Cancers (Apr 2022)

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

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

DOI
https://doi.org/10.3390/cancers14082019
Journal volume & issue
Vol. 14, no. 8
p. 2019

Abstract

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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.

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