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Open AccessJournal ArticleDOI

A place for precision medicine in bladder cancer: targeting the FGFRs

TLDR
Current understanding of the molecular alterations affecting these receptors in bladder tumors, preclinical studies validating them as therapeutic targets, available FGFR-targeted agents and results from early clinical trials in bladder cancer patients are summarized.
Abstract
Bladder tumors show diverse molecular features and clinical outcome. Muscle-invasive bladder cancer has poor prognosis and novel approaches to systemic therapy are urgently required. Non-muscle-invasive bladder cancer has good prognosis, but high recurrence rate and the requirement for life-long disease monitoring places a major burden on patients and healthcare providers. Studies of tumor tissues from both disease groups have identified frequent alterations of FGFRs, including mutations of FGFR3 and dysregulated expression of FGFR1 and FGFR3 that suggest that these may be valid therapeutic targets. We summarize current understanding of the molecular alterations affecting these receptors in bladder tumors, preclinical studies validating them as therapeutic targets, available FGFR-targeted agents and results from early clinical trials in bladder cancer patients.

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Journal ArticleDOI

Advances in bladder cancer biology and therapy

TL;DR: Recent developments in the molecular and translational aspects of bladder cancer biology are examined and their current or potential future clinical applications in the management of bladdercancer are discussed.
Journal ArticleDOI

Fibroblast growth factor receptors as treatment targets in clinical oncology

TL;DR: The clinical experience with FGFR inhibitors to date is described, and key aspects that might lead to improved response rates and/or the avoidance of acquired resistance are highlighted, including the selection of patients who are most likely to benefit from treatment, and the use ofFGFR inhibitors in combination regimens with other agents.
Journal ArticleDOI

Targeted therapies for advanced bladder cancer: new strategies with FGFR inhibitors:

TL;DR: An overview of the results of recent clinical trials on FGFR tyrosine kinase inhibitors currently in clinical development for the treatment of UC, and future therapeutic options of combination regimens with immune-checkpoint inhibitors as strategies for improving the antitumor effects of this class of drug.
Journal ArticleDOI

Connecting the dots between different networks: miRNAs associated with bladder cancer risk and progression.

TL;DR: Altered miRNAs patterns are interrelated to bladder tumorigenesis, allowing them to be used for the development of novel diagnostic and prognostic biomarkers, and can assist for better patient diagnosis.
References
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Journal ArticleDOI

Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008.

TL;DR: The results for 20 world regions are presented, summarizing the global patterns for the eight most common cancers, and striking differences in the patterns of cancer from region to region are observed.
Journal ArticleDOI

Cancer drug resistance: an evolving paradigm

TL;DR: There are now unprecedented opportunities to understand and overcome drug resistance through the clinical assessment of rational therapeutic drug combinations and the use of predictive biomarkers to enable patient stratification.
Journal ArticleDOI

Predicting recurrence and progression in individual patients with stage Ta T1 bladder cancer using EORTC risk tables: a combined analysis of 2596 patients from seven EORTC trials.

TL;DR: These probabilities allow urologists to easily calculate a superficial bladder cancer patient's short- and long-term risks of recurrence and progression after transurethral resection to determine the most appropriate treatment and frequency of follow-up.
Journal ArticleDOI

Comprehensive molecular characterization of urothelial bladder carcinoma

John N. Weinstein, +296 more
- 01 Jan 2014 - 
TL;DR: Ch Chromatin regulatory genes were more frequently mutated in urothelial carcinoma than in any other common cancer studied so far, indicating the future possibility of targeted therapy for chromatin abnormalities.
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