Clinical Course and Impact of Immune Checkpoint Inhibitor Colitis Resembling Microscopic Colitis.

colitis drug-related side effects and adverse reactions immune checkpoint inhibitors inflammatory bowel diseases microscopic

Journal

Crohn's & colitis 360
ISSN: 2631-827X
Titre abrégé: Crohns Colitis 360
Pays: England
ID NLM: 101752188

Informations de publication

Date de publication:
Apr 2022
Historique:
received: 15 11 2021
entrez: 13 2 2023
pubmed: 14 2 2023
medline: 14 2 2023
Statut: epublish

Résumé

Microscopic colitis (MC) is suspected to result from increased immune activity in gut mucosa. Immune checkpoint inhibitors (ICIs) treat cancer by activating the immune system, and further investigation is needed regarding their role in the development of MC. A retrospective case series investigated cases of endoscopically and histologically confirmed MC developing after administration of ICIs. Clinical notes and medication administration records were reviewed for demographics, symptom duration, and treatment response. Nineteen cases of de novo MC were identified, with 95% of cases requiring steroid treatment, 53% presenting with hospitalization, and colitis-related mortality in 1 individual. Symptom onset occurred a median of 160 days after initiation of ICI therapy and 53 days after their most recent dose of therapy. Patients had a median of 125 days of symptoms, and ICI therapy was held in 70% of individuals due for treatment. MC can develop after ICI administration, and presents with severe symptoms, often requiring hospitalization and steroid treatment. In certain individuals this can require a prolonged treatment course of steroid therapy or immunomodulators. Individuals developing diarrhea after ICI therapy warrant thorough workup including endoscopy and rapid treatment initiation given the disease severity observed in this series.

Sections du résumé

Background UNASSIGNED
Microscopic colitis (MC) is suspected to result from increased immune activity in gut mucosa. Immune checkpoint inhibitors (ICIs) treat cancer by activating the immune system, and further investigation is needed regarding their role in the development of MC.
Methods UNASSIGNED
A retrospective case series investigated cases of endoscopically and histologically confirmed MC developing after administration of ICIs. Clinical notes and medication administration records were reviewed for demographics, symptom duration, and treatment response.
Results UNASSIGNED
Nineteen cases of de novo MC were identified, with 95% of cases requiring steroid treatment, 53% presenting with hospitalization, and colitis-related mortality in 1 individual. Symptom onset occurred a median of 160 days after initiation of ICI therapy and 53 days after their most recent dose of therapy. Patients had a median of 125 days of symptoms, and ICI therapy was held in 70% of individuals due for treatment.
Conclusions UNASSIGNED
MC can develop after ICI administration, and presents with severe symptoms, often requiring hospitalization and steroid treatment. In certain individuals this can require a prolonged treatment course of steroid therapy or immunomodulators. Individuals developing diarrhea after ICI therapy warrant thorough workup including endoscopy and rapid treatment initiation given the disease severity observed in this series.

Identifiants

pubmed: 36777041
doi: 10.1093/crocol/otac008
pii: otac008
pmc: PMC9802423
doi:

Types de publication

Journal Article

Langues

eng

Pagination

otac008

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of Crohn's & Colitis Foundation.

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Auteurs

Thomas W Fredrick (TW)

Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA.

Guilherme P Ramos (GP)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.

Manuel B Braga Neto (MB)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.

Sunanda Kane (S)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.

William A Faubion (WA)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.

Edward V Loftus (EV)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.

Darrell S Pardi (DS)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.

Shabana F Pasha (SF)

Division of Gastroenterology and Hepatology, Mayo Clinic, Phoenix, Arizona, USA.

Francis A Farraye (FA)

Division of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, Florida, USA.

Lizhi Zhang (L)

Division of Anatomic Pathology, Mayo Clinic, Rochester, Minnesota, USA.

Laura E Raffals (LE)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.

Classifications MeSH