Cargando…

Treatment Options for Metastatic Urothelial Carcinoma After First-Line Chemotherapy

Urothelial carcinoma (UC) is a frequently diagnosed tumor and an important cause of cancer deaths worldwide. Until a few years ago, despite the unquestioned role of platinum-based chemotherapy, therapeutic choices beyond the first line were limited and related to unsatisfactory outcomes. Metastatic...

Descripción completa

Detalles Bibliográficos
Autores principales: Tassinari, Elisa, Mollica, Veronica, Nuvola, Giacomo, Marchetti, Andrea, Rosellini, Matteo, Massari, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9205436/
https://www.ncbi.nlm.nih.gov/pubmed/35720644
http://dx.doi.org/10.2147/CMAR.S287904
_version_ 1784729131109318656
author Tassinari, Elisa
Mollica, Veronica
Nuvola, Giacomo
Marchetti, Andrea
Rosellini, Matteo
Massari, Francesco
author_facet Tassinari, Elisa
Mollica, Veronica
Nuvola, Giacomo
Marchetti, Andrea
Rosellini, Matteo
Massari, Francesco
author_sort Tassinari, Elisa
collection PubMed
description Urothelial carcinoma (UC) is a frequently diagnosed tumor and an important cause of cancer deaths worldwide. Until a few years ago, despite the unquestioned role of platinum-based chemotherapy, therapeutic choices beyond the first line were limited and related to unsatisfactory outcomes. Metastatic UC has always been associated with a poor prognosis, with overall survival only slightly above a year. In the recent past, huge progress has been made in our understanding of the molecular and genomic disease characteristics, to enable stratification of patients in terms of prognosis and treatment responses. Unfortunately, we still do not have the perfect combination of clinical biomarkers to tailor the optimal treatment for each patient, despite making several efforts in this direction. The therapeutic arsenal has been augmented by immune checkpoint inhibitors (ICIs), which nowadays represent the backbone of the second-line setting. Equally revolutionary was the FDA’s approval of erdafitinib, a potent fibroblast growth factor receptor (FGFR) inhibitor, the use of which is reserved for patients whose tumor harbors specific FGF pathway alterations. Recently, the therapeutic landscape of metastatic UC has been enhanced by the introduction of novel compounds, consisting of antibody–drug conjugates (ADCs). Enfortumab vedotin is an antibody targeting nectin-4, a cell adhesion molecule highly expressed in UC, conjugated to monomethyl auristatin E (MMAE), a microtubule-disrupting agent. Sacituzumab govitecan is a humanized monoclonal antibody targeting Trop-2, a transmembrane glycoprotein, conjugated to the active metabolite of irinotecan. These two compounds have received accelerated approval by the FDA in patients pretreated with platinum-based chemotherapy and immunotherapy. Several ongoing trials are investigating the role of ICIs combined with chemotherapy, antiangiogenic drugs, or other ICIs, as well as the efficacy of PARP inhibitors and target therapies, hoping to provide information for some important unmet needs. In this review, we aim to evaluate the current potential treatment options after first-line chemotherapy.
format Online
Article
Text
id pubmed-9205436
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Dove
record_format MEDLINE/PubMed
spelling pubmed-92054362022-06-18 Treatment Options for Metastatic Urothelial Carcinoma After First-Line Chemotherapy Tassinari, Elisa Mollica, Veronica Nuvola, Giacomo Marchetti, Andrea Rosellini, Matteo Massari, Francesco Cancer Manag Res Review Urothelial carcinoma (UC) is a frequently diagnosed tumor and an important cause of cancer deaths worldwide. Until a few years ago, despite the unquestioned role of platinum-based chemotherapy, therapeutic choices beyond the first line were limited and related to unsatisfactory outcomes. Metastatic UC has always been associated with a poor prognosis, with overall survival only slightly above a year. In the recent past, huge progress has been made in our understanding of the molecular and genomic disease characteristics, to enable stratification of patients in terms of prognosis and treatment responses. Unfortunately, we still do not have the perfect combination of clinical biomarkers to tailor the optimal treatment for each patient, despite making several efforts in this direction. The therapeutic arsenal has been augmented by immune checkpoint inhibitors (ICIs), which nowadays represent the backbone of the second-line setting. Equally revolutionary was the FDA’s approval of erdafitinib, a potent fibroblast growth factor receptor (FGFR) inhibitor, the use of which is reserved for patients whose tumor harbors specific FGF pathway alterations. Recently, the therapeutic landscape of metastatic UC has been enhanced by the introduction of novel compounds, consisting of antibody–drug conjugates (ADCs). Enfortumab vedotin is an antibody targeting nectin-4, a cell adhesion molecule highly expressed in UC, conjugated to monomethyl auristatin E (MMAE), a microtubule-disrupting agent. Sacituzumab govitecan is a humanized monoclonal antibody targeting Trop-2, a transmembrane glycoprotein, conjugated to the active metabolite of irinotecan. These two compounds have received accelerated approval by the FDA in patients pretreated with platinum-based chemotherapy and immunotherapy. Several ongoing trials are investigating the role of ICIs combined with chemotherapy, antiangiogenic drugs, or other ICIs, as well as the efficacy of PARP inhibitors and target therapies, hoping to provide information for some important unmet needs. In this review, we aim to evaluate the current potential treatment options after first-line chemotherapy. Dove 2022-06-13 /pmc/articles/PMC9205436/ /pubmed/35720644 http://dx.doi.org/10.2147/CMAR.S287904 Text en © 2022 Tassinari et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Review
Tassinari, Elisa
Mollica, Veronica
Nuvola, Giacomo
Marchetti, Andrea
Rosellini, Matteo
Massari, Francesco
Treatment Options for Metastatic Urothelial Carcinoma After First-Line Chemotherapy
title Treatment Options for Metastatic Urothelial Carcinoma After First-Line Chemotherapy
title_full Treatment Options for Metastatic Urothelial Carcinoma After First-Line Chemotherapy
title_fullStr Treatment Options for Metastatic Urothelial Carcinoma After First-Line Chemotherapy
title_full_unstemmed Treatment Options for Metastatic Urothelial Carcinoma After First-Line Chemotherapy
title_short Treatment Options for Metastatic Urothelial Carcinoma After First-Line Chemotherapy
title_sort treatment options for metastatic urothelial carcinoma after first-line chemotherapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9205436/
https://www.ncbi.nlm.nih.gov/pubmed/35720644
http://dx.doi.org/10.2147/CMAR.S287904
work_keys_str_mv AT tassinarielisa treatmentoptionsformetastaticurothelialcarcinomaafterfirstlinechemotherapy
AT mollicaveronica treatmentoptionsformetastaticurothelialcarcinomaafterfirstlinechemotherapy
AT nuvolagiacomo treatmentoptionsformetastaticurothelialcarcinomaafterfirstlinechemotherapy
AT marchettiandrea treatmentoptionsformetastaticurothelialcarcinomaafterfirstlinechemotherapy
AT rosellinimatteo treatmentoptionsformetastaticurothelialcarcinomaafterfirstlinechemotherapy
AT massarifrancesco treatmentoptionsformetastaticurothelialcarcinomaafterfirstlinechemotherapy