Abstract |
Background: The advent of PD-1/L1 inhibitors has changed the landscape for patients with non-small-cell lung cancer (NSCLC). Meanwhile, the adverse events of PD-1/L1 inhibitors have been focused. Methods: The Cochrane Central Register of Controlled Trials, PubMed and Embase databases and ClinicalTrials.gov were searched from inception to February 2021. Results: 18 studies involving 11,394 patients with NSCLC were included. PD-1/L1 inhibitor monotherapy was associated (relative risk, 95% confidence interval) with an increased risk of pericardial effusion (2.72 [1.45-5.12]; p = 0.002) and cardiac tamponade (2.76 [1.15-6.62]; p = 0.023), whereas PD-1/L1 inhibitors combined with chemotherapy did not increase the risk of pericardial effusion and cardiac tamponade (3.08 [0.93-10.21]; p = 0.066 and 3.27 [0.37-28.94]; p = 0.288, respectively). Conclusion: For patients with NSCLC, treatment with PD-1/L1 inhibitor monotherapy increases the risk of pericardial effusion and cardiac tamponade, but PD-1/L1 inhibitors combined with chemotherapy do not.
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Authors | Honglin Li, Deting Han, Lei Zhang, Xiaoteng Feng, Huijie Li, Feiran Yang, Lucheng Song, Xiurong Li |
Journal | Immunotherapy
(Immunotherapy)
Vol. 14
Issue 7
Pg. 577-592
(05 2022)
ISSN: 1750-7448 [Electronic] England |
PMID | 35373580
(Publication Type: Journal Article, Meta-Analysis, Review, Research Support, Non-U.S. Gov't, Systematic Review)
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Chemical References |
- B7-H1 Antigen
- Immune Checkpoint Inhibitors
- Programmed Cell Death 1 Receptor
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Topics |
- B7-H1 Antigen
- Carcinoma, Non-Small-Cell Lung
(drug therapy)
- Cardiac Tamponade
(drug therapy, epidemiology)
- Humans
- Immune Checkpoint Inhibitors
(adverse effects)
- Lung Neoplasms
(drug therapy)
- Pericardial Effusion
(drug therapy, epidemiology)
- Programmed Cell Death 1 Receptor
(therapeutic use)
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