Language

English

Publication Date

11-1-2025

Journal

Immunotherapy

DOI

10.1080/1750743X.2025.2600847

PMID

41367243

PMCID

PMC12952247

PubMedCentral® Posted Date

12-10-2025

PubMedCentral® Full Text Version

Post-print

Abstract

Background: Immune checkpoint inhibitors (ICIs) are pivotal in systemic anticancer therapy. The aim of the study was to investigate incidence, severity and consequences of immune-related adverse events (irAEs) in ICI combinations by comparing different adverse events classification systems.

Methods: A retrospective multicentre cohort study included patients treated with ICI combinations. IrAEs were assessed by CTCAE v.5, NCC MERP index and SITC consensus for chronic irAEs.

Results: Among 612 patients, 244 (40%) experienced 354 irAEs, in total 58 irAEs per 100 patients varying between treatments. Higher incidence was observed for autoimmune disease, thoracic radiotherapy, melanoma, dual ICI and ICI/TKI. Severe irAEs occurred in 147 patients, leading to treatment discontinuation and hospitalization in half of the patients. Chronic irAEs were common, with 64% persisting beyond three months after ICI discontinuation, 22% of these resolved (median 135 steroid days, 154 days to resolution). Common chronic toxicities included endocrine, pulmonary or rheumatic irAEs. Fatal irAEs affected 16 patients, primarily from pneumonitis, colitis or hepatitis.

Conclusion: NCC MERP better captured clinical consequences compared to CTCAE, while SITC criteria uniquely identified long-term irAEs. Severe and chronic irAEs were frequent, emphasizing the need for improved communication about irAE management and prospective studies with revised toxicity definitions.ClinicalTrials.govIDNCT06476158.

Keywords

Humans, Male, Female, Neoplasms, Immune Checkpoint Inhibitors, Retrospective Studies, Aged, Middle Aged, Immunotherapy, Adult, Aged, 80 and over, Drug-Related Side Effects and Adverse Reactions, Incidence, irAE, immunotherapy combinations, NCC MERP, CTCAE, chronic, long-term, SITC, consequences

Published Open-Access

yes

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