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Antibody-Drug Conjugates in Bladder Cancer
Urothelial carcinoma (UC) is characterized by expression of a plethora of cell surface antigens, thus offering opportunities for specific therapeutic targeting with use of antibody-drug conjugates (ADCs). ADCs are structured from two major constituents, a monoclonal antibody (mAb) against a specific...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6087439/ https://www.ncbi.nlm.nih.gov/pubmed/30112436 http://dx.doi.org/10.3233/BLC-180169 |
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author | Vlachostergios, Panagiotis J. Jakubowski, Christopher D. Niaz, Muhammad J. Lee, Aileen Thomas, Charlene Hackett, Amy L. Patel, Priyanka Rashid, Naureen Tagawa, Scott T. |
author_facet | Vlachostergios, Panagiotis J. Jakubowski, Christopher D. Niaz, Muhammad J. Lee, Aileen Thomas, Charlene Hackett, Amy L. Patel, Priyanka Rashid, Naureen Tagawa, Scott T. |
author_sort | Vlachostergios, Panagiotis J. |
collection | PubMed |
description | Urothelial carcinoma (UC) is characterized by expression of a plethora of cell surface antigens, thus offering opportunities for specific therapeutic targeting with use of antibody-drug conjugates (ADCs). ADCs are structured from two major constituents, a monoclonal antibody (mAb) against a specific target and a cytotoxic drug connected via a linker molecule. Several ADCs are developed against different UC surface markers, but the ones at most advanced stages of development include sacituzumab govitecan (IMMU-132), enfortumab vedotin (ASG-22CE/ASG-22ME), ASG-15ME for advanced UC, and oportuzumab monatox (VB4-845) for early UC. Several new targets are identified and utilized for novel or existing ADC testing. The most promising ones include human epidermal growth factor receptor 2 (HER2) and members of the fibroblast growth factor receptor axis (FGF/FGFR). Positive preclinical and early clinical results are reported in many cases, thus the next step involves further improving efficacy and reducing toxicity as well as testing combination strategies with approved agents. |
format | Online Article Text |
id | pubmed-6087439 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | IOS Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-60874392018-08-13 Antibody-Drug Conjugates in Bladder Cancer Vlachostergios, Panagiotis J. Jakubowski, Christopher D. Niaz, Muhammad J. Lee, Aileen Thomas, Charlene Hackett, Amy L. Patel, Priyanka Rashid, Naureen Tagawa, Scott T. Bladder Cancer Review Urothelial carcinoma (UC) is characterized by expression of a plethora of cell surface antigens, thus offering opportunities for specific therapeutic targeting with use of antibody-drug conjugates (ADCs). ADCs are structured from two major constituents, a monoclonal antibody (mAb) against a specific target and a cytotoxic drug connected via a linker molecule. Several ADCs are developed against different UC surface markers, but the ones at most advanced stages of development include sacituzumab govitecan (IMMU-132), enfortumab vedotin (ASG-22CE/ASG-22ME), ASG-15ME for advanced UC, and oportuzumab monatox (VB4-845) for early UC. Several new targets are identified and utilized for novel or existing ADC testing. The most promising ones include human epidermal growth factor receptor 2 (HER2) and members of the fibroblast growth factor receptor axis (FGF/FGFR). Positive preclinical and early clinical results are reported in many cases, thus the next step involves further improving efficacy and reducing toxicity as well as testing combination strategies with approved agents. IOS Press 2018-07-30 /pmc/articles/PMC6087439/ /pubmed/30112436 http://dx.doi.org/10.3233/BLC-180169 Text en © 2018 – IOS Press and the authors. All rights reserved https://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Vlachostergios, Panagiotis J. Jakubowski, Christopher D. Niaz, Muhammad J. Lee, Aileen Thomas, Charlene Hackett, Amy L. Patel, Priyanka Rashid, Naureen Tagawa, Scott T. Antibody-Drug Conjugates in Bladder Cancer |
title | Antibody-Drug Conjugates in Bladder Cancer |
title_full | Antibody-Drug Conjugates in Bladder Cancer |
title_fullStr | Antibody-Drug Conjugates in Bladder Cancer |
title_full_unstemmed | Antibody-Drug Conjugates in Bladder Cancer |
title_short | Antibody-Drug Conjugates in Bladder Cancer |
title_sort | antibody-drug conjugates in bladder cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6087439/ https://www.ncbi.nlm.nih.gov/pubmed/30112436 http://dx.doi.org/10.3233/BLC-180169 |
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