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尿路上皮癌的新型分子靶点。

Novel molecular targets for urothelial carcinoma.

作者信息

Faltas Bishoy M, Karir Beerinder S, Tagawa Scott T, Rosenberg Jonathan E

机构信息

Weill Cornell Medical College, Division of Hematology and Medical Oncology, Department of Medicine , New York, NY , USA

出版信息

Expert Opin Ther Targets. 2015 Apr;19(4):515-25. doi: 10.1517/14728222.2014.987662. Epub 2015 Jan 30.

Abstract

INTRODUCTION

Urothelial cancer (UC) remains a significant public health problem, with no new second-line agents FDA-approved in the US. Next-generation sequencing technologies are starting to generate a molecular landscape of UC thus revealing novel molecular targets.

AREAS COVERED

In this review, the authors provide a detailed review of novel molecular targets in UC based on published genomic analyses of urothelial tumors. We provide an overview of each molecular target with a brief discussion of therapeutic strategies and clinical trials targeting each pathway.

EXPERT OPINION

UC continues to be a lethal disease with no FDA-approved effective second-line therapies. Platinum resistance continues to be a daunting clinical problem. Next-generation sequencing methods have led to the elucidation of numerous molecular targets in UC, including PI3K, to the elucidation of numerous molecular targets in UC, including PI3K, ERBB2 and FGFR3, among many others. These molecular perturbations can be exploited therapeutically with targeted therapies in patient populations enriched for these molecular alterations, thus paving the way for precision medicine in UC management.

摘要

引言

尿路上皮癌(UC)仍然是一个重大的公共卫生问题,在美国没有新的二线药物获得FDA批准。新一代测序技术开始描绘UC的分子图谱,从而揭示新的分子靶点。

涵盖领域

在本综述中,作者基于已发表的尿路上皮肿瘤基因组分析,对UC中的新分子靶点进行了详细综述。我们概述了每个分子靶点,并简要讨论了针对每个通路的治疗策略和临床试验。

专家观点

UC仍然是一种致命疾病,没有FDA批准的有效的二线治疗方法。铂类耐药仍然是一个严峻的临床问题。新一代测序方法已导致在UC中阐明了众多分子靶点,包括PI3K、ERBB2和FGFR3等。这些分子扰动可通过针对富集这些分子改变的患者群体进行靶向治疗来加以利用,从而为UC管理中的精准医学铺平道路。

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