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PSMA targeting in metastatic castration-resistant prostate cancer: where are we and where are we going?
Prostate-specific membrane antigen (PSMA) is highly expressed on the membrane of most prostate cancer cells and to a lesser extent in normal tissues. Many vectors targeting this protein have been created over the past decade and numerous clinical studies have positively demonstrated the tolerance an...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8554551/ https://www.ncbi.nlm.nih.gov/pubmed/34721674 http://dx.doi.org/10.1177/17588359211053898 |
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author | Giraudet, Anne-Laure Kryza, David Hofman, Michael Moreau, Aurélie Fizazi, Karim Flechon, Aude Hicks, Rodney J. Tran, Ben |
author_facet | Giraudet, Anne-Laure Kryza, David Hofman, Michael Moreau, Aurélie Fizazi, Karim Flechon, Aude Hicks, Rodney J. Tran, Ben |
author_sort | Giraudet, Anne-Laure |
collection | PubMed |
description | Prostate-specific membrane antigen (PSMA) is highly expressed on the membrane of most prostate cancer cells and to a lesser extent in normal tissues. Many vectors targeting this protein have been created over the past decade and numerous clinical studies have positively demonstrated the tolerance and efficacy of radiolabeled prostate-specific membrane antigen ligands for PSMA radioligand therapy (PRLT). Preliminary results are encouraging that PRLT will become an important addition to the current therapeutic options in a number of settings. Improvement in radiopharmaceutical targeting and combination with other oncological agents are under investigation to further improve its therapeutic efficacy. These encouraging results have led to the development of other therapies using PSMA as a target, such as PSMA–targeted chimeric antigen receptor T-cells, PSMA–targeted antibody drug conjugates, and PSMA–targeted bi-specific T-cell-directed therapy. This narrative review details the current state and advancements in prostate-specific membrane antigen targeting in prostate cancer treatment. |
format | Online Article Text |
id | pubmed-8554551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-85545512021-10-30 PSMA targeting in metastatic castration-resistant prostate cancer: where are we and where are we going? Giraudet, Anne-Laure Kryza, David Hofman, Michael Moreau, Aurélie Fizazi, Karim Flechon, Aude Hicks, Rodney J. Tran, Ben Ther Adv Med Oncol Review Prostate-specific membrane antigen (PSMA) is highly expressed on the membrane of most prostate cancer cells and to a lesser extent in normal tissues. Many vectors targeting this protein have been created over the past decade and numerous clinical studies have positively demonstrated the tolerance and efficacy of radiolabeled prostate-specific membrane antigen ligands for PSMA radioligand therapy (PRLT). Preliminary results are encouraging that PRLT will become an important addition to the current therapeutic options in a number of settings. Improvement in radiopharmaceutical targeting and combination with other oncological agents are under investigation to further improve its therapeutic efficacy. These encouraging results have led to the development of other therapies using PSMA as a target, such as PSMA–targeted chimeric antigen receptor T-cells, PSMA–targeted antibody drug conjugates, and PSMA–targeted bi-specific T-cell-directed therapy. This narrative review details the current state and advancements in prostate-specific membrane antigen targeting in prostate cancer treatment. SAGE Publications 2021-10-26 /pmc/articles/PMC8554551/ /pubmed/34721674 http://dx.doi.org/10.1177/17588359211053898 Text en © The Author(s), 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://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 page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Review Giraudet, Anne-Laure Kryza, David Hofman, Michael Moreau, Aurélie Fizazi, Karim Flechon, Aude Hicks, Rodney J. Tran, Ben PSMA targeting in metastatic castration-resistant prostate cancer: where are we and where are we going? |
title | PSMA targeting in metastatic castration-resistant prostate cancer: where are we and where are we going? |
title_full | PSMA targeting in metastatic castration-resistant prostate cancer: where are we and where are we going? |
title_fullStr | PSMA targeting in metastatic castration-resistant prostate cancer: where are we and where are we going? |
title_full_unstemmed | PSMA targeting in metastatic castration-resistant prostate cancer: where are we and where are we going? |
title_short | PSMA targeting in metastatic castration-resistant prostate cancer: where are we and where are we going? |
title_sort | psma targeting in metastatic castration-resistant prostate cancer: where are we and where are we going? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8554551/ https://www.ncbi.nlm.nih.gov/pubmed/34721674 http://dx.doi.org/10.1177/17588359211053898 |
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