TitleNovel molecular targets for urothelial carcinoma
Publication TypeJournal Article
Year of Publication2015
AuthorsFaltas BM, Karir BS, Tagawa ST, Rosenberg JE
JournalExpert Opin Ther Targets
Volume19
Issue4
Pagination515-25
Date Published2015 Apr
ISSN1744-7631
KeywordsAnimals, Antineoplastic Agents, Carcinoma, Transitional Cell, Drug Approval, Drug Design, Drug Resistance, Neoplasm, Humans, Molecular Targeted Therapy, United States, United States Food and Drug Administration, Urothelium
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.

DOI10.1517/14728222.2014.987662
Alternate JournalExpert Opin. Ther. Targets
PubMed ID25633079
PubMed Central IDPMC4406627
Grant ListKL2 TR000458 / TR / NCATS NIH HHS / United States
P30 CA008748 / CA / NCI NIH HHS / United States
KL2TR000458 / TR / NCATS NIH HHS / United States