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头颈部癌症的分子特征:离个体化靶向治疗还有多远?

Molecular characterization of head and neck cancer: how close to personalized targeted therapy?

机构信息

Department of OtolaryngologyHead and Neck Surgery, Henry Ford Health System, Detroit, MI 48202, USA.

出版信息

Mol Diagn Ther. 2012 Aug 1;16(4):209-22. doi: 10.2165/11635330-000000000-00000.

Abstract

Molecular targeted therapy in head and neck squamous cell carcinoma (HNSCC) continues to make strides, and holds much promise. Cetuximab remains the sole US FDA-approved molecular targeted therapy available for HNSCC, though several new biologic agents targeting the epidermal growth factor receptor (EGFR) and other pathways are currently in the regulatory approval pipeline. While targeted therapies have the potential to be personalized, their current use in HNSCC is not personalized. This is illustrated for EGFR-targeted drugs, where EGFR as a molecular target has yet to be individualized for HNSCC. Future research needs to identify factors that correlate with response (or lack of one) and the underlying genotype-phenotype relationship that dictates this response. Comprehensive exploration of genetic and epigenetic landscapes in HNSCC is opening new frontiers to further enlighten and mechanistically inform newer as well as existing molecular targets, and to set a course for eventually translating these discoveries into therapies for patients. This opinion offers a snapshot of the evolution of molecular subtyping in HNSCC and its current clinical applicability, as well as new emergent paradigms with implications for controlling this disease in the future.

摘要

头颈部鳞状细胞癌(HNSCC)的分子靶向治疗继续取得进展,前景广阔。西妥昔单抗仍然是唯一获得美国食品和药物管理局(FDA)批准用于 HNSCC 的分子靶向治疗药物,尽管目前有几种针对表皮生长因子受体(EGFR)和其他途径的新型生物制剂正在进行监管审批。尽管靶向治疗有可能实现个性化,但目前在 HNSCC 中的应用并非个性化。这在针对 EGFR 的药物中得到了体现,EGFR 作为一个分子靶点尚未针对 HNSCC 进行个体化。未来的研究需要确定与反应(或缺乏反应)相关的因素,以及决定这种反应的潜在基因型-表型关系。对头颈部鳞状细胞癌的遗传和表观遗传景观进行全面探索,为进一步阐明和从机制上了解新的和现有的分子靶点开辟了新的前沿,并为最终将这些发现转化为患者的治疗方法奠定了基础。本观点概述了 HNSCC 分子亚型的演变及其目前的临床适用性,以及新出现的范式对未来控制这种疾病的影响。

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