y, Li Y, Segal RA. A mechanistic understanding of axon degeneration in chemotherapy-induced peripheral neuropathy. Front Neurosci. 2017;11:481. doi: 10.3389/fnins.2017.00481. - DOI - PMC - PubMed

MeSH terms

Substances