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

Author:

Perrone FabianaORCID,Mazzaschi Giulia,Minari RobertaORCID,Verzè Michela,Azzoni Cinzia,Bottarelli Lorena,Nizzoli Rita,Pluchino Monica,Altimari Annalisa,Gruppioni ElisaORCID,Sperandi Francesca,Andrini Elisa,Guaitoli Giorgia,Bertolini Federica,Barbieri Fausto,Bettelli Stefania,Longo Lucia,Pagano Maria,Bonelli CandidaORCID,Tagliavini Elena,Nicoli Davide,Ubiali Alessandro,Zangrandi Adriano,Trubini Serena,Proietto Manuela,Gnetti Letizia,Tiseo MarcelloORCID

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. 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. Results: A total of 44 BRAFmut 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. 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.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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