Recent advances in molecular biology and drug design have described novel targets in bladder cancer. EGFR, fibroblast growth factor receptor (FGFR), VEGFR, phosphoinositide 3-kinase (PI3K)/AKT/mammalian target of rapamycin (mTOR) pathway, PD-1, cyclooxygenase 2 (COX-2), Aurora kinase A, and miRNA are just examples of these opening frontiers. In addition, epithelial to mesenchymal transition (EMT) and cancer stem cells (CSCs) are promising candidates for future therapeutic approaches. Novel agents, combination, and sequences are emerging from the 747 clinical studies presently in course in bladder cancer to optimize patient outcomes. This report describes the emerging targets and provides an update on ongoing phase I, II, and III trials and preliminary results on targeted agents, used alone, in sequences, or in combination for patients with bladder cancer.

The route to personalized medicine in bladder cancer: where do we stand? / Massari, F; Ciccarese, C; Santoni, M; Brunelli, M; Conti, A; Modena, A; Montironi, R; Santini, D; Cheng, L; Martignoni, G; Cascinu, S; Tortora, G.. - In: TARGETED ONCOLOGY. - ISSN 1776-2596. - (2015).

The route to personalized medicine in bladder cancer: where do we stand?

Santini D;
2015

Abstract

Recent advances in molecular biology and drug design have described novel targets in bladder cancer. EGFR, fibroblast growth factor receptor (FGFR), VEGFR, phosphoinositide 3-kinase (PI3K)/AKT/mammalian target of rapamycin (mTOR) pathway, PD-1, cyclooxygenase 2 (COX-2), Aurora kinase A, and miRNA are just examples of these opening frontiers. In addition, epithelial to mesenchymal transition (EMT) and cancer stem cells (CSCs) are promising candidates for future therapeutic approaches. Novel agents, combination, and sequences are emerging from the 747 clinical studies presently in course in bladder cancer to optimize patient outcomes. This report describes the emerging targets and provides an update on ongoing phase I, II, and III trials and preliminary results on targeted agents, used alone, in sequences, or in combination for patients with bladder cancer.
2015
01 Pubblicazione su rivista::01a Articolo in rivista
The route to personalized medicine in bladder cancer: where do we stand? / Massari, F; Ciccarese, C; Santoni, M; Brunelli, M; Conti, A; Modena, A; Montironi, R; Santini, D; Cheng, L; Martignoni, G; Cascinu, S; Tortora, G.. - In: TARGETED ONCOLOGY. - ISSN 1776-2596. - (2015).
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1642256
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