Holistic Approach to Immune Checkpoint Inhibitor-Related Adverse Events.

PD-L1 cancer cytotoxic T lymphocyte-associated protein (CTLA-4) immune checkpoint inhibitor (ICI) immune-related adverse event (irAE) immunotherapy programmed cell death protein -1 (PD-1)

Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2022
Historique:
received: 29 10 2021
accepted: 07 03 2022
entrez: 18 4 2022
pubmed: 19 4 2022
medline: 20 4 2022
Statut: epublish

Résumé

Immune checkpoint inhibitors (ICIs) block inhibitory molecules, such as cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), programmed cell death protein 1 (PD-1), or its ligand, programmed cell death protein ligand 1 (PD-L1) and enhance antitumor T-cell activity. ICIs provide clinical benefits in a percentage of patients with advanced cancers, but they are usually associated with a remarkable spectrum of immune-related adverse events (irAEs) (e.g., rash, colitis, hepatitis, pneumonitis, endocrine, cardiac and musculoskeletal dysfunctions). Particularly patients on combination therapy (e.g., anti-CTLA-4 plus anti-PD-1/PD-L1) experience some form of irAEs. Different mechanisms have been postulated to explain these adverse events. Host factors such as genotype, gut microbiome and pre-existing autoimmune disorders may affect the risk of adverse events. Fatal ICI-related irAEs are due to myocarditis, colitis or pneumonitis. irAEs usually occur within the first months after ICI initiation but can develop as early as after the first dose to years after ICI initiation. Most irAEs resolve pharmacologically, but some appear to be persistent. Glucocorticoids represent the mainstay of management of irAEs, but other immunosuppressive drugs can be used to mitigate refractory irAEs. In the absence of specific trials, several guidelines, based on data from retrospective studies and expert consensus, have been published to guide the management of ICI-related irAEs.

Identifiants

pubmed: 35432346
doi: 10.3389/fimmu.2022.804597
pmc: PMC9005797
doi:

Substances chimiques

B7-H1 Antigen 0
Immune Checkpoint Inhibitors 0
Ligands 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

804597

Informations de copyright

Copyright © 2022 Poto, Troiani, Criscuolo, Marone, Ciardiello, Tocchetti and Varricchi.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Remo Poto (R)

Department of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.

Teresa Troiani (T)

Medical Oncology, Department of Precision Medicine, University of Campania Luigi Vanvitelli, Naples, Italy.

Gjada Criscuolo (G)

Department of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.
Center for Basic and Clinical Immunology Research (CISI), University of Naples Federico II, Naples, Italy.

Giancarlo Marone (G)

Moscati Hospital Pharmacy, Aversa, Italy.

Fortunato Ciardiello (F)

Medical Oncology, Department of Precision Medicine, University of Campania Luigi Vanvitelli, Naples, Italy.

Carlo Gabriele Tocchetti (CG)

Department of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.

Gilda Varricchi (G)

Department of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.
Center for Basic and Clinical Immunology Research (CISI), University of Naples Federico II, Naples, Italy.
World Allergy Organization (WAO) Center of Excellence, Naples, Italy.
Institute of Experimental Endocrinology and Oncology (IEOS), National Research Council, Naples, Italy.

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