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Immune Checkpoint Inhibitor-associated Diarrhea and Colitis: A Systematic Review and Meta-analysis of Observational
Ashley N Tran1, Melinda Wang1, Melanie Hundt2
1Section of Digestive Diseases.
Immune checkpoint inhibitor (ICI) therapy can cause diarrhea and colitis, affecting over 10% of patients. Combination therapy with corticosteroids and biologics improves remission rates for these side effects.
Area of Science:
- Oncology
- Immunology
- Gastroenterology
Background:
- Immune checkpoint inhibitors (ICIs) have revolutionized advanced cancer treatment.
- Diarrhea and colitis are significant side effects of ICI therapy.
- Understanding the incidence and outcomes of these gastrointestinal toxicities is crucial for patient management.
Purpose of the Study:
- To systematically review and meta-analyze the incidence and outcomes of diarrhea and colitis associated with ICI therapy.
- To compare the incidence of these side effects between different types of ICIs.
- To evaluate the effectiveness of different treatment strategies for ICI-induced diarrhea and colitis.
Main Methods:
- Systematic review and meta-analysis of observational studies.
- Searched bibliographic databases up to August 13, 2019.
- Included 25 studies with 12,661 patients, analyzing incidence, treatment, and outcomes.
- Employed random-effects models for meta-analyses.
Main Results:
- Overall incidence of diarrhea/colitis was 12.8%, higher with anti-cytotoxic T-cell lymphocyte-associated antigen 4 (20.1%) than anti-programmed cell death 1/programmed death-ligand 1 (4.1%).
- Remission rates were higher with corticosteroids plus biologics (88.4%) compared to corticosteroids alone (58.3%).
- Permanent ICI discontinuation occurred in 48.1% of patients; 48.6% resumed therapy with a 17.0% recurrence rate.
Conclusions:
- Real-world incidence of ICI-associated diarrhea/colitis exceeds 10%, leading to permanent discontinuation in over 50% of cases.
- Combination therapy with corticosteroids and biologics significantly improves remission.
- Further research is needed to guide early biologic treatment and safe resumption of ICI therapy.
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