Immune checkpoint inhibitor-induced diarrhea and colitis: an overview.


Journal

Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer
ISSN: 1433-7339
Titre abrégé: Support Care Cancer
Pays: Germany
ID NLM: 9302957

Informations de publication

Date de publication:
23 Sep 2024
Historique:
received: 13 05 2024
accepted: 17 09 2024
medline: 23 9 2024
pubmed: 23 9 2024
entrez: 23 9 2024
Statut: epublish

Résumé

Immune checkpoint inhibitors (ICIs) have emerged as an integral component of the management of various cancers and have contributed to significant improvements in overall survival. Most available ICIs target anti-cytotoxic T-lymphocyte-associated protein 4 (anti-CTLA4), and anti-programmed cell death 1/programmed cell death ligand 1 (anti-PD1/PDL1). Gastrointestinal immune-related adverse events remain a common complication of ICIs. The predominant manifestations include diarrhea and colitis, which often manifest concurrently as immune-mediated diarrhea and colitis (IMDC). Risk factors for developing these side effects include baseline gut microbiota, preexisting autoimmune disorders, such as inflammatory bowel disease, and type of neoplasm. The hallmark symptom of colitis is diarrhea which may be accompanied by mucus or blood in stools. Patients may also experience abdominal pain, fever, vomiting, and nausea. If not treated rapidly, ICI-induced colitis can lead to serious life-threatening complications. Current management is based on corticosteroids as first-line, and immunosuppressants like infliximab or vedolizumab for refractory cases. Microbiota transplantation and specific cytokines and lymphocyte replication inhibitors are being investigated. Optimal patient care requires maintaining a balance between treatment toxicity and efficacy, hence the aim of this review is to enhance readers' comprehension of the gastrointestinal adverse events associated with ICIs, particularly IMDC. In addition to identifying the risk factors, we discuss the incidence, clinical presentation, workup, and management options of IMDC.

Identifiants

pubmed: 39311981
doi: 10.1007/s00520-024-08889-2
pii: 10.1007/s00520-024-08889-2
doi:

Substances chimiques

Immune Checkpoint Inhibitors 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

680

Informations de copyright

© 2024. This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply.

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Auteurs

Marianne Zoghbi (M)

Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. mzoghbi@mdanderson.org.

Kathryn J Burk (KJ)

Department of Emergency Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Elio Haroun (E)

Faculty of Medicine, Saint Joseph University of Beirut, Beirut, 1100, Lebanon.

Maria Saade (M)

Faculty of Medicine, Saint Joseph University of Beirut, Beirut, 1100, Lebanon.

Maria Teresa Cruz Carreras (MTC)

Department of Emergency Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

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