Contemporary best practice in the management of urothelial carcinomas of the renal pelvis and ureter

dc.contributor.authorBianconi, Maristella
dc.contributor.authorCimadamore, Alessia
dc.contributor.authorFaloppi, Luca
dc.contributor.authorScartozzi, Mario
dc.contributor.authorSantoni, Matteo
dc.contributor.authorLopez-Beltran, Antonio
dc.contributor.authorCheng, Liang
dc.contributor.authorScarpelli, Marina
dc.contributor.authorMontironi, Rodolfo
dc.contributor.departmentPathology and Laboratory Medicine, School of Medicineen_US
dc.date.accessioned2019-07-03T15:45:43Z
dc.date.available2019-07-03T15:45:43Z
dc.date.issued2019-01-08
dc.description.abstractUpper tract urothelial carcinoma (UTUC) accounts for 5% of urothelial carcinomas (UCs), the estimated annual incidence being 1-2 cases per 100,000 inhabitants. Similarly to bladder UC, divergent differentiations and histologic variants confer an adverse risk factor in comparison with pure UTUC. Molecular and genomic characterization studies on UTUC have shown changes occurring at differing frequencies from bladder cancer, with unique molecular and clinical subtypes, potentially with different responses to treatment. Systemic chemotherapy is the standard approach for patients with inoperable locally advanced or metastatic UCs. Although initial response rates are high, the median survival with combination chemotherapy is about 15 months. In first-line chemotherapy several cisplatin-based regimens have been proposed. For patients with advanced UC who progress to first-line treatment, the only product licensed in Europe is vinflunine, a third-generation, semisynthetic, vinca alkaloid. Better response rates (15-60%), with higher toxicity rates and no overall survival (OS) benefit, are generally achieved in multidrug combinations, which often include taxanes and gemcitabine. The US FDA has recently approved five agents targeting the programmed death-1 and programmed death ligand-1 pathway as a second-line therapy in patients with locally advanced or metastatic UC with disease progression during or following platinum-containing chemotherapy. Potential therapeutic targets are present in 69% of tumours analyzed. Specific molecular alterations include those involved in the RTK/Ras/PI(3)K, cell-cycle regulation and chromatin-remodeling pathways, many of them have either targeted therapies approved or under investigation. Angiogenic agents, anti-epidermal growth factor receptor therapy, phosphoinositide 3-kinase (PI3K) and mammalian target of rapamycin (mTOR) pathway inhibitors and immunotherapeutic drugs are being successfully investigated.en_US
dc.identifier.citationBianconi, M., Cimadamore, A., Faloppi, L., Scartozzi, M., Santoni, M., Lopez-Beltran, A., … Montironi, R. (2019). Contemporary best practice in the management of urothelial carcinomas of the renal pelvis and ureter. Therapeutic advances in urology, 11, 1756287218815372. doi:10.1177/1756287218815372en_US
dc.identifier.urihttps://hdl.handle.net/1805/19824
dc.language.isoen_USen_US
dc.publisherSageen_US
dc.relation.isversionof10.1177/1756287218815372en_US
dc.relation.journalTherapeutic Advances in Urologyen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.sourcePMCen_US
dc.subjectAntiangiogenic agentsen_US
dc.subjectChemotherapyen_US
dc.subjectGene expression profilingen_US
dc.subjectImmunotherapyen_US
dc.subjectTarget therapiesen_US
dc.subjectUpper urinary tracten_US
dc.subjectUrothelial carcinomaen_US
dc.titleContemporary best practice in the management of urothelial carcinomas of the renal pelvis and ureteren_US
dc.typeArticleen_US
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