Novel molecular targets for urothelial carcinoma

被引:9
作者
Faltas, Bishoy M. [1 ]
Karir, Beerinder S. [1 ]
Tagawa, Scott T. [1 ]
Rosenberg, Jonathan E. [2 ]
机构
[1] Weill Cornell Med Coll, Div Hematol & Med Oncol, Dept Med, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Weill Cornell Med Coll, Dept Med, New York, NY 10021 USA
关键词
genomics; molecular targets; targeted therapy; urothelial carcinoma; HUMAN BLADDER-CANCER; TRANSITIONAL-CELL CARCINOMA; SUBEROYLANILIDE HYDROXAMIC ACID; HISTONE DEACETYLASE INHIBITOR; PHASE-II TRIAL; CISPLATIN-RESISTANCE; DRUG-RESISTANCE; FGFR3; MUTATIONS; GENE; CHEMOTHERAPY;
D O I
10.1517/14728222.2014.987662
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:515 / 525
页数:11
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