Impact of smoking status on the relative efficacy of the EGFR TKI/angiogenesis inhibitor combination therapy in advanced NSCLC-a systematic review and meta-analysis.

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State: Public
Version: Final published version
License: CC BY-NC-ND 4.0
Serval ID
serval:BIB_EABD7EDC5C76
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Impact of smoking status on the relative efficacy of the EGFR TKI/angiogenesis inhibitor combination therapy in advanced NSCLC-a systematic review and meta-analysis.
Journal
ESMO open
Author(s)
Dafni U., Soo R.A., Peters S., Tsourti Z., Zygoura P., Vervita K., Han J.Y., De Castro J., Coate L., Früh M., Hashemi SMS, Nadal E., Carcereny E., Sala M.A., Bernabé R., Provencio M., Cuffe S., Roschitzki-Voser H., Ruepp B., Rosell R., Stahel R.A.
ISSN
2059-7029 (Electronic)
ISSN-L
2059-7029
Publication state
Published
Issued date
06/2022
Peer-reviewed
Oui
Volume
7
Number
3
Pages
100507
Language
english
Notes
Publication types: Journal Article ; Meta-Analysis ; Systematic Review ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Abstract
The ETOP 10-16 BOOSTER trial failed to demonstrate a progression-free survival (PFS) benefit for adding bevacizumab to osimertinib in second line. An exploratory subgroup analysis, however, suggested a PFS benefit of the combination in patients with a smoking history and prompted us to do this study.
A systematic review and meta-analysis to evaluate the differential effect of smoking status on the benefit of adding an angiogenesis inhibitor to epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor therapy was carried out. All relevant randomized controlled trials appearing in main oncology congresses or in PubMed as of 1 November 2021 were used according to the Preferred Reporting Items for Systematic Review and Meta-Analyses statement. Primarily PFS according to smoking status, and secondarily overall survival (OS) were of interest. Pooled and interaction hazard ratios (HRs) were estimated by fixed or random effects models, depending on the detected degree of heterogeneity. Bias was assessed using the revised Cochrane tool for randomized controlled trials (RoB 2).
Information by smoking was available for 1291 patients for PFS (seven studies) and 678 patients for OS (four studies). The risk of bias was low for all studies. Combination treatment significantly prolonged PFS for smokers [n = 502, HR = 0.55, 95% confidence interval (CI): 0.44-0.69] but not for nonsmokers (n = 789, HR = 0.92, 95% CI: 0.66-1.27; treatment-by-smoking interaction P = 0.02). Similarly, a significant OS benefit was found for smokers (n = 271, HR = 0.66, 95% CI: 0.47-0.93) but not for nonsmokers (n = 407, HR = 1.07, 95% CI: 0.82-1.42; treatment-by-smoking interaction P = 0.03).
In advanced EGFR-non-small-cell lung cancer patients, the addition of an angiogenesis inhibitor to EGFR-tyrosine kinase inhibitor therapy provides a statistically significant PFS and OS benefit in smokers, but not in non-smokers. The biological basis for this observation should be pursued and could determine whether this might be due to a specific co-mutational pattern produced by tobacco exposure.
Keywords
Angiogenesis Inhibitors/pharmacology, Angiogenesis Inhibitors/therapeutic use, Antineoplastic Agents/therapeutic use, Carcinoma, Non-Small-Cell Lung/drug therapy, ErbB Receptors, Humans, Lung Neoplasms/drug therapy, Protein Kinase Inhibitors/pharmacology, Protein Kinase Inhibitors/therapeutic use, Smoking/adverse effects, Smoking/epidemiology, EGFR mutations, EGFR-TKI, NSCLC, randomised controlled trial, smoking status
Pubmed
Web of science
Open Access
Yes
Create date
21/06/2022 13:20
Last modification date
25/01/2024 8:46
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