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Published on: December 16, 2021
Gastrointestinal Infection Before Immune Checkpoint Inhibition Hinders Treatment Efficacy and Increases the Risk of
Malek Shatila1, Kian Abdul-Baki2, Andres Urias Rivera3
1Department of Gastroenterology, Hepatology, and Nutrition, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Gastrointestinal infections before immune checkpoint inhibitor (ICI) therapy increase the incidence of immune-mediated colitis (IMC). Prior GI infections also independently raise mortality risk in patients receiving ICIs.
Area of Science:
- Oncology
- Immunology
- Gastroenterology
Background:
- Gastrointestinal (GI) infections and associated dysbiosis can impact immune checkpoint inhibitor (ICI) efficacy.
- These infections may increase the risk of adverse events like colitis during ICI therapy.
- The influence of pre-ICI GI infections on immune-mediated colitis (IMC) and survival requires investigation.
Purpose of the Study:
- To explore the impact of GI infections preceding ICI therapy on the incidence and severity of IMC.
- To assess the effect of prior GI infections on patient survival during ICI treatment.
Main Methods:
- Retrospective review of patients receiving ICIs from January 2010 to February 2024 who developed IMC.
- Screening for IMC and prior GI infections using clinical symptoms and stool tests.
- Collection of demographic, IMC, and GI infection-related clinical data.
Main Results:
- 3.0% of patients (34/1132) had GI infections before ICI therapy, most commonly Clostridioides difficile.
- The incidence of IMC was significantly higher in patients with prior GI infections (8.7%) compared to those without (5.1%).
- Prior GI infection was independently associated with a 1.6-fold increased risk of mortality in patients receiving ICIs.
Conclusions:
- This study is the first to link pre-ICI GI infection to IMC incidence and survival outcomes.
- Prior GI infection increases the incidence of IMC in patients undergoing ICI therapy.
- Pre-existing GI infections are associated with a higher risk of mortality for patients receiving ICIs.
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