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Meta-Analysis
. 2021 Apr;12(7):1084-1095.
doi: 10.1111/1759-7714.13874. Epub 2021 Mar 4.

The role of EGFR-TKIs as adjuvant therapy in EGFR mutation-positive early-stage NSCLC: A meta-analysis

Affiliations
Meta-Analysis

The role of EGFR-TKIs as adjuvant therapy in EGFR mutation-positive early-stage NSCLC: A meta-analysis

Chutong Lin et al. Thorac Cancer. 2021 Apr.

Abstract

Background: The role of adjuvant epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) is not clear in early-stage nonsmall-cell lung cancer (NSCLC) patients. This meta-analysis aims to compare the efficacy and safety of EGFR-TKIs as adjuvant therapy with chemotherapy or placebo in NSCLC patients harboring EGFR mutations.

Patients and methods: Pubmed, Embase, and Cochrane databases were searched for randomized controlled trials. The hazard ratio (HR) of disease-free survival (DFS) and overall survival (OS) as well as the risk ratio (RR) of severe adverse events were merged.

Results: Seven articles from five studies from 1843 records, a total of 1227 patients, were included in the analysis. The HR for DFS was 0.38 (95% confidence interval [CI] 0.22-0.63), in favor of EGFR-TKIs. However, no significant benefit of OS was seen (HR = 0.61, 95% CI 0.31-1.22). Treatment benefit was more pronounced in patients with advanced disease stage and longer duration of medication, EGFR exon 19 deletion mutation, and treatment with third-generation EGFR-TKIs. Adjuvant targeted therapy may cause few adverse events compared with chemotherapy (RR = 0.28, 95% CI 0.09-0.94). The possibility of severe adverse events for the first-generation drugs was significantly lower than for third-generation drugs.

Conclusion: In EGFR mutation-positive patients with stage IB-IIIA NSCLC, compared with adjuvant chemotherapy or placebo, adjuvant EGFR-TKIs should effectively improve the patient's DFS, but not effectively improve OS. Disease stage, treatment duration, mutation types, and therapeutic drugs could affect the degree of benefit. Adjuvant EGFR-TKIs had more favorable tolerability than chemotherapy, especially with the usage of first-generation drugs.

Keywords: adjuvant treatment; epidermal growth factor receptor tyrosine kinase inhibitors; nonsmall-cell lung cancer; survival; targeted therapy.

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Figures

FIGURE 1
FIGURE 1
Flow chart of selection strategy
FIGURE 2
FIGURE 2
Assessment of study quality included in the meta‐analysis by Cochrane collaboration's tool for assessing risk of bias.Note: Low and high scores given for the seven parameters assessed represented by ‘+’ and ‘−’
FIGURE 3
FIGURE 3
Forest plot for hazard ratio on DFS and OS. (a) Forest plot of hazard ratio of DFS. (b) Sensitivity analysis for DFS. (c) Forest plot of hazard ratio of OS. (d) Sensitivity analysis for OS
FIGURE 4
FIGURE 4
Subgroup analysis for OS for patients receiving adjuvant EGFR‐TKIs. (a) Forest plot of hazard ratio of OS for adjuvant EGFR TKI according to disease stages. (b) Forest plot of hazard ratio of OS for adjuvant EGFR TKI according to median treatment duration
FIGURE 5
FIGURE 5
Forest plots of relative risk of severe adverse events. (a) Forest plot of risk ratio of severe adverse events associated with adjuvant EGFR‐TKIs versus chemotherapy. (b) Forest plot of risk ratio of severe adverse events associated with adjuvant EGFR‐TKIs versus placebo. (c) Subgroup analysis of risk ratio of severe adverse events for adjuvant EGFR‐TKIs versus placebo according to EGFR TKI type
FIGURE 6
FIGURE 6
Forest plot for adverse events analysis excluding the study of Li et al. (a) Forest plot of risk ratio of severe adverse events for adjuvant EGFR‐TKIs versus placebo without the study of Li et al. (b) Forest plot on subgroup analysis of risk ratio of severe adverse events for adjuvant EGFR‐TKIs versus placebo according to different kind of drugs without the study of Li et al.

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