Genetic determinants of taxane-induced peripheral neuropathy

Bratisl Lek Listy. 2024;125(4):207-210. doi: 10.4149/BLL_2024_31.

Abstract

The efficacy of taxane‑containing regimens has been demonstrated for various cancers, particularly ovarian, endometrial, breast, lung, and prostate cancers. However, extensive taxane-induced toxicities limit their use. Prediction and management of many toxic complications in cancer patients have evolved significantly over the last decade. Peripheral neuropathy is the most typical non-hematological taxane-related complication, and it has a multifactorial pathogenesis. It is often dose-dependent and progressive during therapy and sometimes even after treatment. Unfortunately, the prediction of these common adverse events remains unclear. In the past few years, several polymorphisms of candidate genes with a possible role in the development of this consequence were studied. This minireview aims to highlight the critical yet underappreciated roles of genetic predictors that may increase susceptibility to taxane-induced peripheral neuropathy in cancer patients (Ref. 40). Keywords: taxanes, paclitaxel, docetaxel, peripheral neuropathy, risk factors, genetic polymorphisms.

MeSH terms

  • Breast Neoplasms*
  • Bridged-Ring Compounds*
  • Humans
  • Male
  • Paclitaxel / adverse effects
  • Peripheral Nervous System Diseases* / chemically induced
  • Peripheral Nervous System Diseases* / genetics
  • Prostatic Neoplasms*
  • Taxoids / adverse effects

Substances

  • taxane
  • Taxoids
  • Paclitaxel
  • Bridged-Ring Compounds