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Merck

Cytotoxic and DNA-targeted therapy in urothelial cancer: have we squeezed the lemon enough?

Cancer (2014-08-06)
Arjun V Balar, Matthew I Milowsky
RESUMEN

Urothelial cancer has long been known as a chemotherapy-sensitive disease. However, clinical trial data to date suggest a plateau to the magnitude of benefit from cytotoxic therapy alone. In spite of level 1 evidence supporting cisplatin-based chemotherapy for patients with muscle-invasive and metastatic urothelial cancer, underuse prevails among patients with localized disease and only a modest survival benefit exists in the metastatic setting, although trials have consistently demonstrated that there is a subset of patients who clearly benefit. Recent comprehensive genomic profiling has identified a high prevalence of actionable genomic alterations as well as other potential targets yet to be fully understood. Modern clinical trials must now focus on identifying predictive biomarkers to select those patients who will benefit most from cytotoxic chemotherapy, molecularly targeted therapy, or potentially both.

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Sigma-Aldrich
Metotrexato hydrate, ≥98% (HPLC), powder
Sigma-Aldrich
Metotrexato hydrate, powder, BioReagent, suitable for cell culture, ≥98% (HPLC)
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Metotrexato hydrate, meets USP testing specifications
SAFC
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Methotrexate solution, 1.0 mg/mL in methanol with 0.1N NaOH, ampule of 1 mL, certified reference material, Cerilliant®
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Metotrexato hydrate, ≥99.0% (sum of enantiomers, HPLC)
Methotrexate for peak identification, European Pharmacopoeia (EP) Reference Standard
Methotrexate for system suitability, European Pharmacopoeia (EP) Reference Standard