Abstract

Background: Recently, immune checkpoint inhibitors (ICIs) have been proved one of the most promising anti-cancer therapy, series clinical trials have confirmed their efficacy. But they are also associated with distinctive set of toxic effects, which are recognized as immune-related adverse events. Among those immune-related adverse events, pneumonitis is rare, but it is often clinically serious and potentially life-threatening. Although many clinical trial results of PD-1/PD-L1 inhibitors had been reported incidence of pneumonitis, the knowledge based on the individual cohort data from each clinical trial is limited. So we conducted a meta-analysis of trials of PD-1/PD-L1 inhibitors in patients with advanced cancer and compared relative risk and incidence among different tumor types and therapeutic regimens. Such an analysis may provide important knowledge of this rare but clinically significant and potentially serious immune-related adverse event.Methods: Electronic databases were used to search eligible literatures, include randomized controlled trials (RCTs) comparing immune checkpoint inhibitors vs. standard therapies. All-grade (1–4) or high-grade (3–4) pneumonitis events were extracted. The summary relative risk, summary incidence, and 95% confidence intervals were calculated.Results: The incidence of all-grade and high-grade pneumonitis in non-small cell lung cancer (NSCLC) was significantly higher compared with other tumor types, such as Melanoma, urothelial carcinoma (UC), head and neck squamous cell carcinoma (HNSCC) (3.1% vs. 2.0%; p = 0.02, 1.4% vs. 0.6%; p = 0.03). The risk of all-grade pneumonitis was obtained from all patients in both experimental arm and control arm. Treatment with immune checkpoint inhibitors targeting PD-1/PD-L1 did significantly increase the risk of all-grade and high-grade pneumonitis compared with controls (fixed effects, RR: 4.70; 95% CI: 2.81–7.85; p < 0.00001, RR: 3.33; 95% CI: 1.68–6.59; p = 0.0006).Conclusion: The incidence of immune checkpoint inhibitors related pneumonitis was higher in NSCLC than other tumor types. Patients treated with immune checkpoint inhibitor in experiment arms are more likely to experience any grade pneumonitis than control arms. These findings suggest that clinician need to draw more attention on this rare but serious adverse event.

Highlights

  • In recent years, immunotherapy has become the fourth treatment mode of antitumor treatment

  • To compare the incidence of pneumonitis between non-small-cell lung cancer (NSCLC) and other tumor types, we include tumor types alone as the predictor in the univariate generalized estimating equation models, the incidence of all-grade pneumonitis in NSCLC was significantly higher compared with other tumor types that include Melanoma, urothelial carcinoma (UC), and head and neck squamous cell carcinoma (HNSCC) (3.1% vs. 2.0%; p = 0.02) (Figures 3, 5), and the incidence of high grade pneumonitis in NSCLC was higher compare with other tumor types (1.4% vs. 0.6%; p = 0.03) (Figures 6, 7)

  • We evaluated the risk of pneumonitis related to different type of immune checkpoint inhibitors (ICIs) (Figures 10, 11)

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Summary

Introduction

Immunotherapy has become the fourth treatment mode of antitumor treatment. The remarkable efficacy of ICIs has been shown, they are associated with distinctive set of toxic effects, which are recognized as immune-related adverse event, such as pruritus, rash, diarrhea, colitis, hypophysitis, thyroiditis, pancreatitis, nephritis, elevated liver function tests, and pneumonitis (Fujii et al, 2017; Kumar et al, 2017; Nagai and Muto, 2018). Immune checkpoint inhibitors (ICIs) have been proved one of the most promising anti-cancer therapy, series clinical trials have confirmed their efficacy They are associated with distinctive set of toxic effects, which are recognized as immune-related adverse events. We conducted a meta-analysis of trials of PD-1/PD-L1 inhibitors in patients with advanced cancer and compared relative risk and incidence among different tumor types and therapeutic regimens Such an analysis may provide important knowledge of this rare but clinically significant and potentially serious immune-related adverse event

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