Gastrointestinal treatment-related adverse events of combined immune checkpoint inhibitors: a meta-analysis

Author:

Karna Rahul1ORCID,S Deliwala Smit2,Ramgopal Balasubramanian3,Asawa Palash1,Mishra Rahul4,P Mohan Babu5,Jayakrishnan Thejus6,Grover Dheera7,Kalra Tanisha8,Bhalla Jaideep9,Saraswati Ushasi9,K Gangwani Manesh10ORCID,Dhawan Manish11,G Adler Douglas12ORCID

Affiliation:

1. Internal Medicine, Allegheny Health Network, Pittsburgh, PA, USA

2. Division of Digestive Diseases, Emory University School of Medicine, Atlanta, GA, USA

3. Foundation Fellowship Doctor, University Hospital, Southampton NHS Foundation Trust, Southampton, Hampshire, UK

4. Postdoctoral research fellow, Cleveland Clinic, OH, USA

5. Gastroenterology & Hepatology, University of Utah Health School of Medicine, Salt Lake City, UT, USA

6. Hematology & Oncology, Cleveland Clinic, Cleveland, OH, USA

7. Internal Medicine, University of Connecticut, Hartford, CT, USA

8. Internal Medicine, SUNY Downstate Health Science University, NY, USA

9. Internal Medicine, Cleveland Clinic, Cleveland, OH, USA

10. Internal Medicine, University of Toledo Medical Center, Toledo, OH, USA

11. Gastroenterology & Hepatology, Allegheny Health Network, Pittsburgh, PA, USA

12. Center for Advanced Therapeutic Endoscopy, Centura Health, Denver, CO, USA

Abstract

Introduction: Combined immune checkpoint inhibitors can cause gastrointestinal adverse events. Methods: We performed a meta-analysis of pooled colonic, hepatic and pancreatic treatment-related adverse events of combined ICI. Results: 53 trials reporting treatment-related adverse events in 6581 patients. All grade diarrhea was the most common adverse event seen in 25.4% patients, followed by all grade hepatitis in nearly 13% patients and pancreatitis in nearly 7.5% patients. Conclusion: Our study provides pooled data of treatment-related adverse events from different combination immune checkpoint inhibitors use in solid tumors and demonstrates a high incidence of all grades and ≥3 grade gastrointestinal adverse events. Further studies are required to characterize these adverse events and assess their overall impact on treatment course and outcomes.

Publisher

Future Medicine Ltd

Subject

Oncology,Immunology,Immunology and Allergy

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