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Systemic Immunotherapy for Urothelial Cancer: Current Trends and Future Directions
Urothelial cancer of the bladder, renal pelvis, ureter, and other urinary organs is the fifth most common cancer in the United States, and systemic platinum-based chemotherapy remains the standard of care for first-line treatment of advanced/metastatic urothelial carcinoma (UC). Until recently, ther...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5332938/ https://www.ncbi.nlm.nih.gov/pubmed/28134806 http://dx.doi.org/10.3390/cancers9020015 |
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author | Gupta, Shilpa Gill, David Poole, Austin Agarwal, Neeraj |
author_facet | Gupta, Shilpa Gill, David Poole, Austin Agarwal, Neeraj |
author_sort | Gupta, Shilpa |
collection | PubMed |
description | Urothelial cancer of the bladder, renal pelvis, ureter, and other urinary organs is the fifth most common cancer in the United States, and systemic platinum-based chemotherapy remains the standard of care for first-line treatment of advanced/metastatic urothelial carcinoma (UC). Until recently, there were very limited options for patients who are refractory to chemotherapy, or do not tolerate chemotherapy due to toxicities and overall outcomes have remained very poor. While the role of immunotherapy was first established in non-muscle invasive bladder cancer in the 1970s, no systemic immunotherapy was approved for advanced disease until the recent approval of a programmed death ligand-1 (PD-L1) inhibitor, atezolizumab, in patients with advanced/metastatic UC who have progressed on platinum-containing regimens. This represents a significant milestone in this disease after a void of over 30 years. In addition to atezolizumab, a variety of checkpoint inhibitors have shown a significant activity in advanced/metastatic urothelial carcinoma and are expected to gain Food and Drug Administration (FDA) approval in the near future. The introduction of novel immunotherapy agents has led to rapid changes in the field of urothelial carcinoma. Numerous checkpoint inhibitors are being tested alone or in combination in the first and subsequent-line therapies of metastatic disease, as well as neoadjuvant and adjuvant settings. They are also being studied in combination with radiation therapy and for non-muscle invasive bladder cancer refractory to BCG. Furthermore, immunotherapy is being utilized for those ineligible for first-line platinum-based chemotherapy. This review outlines the novel immunotherapy agents which have either been approved, or are currently being investigated in clinical trials in UC. |
format | Online Article Text |
id | pubmed-5332938 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-53329382017-03-13 Systemic Immunotherapy for Urothelial Cancer: Current Trends and Future Directions Gupta, Shilpa Gill, David Poole, Austin Agarwal, Neeraj Cancers (Basel) Review Urothelial cancer of the bladder, renal pelvis, ureter, and other urinary organs is the fifth most common cancer in the United States, and systemic platinum-based chemotherapy remains the standard of care for first-line treatment of advanced/metastatic urothelial carcinoma (UC). Until recently, there were very limited options for patients who are refractory to chemotherapy, or do not tolerate chemotherapy due to toxicities and overall outcomes have remained very poor. While the role of immunotherapy was first established in non-muscle invasive bladder cancer in the 1970s, no systemic immunotherapy was approved for advanced disease until the recent approval of a programmed death ligand-1 (PD-L1) inhibitor, atezolizumab, in patients with advanced/metastatic UC who have progressed on platinum-containing regimens. This represents a significant milestone in this disease after a void of over 30 years. In addition to atezolizumab, a variety of checkpoint inhibitors have shown a significant activity in advanced/metastatic urothelial carcinoma and are expected to gain Food and Drug Administration (FDA) approval in the near future. The introduction of novel immunotherapy agents has led to rapid changes in the field of urothelial carcinoma. Numerous checkpoint inhibitors are being tested alone or in combination in the first and subsequent-line therapies of metastatic disease, as well as neoadjuvant and adjuvant settings. They are also being studied in combination with radiation therapy and for non-muscle invasive bladder cancer refractory to BCG. Furthermore, immunotherapy is being utilized for those ineligible for first-line platinum-based chemotherapy. This review outlines the novel immunotherapy agents which have either been approved, or are currently being investigated in clinical trials in UC. MDPI 2017-01-27 /pmc/articles/PMC5332938/ /pubmed/28134806 http://dx.doi.org/10.3390/cancers9020015 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Gupta, Shilpa Gill, David Poole, Austin Agarwal, Neeraj Systemic Immunotherapy for Urothelial Cancer: Current Trends and Future Directions |
title | Systemic Immunotherapy for Urothelial Cancer: Current Trends and Future Directions |
title_full | Systemic Immunotherapy for Urothelial Cancer: Current Trends and Future Directions |
title_fullStr | Systemic Immunotherapy for Urothelial Cancer: Current Trends and Future Directions |
title_full_unstemmed | Systemic Immunotherapy for Urothelial Cancer: Current Trends and Future Directions |
title_short | Systemic Immunotherapy for Urothelial Cancer: Current Trends and Future Directions |
title_sort | systemic immunotherapy for urothelial cancer: current trends and future directions |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5332938/ https://www.ncbi.nlm.nih.gov/pubmed/28134806 http://dx.doi.org/10.3390/cancers9020015 |
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