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Article

The Risk of Diarrhea and Colitis in Patients with Lung Cancer Treated with Immune Checkpoint Inhibitors: A Systematic Review and Meta-Analysis

by
K. Bishay
1,*,
P. Tandon
1,
S. Bourassa-Blanchette
2,
S.A. Laurie
3 and
J.D. McCurdy
4,5
1
Division of Gastroenterology, University of Toronto, Toronto, ON, Canada
2
Division of Infectious Diseases, University of Calgary, Calgary, AB, Canada
3
Division of Medical Oncology, The Ottawa Hospital, Ottawa, ON, Canada
4
Division of Gastroenterology, The Ottawa Hospital, Ottawa, ON, Canada
5
The Ottawa Hospital Research Institute, The Ottawa Hospital, Ottawa, ON, Canada
*
Author to whom correspondence should be addressed.
Curr. Oncol. 2020, 27(5), 486-494; https://0-doi-org.brum.beds.ac.uk/10.3747/co.27.6251
Submission received: 2 July 2020 / Revised: 11 August 2020 / Accepted: 11 September 2020 / Published: 1 October 2020

Abstract

Background: Immune checkpoint inhibitors (icis), including inhibitors of PD-1, PD-L1, and ctla-4, are relatively novel therapies for lung cancer, although their use might be limited by gastrointestinal toxicity. The aim of the present study was to determine the risk of diarrhea and colitis associated with icis in lung cancer and the rates of discontinuation because of those toxicities. Methods: Electronic databases were searched for prospective trials reporting the risk of diarrhea and colitis in patients with lung cancer treated with PD-1, PD-L1, and ctla-4 inhibitors. The incidences of diarrhea and colitis and their grades were assessed clinically using standardized reporting criteria. Pooled incidence and weighted relative risk estimates for diarrhea and colitis with 95% confidence intervals (cis) were estimated using a random effects model. The incidence of discontinuations for gi toxicity was also calculated. Results: Twenty-seven studies were included: sixteen studies with PD-1 inhibitors, nine studies with PD-L1 inhibitors, and four studies combining PD-based strategies with ctla-4 inhibitors. The incidence of all-grade diarrhea was 9.1% (95% ci: 7.8% to 10.5%) for anti–PD-1 therapy and 11.0% (95% ci: 7.5% to 14.5%) for anti–PD-L1 therapy. The incidence of all-grade colitis was 0.9% (95% ci: 0.4% to 1.3%) for anti–PD-1 therapy and 0.4% (95% ci: 0.0% to 0.8%) for anti–PD-L1 therapy. The relative risk for all-grade diarrhea was higher with combination anti–PD-1 and anti–ctla-4 than with anti–PD-1 monotherapy (relative risk: 1.61; 95% ci: 1.14 to 2.29). Anti–PD-1 therapy was discontinued in 4.1% of patients with diarrhea (95% ci: 0.7% to 7.4%) and in 35.7% of those with colitis (95% ci: 0.0% to 81.1%); combination therapy was discontinued in 10.1% of patients with diarrhea (95% ci: 4.8% to 15.4%) and in 39.9% of those with colitis (95% ci: 3.9% to 75.9%). Conclusions: Diarrhea is a relatively frequently encountered gi toxicity when ici therapy is used in lung cancer treatment. Colitis is less frequently encountered, although when it does occur, it often results in therapy discontinuation.
Keywords: lung cancer; checkpoint inhibitors; immunotherapy; diarrhea; colitis lung cancer; checkpoint inhibitors; immunotherapy; diarrhea; colitis

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MDPI and ACS Style

Bishay, K.; Tandon, P.; Bourassa-Blanchette, S.; Laurie, S.A.; McCurdy, J.D. The Risk of Diarrhea and Colitis in Patients with Lung Cancer Treated with Immune Checkpoint Inhibitors: A Systematic Review and Meta-Analysis. Curr. Oncol. 2020, 27, 486-494. https://0-doi-org.brum.beds.ac.uk/10.3747/co.27.6251

AMA Style

Bishay K, Tandon P, Bourassa-Blanchette S, Laurie SA, McCurdy JD. The Risk of Diarrhea and Colitis in Patients with Lung Cancer Treated with Immune Checkpoint Inhibitors: A Systematic Review and Meta-Analysis. Current Oncology. 2020; 27(5):486-494. https://0-doi-org.brum.beds.ac.uk/10.3747/co.27.6251

Chicago/Turabian Style

Bishay, K., P. Tandon, S. Bourassa-Blanchette, S.A. Laurie, and J.D. McCurdy. 2020. "The Risk of Diarrhea and Colitis in Patients with Lung Cancer Treated with Immune Checkpoint Inhibitors: A Systematic Review and Meta-Analysis" Current Oncology 27, no. 5: 486-494. https://0-doi-org.brum.beds.ac.uk/10.3747/co.27.6251

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