TY - JOUR
T1 - Novel molecular targets for the therapy of urothelial carcinoma
AU - Jana, Bagi R.P.
AU - Galsky, Matthew D.
AU - Hahn, Noah M.
AU - Milowsky, Matthew I.
AU - Sonpavde, Guru
N1 - Funding Information:
BRP Jana is a speaker for Sanofi-Aventis and Amgen. MD Galsky is on the advisory board for GSK, BMS, Pfizer, Amgen and Aveo. He has received research funding from Cel-gene and Novartis. NM Hahn is a speaker for Sanofi-Aventis and Janssen; he has received research support from Bristol-Myers Squibb, Genentech, Novartis and Celgene. G Sonpavde has received research support from Novartis, BMS, Celgene and Teva. He is a speaker for GSK, Novartis, Sanofi-Aventis, Janssen and Amgen.
Copyright:
Copyright 2014 Elsevier B.V., All rights reserved.
PY - 2012/5
Y1 - 2012/5
N2 - Introduction: First-line platinum-based combinations are active in locally advanced and metastatic urothelial carcinoma; however, long-term outcomes including disease-specific and overall survival remain suboptimal. In addition, approximately 40 50% of patients with advanced urothelial carcinoma have coexisting medical issues that preclude the use of cisplatin-based therapy. Improvements in our understanding of the molecular mechanisms of urothelial tumorigenesis have led to first-generation clinical trials evaluating novel agents targeting molecular pathways. These are particularly relevant in regard to subpopulations. Novel trial designs warrant consideration to accelerate accrual. Areas covered: In this review, novel molecular targets for the therapy of urothelial carcinoma, as well as recently completed and ongoing clinical trials utilizing novel targeted agents, are discussed. A Medline search with key words, abstracts reported at national conferences on urothelial carcinoma and NCI clinical trial identifiers was used for this review. Expert opinion: Improved understanding of molecular biology has identified a number of new molecular targets, but there is a seeming absence of one dominant molecular driver for urothelial cancer. An adaptive and biomarker-derived strategy may be warranted. Clinical trials utilizing targeted agents are ongoing and results are awaited.
AB - Introduction: First-line platinum-based combinations are active in locally advanced and metastatic urothelial carcinoma; however, long-term outcomes including disease-specific and overall survival remain suboptimal. In addition, approximately 40 50% of patients with advanced urothelial carcinoma have coexisting medical issues that preclude the use of cisplatin-based therapy. Improvements in our understanding of the molecular mechanisms of urothelial tumorigenesis have led to first-generation clinical trials evaluating novel agents targeting molecular pathways. These are particularly relevant in regard to subpopulations. Novel trial designs warrant consideration to accelerate accrual. Areas covered: In this review, novel molecular targets for the therapy of urothelial carcinoma, as well as recently completed and ongoing clinical trials utilizing novel targeted agents, are discussed. A Medline search with key words, abstracts reported at national conferences on urothelial carcinoma and NCI clinical trial identifiers was used for this review. Expert opinion: Improved understanding of molecular biology has identified a number of new molecular targets, but there is a seeming absence of one dominant molecular driver for urothelial cancer. An adaptive and biomarker-derived strategy may be warranted. Clinical trials utilizing targeted agents are ongoing and results are awaited.
KW - Novel molecular targets
KW - Targeted therapy
KW - Transitional cell carcinoma
KW - Urothelial carcinoma
UR - http://www.scopus.com/inward/record.url?scp=84860254010&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84860254010&partnerID=8YFLogxK
U2 - 10.1517/14728222.2012.677441
DO - 10.1517/14728222.2012.677441
M3 - Review article
C2 - 22510032
AN - SCOPUS:84860254010
SN - 1472-8222
VL - 16
SP - 499
EP - 513
JO - Expert Opinion on Therapeutic Targets
JF - Expert Opinion on Therapeutic Targets
IS - 5
ER -