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First-line concomitant EGFR-TKI + chemotherapy versus EGFR-TKI alone for advanced EGFR -mutated NSCLC: a meta-analysis of randomized phase III trials.

Authors :
Landre T
Assié JB
Chouahnia K
Des Guetz G
Auliac JB
Chouaïd C
Source :
Expert review of anticancer therapy [Expert Rev Anticancer Ther] 2024 Aug; Vol. 24 (8), pp. 775-780. Date of Electronic Publication: 2024 Jun 03.
Publication Year :
2024

Abstract

Introduction: A tyrosine-kinase inhibitor (TKI) is indicated as a first-line treatment for patients with non-small-cell lung cancer (NSCLC) harboring an epidermal growth-factor - receptor ( EGFR ) mutation. Chemotherapy (ChT) given in combination with an EGFR-TKI in this setting is of interest.<br />Methods: We conducted a meta-analysis of phase III randomized trials comparing EGFR-TKI + ChT vs. EGFR-TKI alone as first-line therapy for advanced NSCLC harboring an activating EGFR mutation.<br />Results: Three studies evaluated gefitinib + ChT (NEJ009, GAP-Brain, and Noronha et al.) and another evaluated osimertinib + ChT (FLAURA-2). Those four eligible studies included 1413 patients with non-squamous NSCLCs, 826 (58%) with an exon-19 deletion (ex19del) and 541 (38%) with EGFR <superscript> L858R </superscript> . The EGFR-TKI + ChT combination was significantly associated with prolonged PFS (hazard ratio [HR]: 0.52 [95% confidence interval (CI): 0.45-0.59]; p  < 0.0001) and OS (HR: 0.69 [0.52-0.93]; p  = 0.01). PFS was particularly improved for patients with brain metastases (HR: 0.41[0.33-0.51]; p  < 0.00001).<br />Conclusions: For patients with untreated, advanced, EGFR -mutated NSCLCs, the EGFR-TKI + ChT combination, compared to EGFR-TKI alone, was associated with significantly prolonged PFS and OS. However, further studies are needed to identify which patients will benefit the most from the combination.<br />Registration: PROSPERO CRD42024508055.

Details

Language :
English
ISSN :
1744-8328
Volume :
24
Issue :
8
Database :
MEDLINE
Journal :
Expert review of anticancer therapy
Publication Type :
Academic Journal
Accession number :
38813930
Full Text :
https://doi.org/10.1080/14737140.2024.2362889