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Contemporary best practice in the management of urothelial carcinomas of the renal pelvis and ureter
Upper 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. Mole...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329040/ https://www.ncbi.nlm.nih.gov/pubmed/30671136 http://dx.doi.org/10.1177/1756287218815372 |
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author | Bianconi, Maristella Cimadamore, Alessia Faloppi, Luca Scartozzi, Mario Santoni, Matteo Lopez-Beltran, Antonio Cheng, Liang Scarpelli, Marina Montironi, Rodolfo |
author_facet | Bianconi, Maristella Cimadamore, Alessia Faloppi, Luca Scartozzi, Mario Santoni, Matteo Lopez-Beltran, Antonio Cheng, Liang Scarpelli, Marina Montironi, Rodolfo |
author_sort | Bianconi, Maristella |
collection | PubMed |
description | Upper 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. |
format | Online Article Text |
id | pubmed-6329040 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-63290402019-01-22 Contemporary best practice in the management of urothelial carcinomas of the renal pelvis and ureter Bianconi, Maristella Cimadamore, Alessia Faloppi, Luca Scartozzi, Mario Santoni, Matteo Lopez-Beltran, Antonio Cheng, Liang Scarpelli, Marina Montironi, Rodolfo Ther Adv Urol Review Upper 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. SAGE Publications 2019-01-08 /pmc/articles/PMC6329040/ /pubmed/30671136 http://dx.doi.org/10.1177/1756287218815372 Text en © The Author(s), 2019 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Review Bianconi, Maristella Cimadamore, Alessia Faloppi, Luca Scartozzi, Mario Santoni, Matteo Lopez-Beltran, Antonio Cheng, Liang Scarpelli, Marina Montironi, Rodolfo Contemporary best practice in the management of urothelial carcinomas of the renal pelvis and ureter |
title | Contemporary best practice in the management of urothelial carcinomas of the renal pelvis and ureter |
title_full | Contemporary best practice in the management of urothelial carcinomas of the renal pelvis and ureter |
title_fullStr | Contemporary best practice in the management of urothelial carcinomas of the renal pelvis and ureter |
title_full_unstemmed | Contemporary best practice in the management of urothelial carcinomas of the renal pelvis and ureter |
title_short | Contemporary best practice in the management of urothelial carcinomas of the renal pelvis and ureter |
title_sort | contemporary best practice in the management of urothelial carcinomas of the renal pelvis and ureter |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329040/ https://www.ncbi.nlm.nih.gov/pubmed/30671136 http://dx.doi.org/10.1177/1756287218815372 |
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