TY - JOUR
T1 - Overall survival benefits of first-line EGFR tyrosine kinase inhibitors in EGFR-mutated non-small-cell lung cancers
T2 - A systematic review and meta-analysis
AU - Kuan, Feng Che
AU - Kuo, Liang Tseng
AU - Chen, Min Chi
AU - Yang, Cheng Ta
AU - Shi, Chung Sheng
AU - Teng, David
AU - Lee, Kuan Der
N1 - Funding Information:
Data source and search strategy. A comprehensive search to identify all published RCTs that compared the outcomes of TKI vs chemotherapy for NSCLC was done. MEDLINE, EMBASE, and the Cochrane Central Register of Controlled Trials (CENTRAL) were searched for relevant trials from inception to 31 January 2015. The search strategy was a combination of the terms ‘EGFR’, ‘epidermal growth factor receptor’, ‘tyrosine kinase inhibitors’, ‘TKI’, ‘exon’, ‘mutation’, ‘non-small-cell lung cancer’, and ‘NSCLC’ without restrictions on language and gender. Additional searches through Google Scholar and the United States National Institutes of Health trials register (http://clinicaltrial.gov), and a manual search through reference lists of pertinent reviews and studies were performed. Two authors conducted the search independently with no language or date restrictions set. Lastly, a pharmaceutical company (F. Hoffmann-La Roche Ltd) was contacted for information on unpublished trials.
Publisher Copyright:
© 2015 Cancer Research UK. All rights reserved.
PY - 2015/11/17
Y1 - 2015/11/17
N2 - Background:Accumulating data shows that exon 19 deletions and L858R, both activating epidermal growth factor receptor mutations in non-small-cell lung cancers (NSCLCs), are just two different entities in terms of prognosis and treatment response to tyrosine kinase inhibitors (TKIs).Methods:A systematic review and meta-analysis of randomized controlled trials comparing TKIs with conventional chemotherapy was performed. Eight trials of 1498 patients and five trials of 1279 patients with either exon 19 deletions or L858R were included in the meta-analysis.Results:TKI treatment demonstrated progression-free survival benefit in patients with exon 19 deletions (hazard ratio (HR): 0.27, 95% confidence interval (CI): 0.21-0.35) and L858R (HR: 0.45, 95% CI: 0.35-0.58). Patients with exon 19 deletions had significant overall survival (OS) benefit under TKI treatment (HR: 0.72, 95% CI: 0.60-0.88). Subgroup analyses showed that irreversible TKIs, but not reversible TKIs, had statistically significant OS benefit in these patients (irreversible TKIs, HR: 0.59, 95% CI: 0.47-0.73; reversible TKIs, HR: 0.84, 95% CI: 0.69-1.02). Patients with L858R demonstrated no OS benefit under first-line TKI use (HR: 1.15, 95% CI: 0.95-1.39).Conclusions:In patients with advanced NSCLC harbouring exon 19 deletions, TKIs are associated with better OS compared with conventional chemotherapy. Future clinical trials should take exon 19 deletions and L858R as distinct disease entities and evaluate the treatment efficacy separately.
AB - Background:Accumulating data shows that exon 19 deletions and L858R, both activating epidermal growth factor receptor mutations in non-small-cell lung cancers (NSCLCs), are just two different entities in terms of prognosis and treatment response to tyrosine kinase inhibitors (TKIs).Methods:A systematic review and meta-analysis of randomized controlled trials comparing TKIs with conventional chemotherapy was performed. Eight trials of 1498 patients and five trials of 1279 patients with either exon 19 deletions or L858R were included in the meta-analysis.Results:TKI treatment demonstrated progression-free survival benefit in patients with exon 19 deletions (hazard ratio (HR): 0.27, 95% confidence interval (CI): 0.21-0.35) and L858R (HR: 0.45, 95% CI: 0.35-0.58). Patients with exon 19 deletions had significant overall survival (OS) benefit under TKI treatment (HR: 0.72, 95% CI: 0.60-0.88). Subgroup analyses showed that irreversible TKIs, but not reversible TKIs, had statistically significant OS benefit in these patients (irreversible TKIs, HR: 0.59, 95% CI: 0.47-0.73; reversible TKIs, HR: 0.84, 95% CI: 0.69-1.02). Patients with L858R demonstrated no OS benefit under first-line TKI use (HR: 1.15, 95% CI: 0.95-1.39).Conclusions:In patients with advanced NSCLC harbouring exon 19 deletions, TKIs are associated with better OS compared with conventional chemotherapy. Future clinical trials should take exon 19 deletions and L858R as distinct disease entities and evaluate the treatment efficacy separately.
KW - first-line EGFR
KW - NSCLC
KW - overall survival
KW - TKI
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U2 - 10.1038/bjc.2015.356
DO - 10.1038/bjc.2015.356
M3 - Article
C2 - 26461059
AN - SCOPUS:84947487341
SN - 0007-0920
VL - 113
SP - 1519
EP - 1528
JO - British Journal of Cancer
JF - British Journal of Cancer
IS - 10
ER -