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Multicenter Observational Study on Metastatic Non-Small Cell Lung Cancer Harboring BRAF Mutations: Focus on Clinical Characteristics and Treatment Outcome of V600E and Non-V600E Subgroups.

Authors :
Perrone F
Mazzaschi G
Minari R
Verzè M
Azzoni C
Bottarelli L
Nizzoli R
Pluchino M
Altimari A
Gruppioni E
Sperandi F
Andrini E
Guaitoli G
Bertolini F
Barbieri F
Bettelli S
Longo L
Pagano M
Bonelli C
Tagliavini E
Nicoli D
Ubiali A
Zangrandi A
Trubini S
Proietto M
Gnetti L
Tiseo M
Source :
Cancers [Cancers (Basel)] 2022 Apr 16; Vol. 14 (8). Date of Electronic Publication: 2022 Apr 16.
Publication Year :
2022

Abstract

Introduction: BRAF mutation involved 2-4% of lung adenocarcinoma. Differences in clinicopathologic features and patient outcome exist between V600E and non-V600E BRAF mutated NSCLC. Thus, we sought to assess the frequency and clinical relevance of BRAF mutations in a real-life population of advanced-NSCLC, investigating the potential prognostic significance of distinct genetic alterations.<br />Materials and Methods: The present multicenter Italian retrospective study involved advanced BRAF mutant NSCLC. Complete clinicopathologic data were evaluated for BRAF V600E and non-V600E patients.<br />Results: A total of 44 BRAF <superscript>mut</superscript> NSCLC patients were included (V600E, n = 23; non-V600E, n = 21). No significant differences in survival outcome and treatment response were documented, according to V600E vs. non-V600E mutations, although a trend towards prolonged PFS was observed in the V600E subgroup (median PFS = 11.3 vs. 6.0 months in non-V600E). In the overall population, ECOG PS and age significantly impacted on OS, while bone lesions were associated with shorter PFS. Compared to immunotherapy, first-line chemotherapy was associated with longer OS in the overall population, and especially in the BRAF V600E subtype.<br />Conclusions: Here, we report on real-life data from a retrospective cohort of advanced-NSCLC harboring BRAF alterations. Our study offers relevant clues on survival outcome, therapeutic response, and clinicopathologic correlations of BRAF-mutant NSCLC.

Details

Language :
English
ISSN :
2072-6694
Volume :
14
Issue :
8
Database :
MEDLINE
Journal :
Cancers
Publication Type :
Academic Journal
Accession number :
35454926
Full Text :
https://doi.org/10.3390/cancers14082019