Treatment of patients with cancer using PD‑1/PD‑L1 antibodies: Adverse effects and management strategies (Review)

Int J Oncol. 2022 Jun;60(6):74. doi: 10.3892/ijo.2022.5364. Epub 2022 Apr 29.

Abstract

In 2020, there were an estimated 19.3 million new cancer cases and close to 10 million cancer deaths worldwide. Cancer remains one of the leading causes of death. In recent years, with the continuous improvement of our understanding of tumor immunotherapy, immunotherapeutics, such as immune checkpoint inhibitors, have gradually become a hot spot for tumor treatment. Amongst these, programmed cell death protein 1/programmed cell death protein ligand 1 (PD‑1/PD‑L1) related inhibitors, such as nivolumab and pembrolizumab, atezolizumab, avelumab and durvalumab have been shown to exhibit a high level of efficacy in several types of tumors. It has been confirmed that these inhibitors play an important role in the anti‑tumor process, significantly improving the survival rate of patients and delaying the progress of the underlying cancer. However, its method of therapeutic interference and potential for damaging the immune system has caused concern regarding its suitability. As these adverse effects are caused by an immune response to endogenous tissues, they are designated as immune‑related adverse events (irAEs). In this review, the typical irAEs reported in recent years and the management strategies adopted are highlighted, to serve as a reference in assessing the clinical response to these adverse reactions.

Keywords: adverse effects; cancer; immune‑related adverse events; immune‑therapy; programmed cell death protein 1; programmed cell death protein ligand 1.

Publication types

  • Review

MeSH terms

  • B7-H1 Antigen*
  • Humans
  • Immunotherapy / adverse effects
  • Neoplasms* / etiology
  • Neoplasms* / therapy
  • Programmed Cell Death 1 Receptor
  • Survival Rate

Substances

  • B7-H1 Antigen
  • Programmed Cell Death 1 Receptor

Grants and funding

No funding was received.