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Advancements in Therapy for Bladder Cancer: Enfortumab Vedotin
The treatment paradigm for urothelial carcinoma (UC), a common genitourinary cancer, has significantly expanded in recent years. Enfortumab vedotin, a Nectin-4–targeted antibody-drug conjugate, was recently approved by the U.S. Food & Drug Administration for patients with advanced or metastatic...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Harborside Press LLC
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7863123/ https://www.ncbi.nlm.nih.gov/pubmed/33604101 http://dx.doi.org/10.6004/jadpro.2020.11.4.8 |
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author | Hanna, Kirollos S. |
author_facet | Hanna, Kirollos S. |
author_sort | Hanna, Kirollos S. |
collection | PubMed |
description | The treatment paradigm for urothelial carcinoma (UC), a common genitourinary cancer, has significantly expanded in recent years. Enfortumab vedotin, a Nectin-4–targeted antibody-drug conjugate, was recently approved by the U.S. Food & Drug Administration for patients with advanced or metastatic UC following chemotherapy and immunotherapy. Approval of enfortumab vedotin was based on findings from the EV-201 trial, which demonstrated objective response rates of 44%. Patients treated with enfortumab vedotin should be monitored for specific toxicities, including peripheral neuropathy, rash, and hyperglycemia. In this article, the clinical implications of enfortumab vedotin for the treatment of advanced UC are reviewed. |
format | Online Article Text |
id | pubmed-7863123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Harborside Press LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-78631232021-02-17 Advancements in Therapy for Bladder Cancer: Enfortumab Vedotin Hanna, Kirollos S. J Adv Pract Oncol Prescriber’s Corner The treatment paradigm for urothelial carcinoma (UC), a common genitourinary cancer, has significantly expanded in recent years. Enfortumab vedotin, a Nectin-4–targeted antibody-drug conjugate, was recently approved by the U.S. Food & Drug Administration for patients with advanced or metastatic UC following chemotherapy and immunotherapy. Approval of enfortumab vedotin was based on findings from the EV-201 trial, which demonstrated objective response rates of 44%. Patients treated with enfortumab vedotin should be monitored for specific toxicities, including peripheral neuropathy, rash, and hyperglycemia. In this article, the clinical implications of enfortumab vedotin for the treatment of advanced UC are reviewed. Harborside Press LLC 2020 2020-05-01 /pmc/articles/PMC7863123/ /pubmed/33604101 http://dx.doi.org/10.6004/jadpro.2020.11.4.8 Text en © 2020 Harborside™ http://creativecommons.org/licenses/by-nc-nd/3.0/ This article is distributed under the terms of the Creative Commons Attribution Non-Commercial Non-Derivative License, which permits unrestricted non-commercial and non-derivative use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Prescriber’s Corner Hanna, Kirollos S. Advancements in Therapy for Bladder Cancer: Enfortumab Vedotin |
title | Advancements in Therapy for Bladder Cancer: Enfortumab Vedotin |
title_full | Advancements in Therapy for Bladder Cancer: Enfortumab Vedotin |
title_fullStr | Advancements in Therapy for Bladder Cancer: Enfortumab Vedotin |
title_full_unstemmed | Advancements in Therapy for Bladder Cancer: Enfortumab Vedotin |
title_short | Advancements in Therapy for Bladder Cancer: Enfortumab Vedotin |
title_sort | advancements in therapy for bladder cancer: enfortumab vedotin |
topic | Prescriber’s Corner |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7863123/ https://www.ncbi.nlm.nih.gov/pubmed/33604101 http://dx.doi.org/10.6004/jadpro.2020.11.4.8 |
work_keys_str_mv | AT hannakirolloss advancementsintherapyforbladdercancerenfortumabvedotin |