Nephrotoxicity in cancer treatment: An update

Adv Cancer Res. 2022:155:77-129. doi: 10.1016/bs.acr.2022.03.005. Epub 2022 Apr 26.

Abstract

It has been estimated that nearly 80% of anticancer drug-treated patients receive potentially nephrotoxic drugs, while the kidneys play a central role in the excretion of anticancer drugs. Nephrotoxicity has long been a serious complication that hampers the effectiveness of cancer treatment and continues to influence both mortality and length of hospitalization among cancer patients exposed to either conventional cytotoxic agents or targeted therapies. Kidney injury arising from anticancer drugs tends to be associated with preexisting comorbidities, advanced cancer stage, and the use of concomitant non-chemotherapeutic nephrotoxic drugs. Despite the prevalence and impact of kidney injury on therapeutic outcomes, the field is sorely lacking in an understanding of the mechanisms driving cancer drug-induced renal pathophysiology, resulting in quite limited and largely ineffective management of anticancer drug-induced nephrotoxicity. Consequently, there is a clear imperative for understanding the basis for nephrotoxic manifestations of anticancer agents for the successful management of kidney injury by these drugs. This article provides an overview of current preclinical research on the nephrotoxicity of cancer treatments and highlights prospective approaches to mitigate cancer therapy-related renal toxicity.

Keywords: Chemotherapy; Immune checkpoint; Kidney toxicity; Non-coding RNAs; Risk factor; Sphingolipids; Targeted cancer therapy.

MeSH terms

  • Antineoplastic Agents* / adverse effects
  • Drug-Related Side Effects and Adverse Reactions*
  • Humans
  • Kidney
  • Neoplasms* / drug therapy
  • Prospective Studies

Substances

  • Antineoplastic Agents