Bortolot Martina, Torresan Sara, De Carlo Elisa, Bertoli Elisa, Stanzione Brigida, Del Conte Alessandro, Spina Michele, Bearz Alessandra
Department of Medical Oncology, Centro di Riferimento Oncologico di Aviano (CRO), IRCCS, 33081 Aviano, Italy.
Department of Medicine (DME), University of Udine, 33100 Udine, Italy.
Int J Mol Sci. 2024 Dec 3;25(23):12972. doi: 10.3390/ijms252312972.
Although rare in non-small cell lung cancer (NSCLC), BRAF mutations present considerable therapeutic challenges. While the use of BRAF and MEK inhibitor combinations has significantly improved survival outcomes in patients with BRAF V600E mutations, no targeted therapies are currently available for class II and III mutations, leaving the optimal treatment strategy and prognosis for these patients uncertain. Additionally, despite immunotherapy typically showing limited benefit in patients with other activating genomic alterations, it appears to deliver comparable efficacy in BRAF-mutated NSCLC, emerging as a potentially viable treatment option, particularly in patients with a history of smoking. However, resistance to BRAF pathway inhibitors is inevitable, leading to disease progression, and a well-defined strategy to overcome these resistance mechanisms is lacking. This review aims to explore the critical challenges in the management of BRAF-mutated NSCLC, providing a comprehensive summary of the current evidence and highlighting ongoing clinical trials that aim to address these critical gaps.
虽然BRAF突变在非小细胞肺癌(NSCLC)中很少见,但却带来了相当大的治疗挑战。虽然使用BRAF和MEK抑制剂联合疗法已显著改善了BRAF V600E突变患者的生存结果,但目前尚无针对II类和III类突变的靶向治疗方法,这些患者的最佳治疗策略和预后尚不确定。此外,尽管免疫疗法在其他具有激活基因组改变的患者中通常显示出有限的益处,但在BRAF突变的NSCLC中似乎具有相当的疗效,成为一种潜在可行的治疗选择,特别是在有吸烟史的患者中。然而,对BRAF通路抑制剂的耐药性是不可避免的,会导致疾病进展,并且缺乏克服这些耐药机制的明确策略。本综述旨在探讨BRAF突变NSCLC治疗中的关键挑战,全面总结当前证据,并突出旨在填补这些关键空白的正在进行的临床试验。