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
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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.
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