Kudchadkar Ragini, Gibney Geoffrey, Sondak Vernon K
Department of Cutaneous Oncology, Moffitt Cancer Center, Tampa, FL, USA.
Methods Mol Biol. 2014;1102:27-42. doi: 10.1007/978-1-62703-727-3_3.
Personalized melanoma medicine has progressed from histopathologic features to serum markers to molecular profiles. Since the identification of activating BRAF mutations and subsequent development of drugs targeting the mutant BRAF protein, oncologists now need to incorporate prognostic and predictive biomarkers into treatment decisions for their melanoma patients. Examples include subgrouping patients by genotype profiles for targeted therapy and the development of serologic, immunohistochemical, and genotype profiles for the selection of patients for immunotherapies. In this chapter, we provide an overview of the current status of BRAF mutation testing, as well as promising serologic and molecular profiles that will impact patient care. As further research helps clarify the roles of these factors, the clinical outcomes of melanoma patients promise to be greatly improved.
个性化黑色素瘤医学已从组织病理学特征发展到血清标志物,再到分子谱。自从发现激活BRAF突变并随后开发出靶向突变BRAF蛋白的药物以来,肿瘤学家现在需要将预后和预测生物标志物纳入其黑色素瘤患者的治疗决策中。例如,通过基因型谱对患者进行亚组划分以进行靶向治疗,以及开发血清学、免疫组织化学和基因型谱以选择免疫治疗的患者。在本章中,我们概述了BRAF突变检测的现状,以及将影响患者护理的有前景的血清学和分子谱。随着进一步的研究有助于阐明这些因素的作用,黑色素瘤患者的临床结局有望得到极大改善。