Back to Search Start Over

Differences in the risk of immune-related pneumonitis between PD-1 and PD-L1 inhibitors: a meta-analysis according to the new mirror-principle and PRISMA guidelines.

Authors :
Tian, Yuan
Yin, Zongxiu
Zhang, Chi
Li, Zhuoqi
Wang, Yuanyuan
Zhang, Kai
Chen, Feng
Dang, Qi
Source :
Cancer Immunology, Immunotherapy; Sep2024, Vol. 73 Issue 9, p1-16, 16p
Publication Year :
2024

Abstract

Purpose: To compare the risk of immune-associated pneumonitis between PD-1 and PD-L1 inhibitors, the meta-analysis was designed. Method: The difference in risk of immune-associated pneumonitis between PD-1 and PD-L1 inhibitors was assessed by two different meta-analysis methods, the Mirror-pairing and the PRISMA guidelines. Results: A total of eighty-eight reports were used for meta-analysis, while thirty-two studies were used for the Mirror-pairing. Both PD-1 and PD-L1 inhibitors (used alone or combined with chemotherapy) increased the risk of developing immune-related pneumonitis (P < 0.00001; P < 0.00001). Based on indirect analyses results (subgroup analyses), the risk of PD-L1-induced pneumonitis was weaker than that of PD-1 inhibitors when the control group was chemotherapy (OR = 3.33 vs. 5.43) or placebo (OR = 2.53 vs. 3.19), while no obvious significant differences were found (P = 0.17; P = 0.53). For the Mirror-pairing-based meta-analysis, the risk of PD-1-induced pneumonitis was significantly higher than that of PD-L1 inhibitors (OR = 1.46, 95%CI [1.08, 1.98], I<superscript>2</superscript> = 0%, Z = 2.47 (P = 0.01)). However, this difference was not significant, when they were combined with chemotherapy (OR = 1.05, 95%CI [0.68, 1.60], I<superscript>2</superscript> = 38%, Z = 0.21 (P = 0.84)). Conclusion: Both PD-1 and PD-L1 inhibitors increased the risk of immune-related pneumonitis, while the risk of PD-1-induced pneumonitis was significantly higher than that of PD-L1 inhibitors. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03407004
Volume :
73
Issue :
9
Database :
Complementary Index
Journal :
Cancer Immunology, Immunotherapy
Publication Type :
Academic Journal
Accession number :
178231339
Full Text :
https://doi.org/10.1007/s00262-024-03736-z