Immune checkpoint inhibitors and elderly people: A review

Eur J Cancer. 2017 Sep:82:155-166. doi: 10.1016/j.ejca.2017.05.044. Epub 2017 Jul 6.

Abstract

Immune checkpoint inhibitors, including targeting programmed cell death 1, programmed cell death ligand 1, and cytotoxic T lymphocyte antigen 4 pathways, are a new type of cancer treatment. This approach of targeting the immune system has demonstrated dramatic efficacy for several cancers, and various drugs have been approved by health authorities and are used in clinical practice. Elderly patients (≥65 years) represent most of the cancers diagnosed and deaths by age group, with an increase expected over the next decade. However, this subgroup of patients is under-represented in clinical trials. Ageing is also associated with a decrease in the effectiveness of the immune system and in alterations to it. Few specific trials have been carried out for immunotherapy in elderly people, with most patients considered to be fit. In this review, we discuss the impact of ageing and immunosenescence on immune system functions, and we assess the safety and efficacy of immune checkpoint inhibitors in elderly patients, principally from the data of pivotal clinical trials with subgroup analysis. Tolerance in elderly patients seems similar to younger people, but efficacy seems different between younger and elderly patients according to the type of cancer, some showing no difference and others less efficacy in the elderly subgroup. However, the numbers in elderly groups are small and more investigation is needed, with specific clinical trials for elderly cancer patients.

Keywords: Adverse events; Elderly people; Immune checkpoint inhibitors.

Publication types

  • Review

MeSH terms

  • Aged
  • Aging / physiology*
  • Antineoplastic Agents / adverse effects*
  • Clinical Trials as Topic
  • Humans
  • Immunity, Innate / drug effects
  • Immunity, Innate / physiology*
  • Immunotherapy / adverse effects*
  • Neoplasms / drug therapy*
  • Neoplasms / immunology
  • T-Lymphocytes / immunology
  • Tumor Microenvironment / immunology

Substances

  • Antineoplastic Agents