Perrone Fabiana, Mazzaschi Giulia, Minari Roberta, Verzè Michela, Azzoni Cinzia, Bottarelli Lorena, Nizzoli Rita, Pluchino Monica, Altimari Annalisa, Gruppioni Elisa, Sperandi Francesca, Andrini Elisa, Guaitoli Giorgia, Bertolini Federica, Barbieri Fausto, Bettelli Stefania, Longo Lucia, Pagano Maria, Bonelli Candida, Tagliavini Elena, Nicoli Davide, Ubiali Alessandro, Zangrandi Adriano, Trubini Serena, Proietto Manuela, Gnetti Letizia, Tiseo Marcello
Medical Oncology Unit, University Hospital of Parma, 43126 Parma, Italy.
Department of Medicine and Surgery, University of Parma, 43126 Parma, Italy.
Cancers (Basel). 2022 Apr 16;14(8):2019. doi: 10.3390/cancers14082019.
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.
The present multicenter Italian retrospective study involved advanced BRAF mutant NSCLC. Complete clinicopathologic data were evaluated for BRAF V600E and non-V600E patients.
A total of 44 BRAF NSCLC patients were included (V600E, = 23; non-V600E, = 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.
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.
BRAF突变在2%-4%的肺腺癌中存在。V600E和非V600E BRAF突变的非小细胞肺癌(NSCLC)在临床病理特征和患者预后方面存在差异。因此,我们试图评估晚期NSCLC真实人群中BRAF突变的频率和临床相关性,研究不同基因改变的潜在预后意义。
本项意大利多中心回顾性研究纳入了晚期BRAF突变NSCLC患者。对BRAF V600E和非V600E患者的完整临床病理数据进行评估。
共纳入44例BRAF NSCLC患者(V600E组23例;非V600E组21例)。根据V600E与非V600E突变情况,生存结局和治疗反应未发现显著差异,尽管在V600E亚组中观察到无进展生存期(PFS)有延长趋势(V600E组中位PFS = 11.3个月,非V600E组为6.0个月)。在总体人群中,东部肿瘤协作组(ECOG)体能状态评分和年龄对总生存期(OS)有显著影响,而骨转移与较短的PFS相关。与免疫治疗相比,一线化疗在总体人群中,尤其是在BRAF V600E亚型中与更长的OS相关。
在此,我们报告了一组晚期NSCLC BRAF改变患者回顾性队列的真实数据。我们的研究为BRAF突变NSCLC的生存结局、治疗反应及临床病理相关性提供了相关线索。