Risk of interstitial lung disease with the use of programmed cell death 1 (PD-1) inhibitor compared with programmed cell death ligand 1 (PD-L1) inhibitor in patients with breast cancer: A systematic review and meta-analysis

Programmed cell death 1 (PD-1) and programmed cell death ligand 1 (PD-L1) inhibitors have become integral elements within the current landscape of breast cancer treatment modalities; however, they are associated with interstitial lung disease (ILD), which is rare but potentially fatal. Notably, only...

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Veröffentlicht in:Cancer pathogenesis and therapy 2024-04, Vol.2 (2), p.91-102
Hauptverfasser: Guo, Lijuan, Lin, Xiaoyi, Lin, Xin, Wang, Yulei, Lin, Jiali, Zhang, Yi, Chen, Xiangqing, Chen, Miao, Zhang, Guochun, Zhang, Yifang
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Sprache:eng
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Zusammenfassung:Programmed cell death 1 (PD-1) and programmed cell death ligand 1 (PD-L1) inhibitors have become integral elements within the current landscape of breast cancer treatment modalities; however, they are associated with interstitial lung disease (ILD), which is rare but potentially fatal. Notably, only a few studies have compared the difference in ILD incidence between PD-1 and PD-L1 inhibitors. Therefore, this study aimed to assess the discrepancies regarding ILD risk between the two immune checkpoint inhibitors. We also reported three cases of ILD after PD-1 inhibitor treatment. We comprehensively searched PubMed, EMBASE, and the Cochrane Library to identify clinical trials that investigated PD-1/PD-L1 inhibitor treatment for patients with breast cancer. Pooled overall estimates of incidence and risk ratio (RR) were calculated with a 95% confidence interval (CI), and a mirror group analysis was performed using eligible studies. This meta-analysis included 29 studies with 4639 patients who received PD-1/PD-L1 inhibitor treatment. A higher ILD incidence was observed among 2508 patients treated with PD-1 inhibitors than among 2131 patients treated with PD-L1 inhibitors (0.05 vs. 0.02). The mirror group analysis further revealed a higher ILD event risk in patients treated with PD-1 inhibitors than in those treated with PD-L1 inhibitors (RR = 2.34, 95% CI, 1.13–4.82, P = 0.02). Our findings suggest a greater risk of ILD with PD-1 inhibitors than with PD-L1 inhibitors. These findings are instrumental for clinicians in treatment deliberations, and the adoption of more structured diagnostic approaches and management protocols is necessary to mitigate the risk of ILD. [Display omitted] •Programmed cell death 1 (PD-1) and programmed cell death ligand 1 (PD-L1) inhibitors cause interstitial lung disease (ILD).•ILD is a rare adverse event; most cases are low-grade but potentially fatal.•The present meta-analysis included 29 studies with 4639 patients with breast cancer.•Compared with PD-L1 inhibitors, PD-1 inhibitors will increase the risk of ILD in patients with breast cancer.•Suitable treatment options for ILD and its early detection and immediate management should be initiated.
ISSN:2949-7132
2097-2563
2949-7132
DOI:10.1016/j.cpt.2023.08.002