Treatment-Related Adverse Events of Combination EGFR Tyrosine Kinase Inhibitor and Immune Checkpoint Inhibitor in EGFR-Mutant Advanced Non-Small Cell Lung Cancer: A Systematic Review and Meta-Analysis

(1) Background: We performed a meta-analysis to examine whether combined epidermal growth factor tyrosine kinase inhibitor (EGFR-TKI) and immune checkpoint inhibitor (ICI) increases treatment-related adverse events (trAEs) in advanced non-small cell lung cancer (NSCLC). (2) Methods: Articles from ME...

Full description

Saved in:
Bibliographic Details
Published inCancers Vol. 14; no. 9; p. 2157
Main Authors Chan, Daisy Wai-Ka, Choi, Horace Cheuk-Wai, Lee, Victor Ho-Fun
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 26.04.2022
MDPI
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:(1) Background: We performed a meta-analysis to examine whether combined epidermal growth factor tyrosine kinase inhibitor (EGFR-TKI) and immune checkpoint inhibitor (ICI) increases treatment-related adverse events (trAEs) in advanced non-small cell lung cancer (NSCLC). (2) Methods: Articles from MEDLINE, EMBASE, and Cochrane databases were searched. Proportions and odds ratios (ORs) of the pooled incidence of overall and organ-specific trAEs in combination EGFR-TKI and ICI were compared to TKI monotherapy. (3) Results: Eight studies fulfilled our selection criteria. Any-grade organ-specific trAEs were more common in combination EGFR-TKI and ICI than TKI monotherapy (skin: OR = 1.19, = 0.012; gastrointestinal tract: OR = 1.04, = 0.790; ILD: OR = 1.28, = 0.001). Grade ≥ 3 trAEs were also more frequent in combination treatment (skin: OR = 1.13, = 0.082; gastrointestinal tract: OR = 1.13, = 0.076; ILD: OR = 1.16, = 0.003). (4) Conclusions: A higher proportion of grade ≥3 skin and gastrointestinal trAEs and ILDs was observed in combination TKI and ICI compared to TKI alone. Caution has to be taken when interpreting the results owing to the small number of studies included in this meta-analysis.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
ObjectType-Review-3
content type line 23
ISSN:2072-6694
2072-6694
DOI:10.3390/cancers14092157