Department of Pathology, and.
Cancer Research Division, Peter MacCallum Cancer Centre, Melbourne, Australia.
J Clin Invest. 2019 May 1;129(5):1940-1945. doi: 10.1172/JCI123089. Epub 2019 Mar 5.
BRAF and CRAF are critical components of the MAPK signaling pathway which is activated in many cancer types. In approximately 1% of melanomas, BRAF or CRAF are activated through structural arrangements. We describe here a metastatic melanoma with a GOLGA4-RAF1 fusion and pathogenic variants in CTNNB1 and CDKN2A. Anti-CTLA4/anti-PD1 combination immunotherapy failed to control tumor progression. In the absence of other actionable variants the patient was administered MEK inhibitor therapy on the basis of its potential action against RAF1 fusions. This resulted in a profound and clinically significant response. We demonstrated that GOLGA4-RAF1 expression was associated with ERK activation, elevated expression of the RAS/RAF downstream co-effector ETV5, and a high Ki67 index. These findings provide a rationale for the dramatic response to targeted therapy. This study shows that thorough molecular characterization of treatment-resistant cancers can identify therapeutic targets and personalize management, leading to improved patient outcomes.
BRAF 和 CRAF 是 MAPK 信号通路的关键组成部分,该通路在许多癌症类型中被激活。在大约 1%的黑色素瘤中,BRAF 或 CRAF 通过结构排列被激活。我们在这里描述了一例转移性黑色素瘤,其存在 GOLGA4-RAF1 融合以及 CTNNB1 和 CDKN2A 的致病性变异。抗 CTLA4/抗 PD1 联合免疫疗法未能控制肿瘤进展。在没有其他可操作变异的情况下,根据 RAF1 融合可能的作用,给患者施用 MEK 抑制剂治疗。这导致了深刻和具有临床意义的反应。我们证明 GOLGA4-RAF1 的表达与 ERK 激活、RAS/RAF 下游共效应物 ETV5 的高表达以及高 Ki67 指数有关。这些发现为靶向治疗的显著反应提供了依据。本研究表明,对耐药性癌症进行彻底的分子特征分析可以确定治疗靶点并实现个体化管理,从而改善患者的预后。