Safety profile of immune checkpoint inhibitors according to cancer type

Chloé Guérin1, Mathieu Laramas2, François Bettega3

  • 1Grenoble Alpes University Hospital, Department of Internal Medicine/Clinical Immunology, Grenoble, France.

Bulletin Du Cancer
|May 24, 2023
PubMed
Abstract

Insights

Immune checkpoint inhibitors (ICI) can cause immune-related adverse events (irAEs). This study found ipilimumab and autoimmune disease history predict irAEs, while cancer type did not significantly influence their occurrence.

Area of Science:

  • Oncology
  • Immunology
  • Clinical Research

Background:

  • Immune checkpoint inhibitors (ICI) have transformed cancer therapy, introducing immune-related adverse events (irAEs).
  • Understanding predictive factors for irAEs is crucial for patient management and treatment optimization.

Purpose of the Study:

  • To investigate whether cancer type is a predictive factor for the occurrence of grade ≥2 immune-related adverse events (irAEs).
  • To identify patient and treatment-related factors associated with irAEs and irAEs-free survival.

Main Methods:

  • Retrospective analysis of 512 patients treated with ICI between 2019-2020.
  • Logistic regression and Fine and Gray survival models were employed to analyze associations with grade ≥2 irAEs and irAEs-free survival, considering death as a competing risk.

Main Results:

  • Grade ≥2 irAEs occurred in 31.2% of patients; they were less frequent in head and neck cancers.
  • Ipilimumab, longer treatment duration, and a history of autoimmune disease were independently associated with increased grade ≥2 irAEs.
  • Grade ≥2 irAEs-free survival was positively influenced by treatment duration, ipilimumab, and autoimmune disease history, but negatively by poor performance status and older age.

Conclusions:

  • Ipilimumab and a history of autoimmune disease are significant predictors of grade ≥2 irAEs and influence irAEs-free survival.
  • Cancer type was not found to be a significant predictive factor for irAEs in this cohort.

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