Cargando…
Prostate-Specific Membrane Antigen-Based Therapeutics
Prostate cancer (PC) is the most common noncutaneous malignancy affecting men in the US, leading to significant morbidity and mortality. While significant therapeutic advances have been made, available systemic therapeutic options are lacking. Prostate-specific membrane antigen (PSMA) is a highly-re...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3145341/ https://www.ncbi.nlm.nih.gov/pubmed/21811498 http://dx.doi.org/10.1155/2012/973820 |
_version_ | 1782209084982820864 |
---|---|
author | Akhtar, Naveed H. Pail, Orrin Saran, Ankeeta Tyrell, Lauren Tagawa, Scott T. |
author_facet | Akhtar, Naveed H. Pail, Orrin Saran, Ankeeta Tyrell, Lauren Tagawa, Scott T. |
author_sort | Akhtar, Naveed H. |
collection | PubMed |
description | Prostate cancer (PC) is the most common noncutaneous malignancy affecting men in the US, leading to significant morbidity and mortality. While significant therapeutic advances have been made, available systemic therapeutic options are lacking. Prostate-specific membrane antigen (PSMA) is a highly-restricted prostate cell-surface antigen that may be targeted. While initial anti-PSMA monoclonal antibodies were suboptimal, the development of monoclonal antibodies such as J591 which are highly specific for the external domain of PSMA has allowed targeting of viable, intact prostate cancer cells. Radiolabeled J591 has demonstrated accurate and selective tumor targeting, safety, and efficacy. Ongoing studies using anti-PSMA radioimmunotherapy with (177)Lu-J591 seek to improve the therapeutic profile, select optimal candidates with biomarkers, combine with chemotherapy, and prevent or delay the onset of metastatic disease for men with biochemical relapse. Anti-PSMA monoclonal antibody-drug conjugates have also been developed with completed and ongoing early-phase clinical trials. As PSMA is a selective antigen that is highly overexpressed in prostate cancer, anti-PSMA-based immunotherapy has also been studied and utilized in clinical trials. |
format | Online Article Text |
id | pubmed-3145341 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-31453412011-08-02 Prostate-Specific Membrane Antigen-Based Therapeutics Akhtar, Naveed H. Pail, Orrin Saran, Ankeeta Tyrell, Lauren Tagawa, Scott T. Adv Urol Review Article Prostate cancer (PC) is the most common noncutaneous malignancy affecting men in the US, leading to significant morbidity and mortality. While significant therapeutic advances have been made, available systemic therapeutic options are lacking. Prostate-specific membrane antigen (PSMA) is a highly-restricted prostate cell-surface antigen that may be targeted. While initial anti-PSMA monoclonal antibodies were suboptimal, the development of monoclonal antibodies such as J591 which are highly specific for the external domain of PSMA has allowed targeting of viable, intact prostate cancer cells. Radiolabeled J591 has demonstrated accurate and selective tumor targeting, safety, and efficacy. Ongoing studies using anti-PSMA radioimmunotherapy with (177)Lu-J591 seek to improve the therapeutic profile, select optimal candidates with biomarkers, combine with chemotherapy, and prevent or delay the onset of metastatic disease for men with biochemical relapse. Anti-PSMA monoclonal antibody-drug conjugates have also been developed with completed and ongoing early-phase clinical trials. As PSMA is a selective antigen that is highly overexpressed in prostate cancer, anti-PSMA-based immunotherapy has also been studied and utilized in clinical trials. Hindawi Publishing Corporation 2012 2011-07-17 /pmc/articles/PMC3145341/ /pubmed/21811498 http://dx.doi.org/10.1155/2012/973820 Text en Copyright © 2012 Naveed H. Akhtar et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Akhtar, Naveed H. Pail, Orrin Saran, Ankeeta Tyrell, Lauren Tagawa, Scott T. Prostate-Specific Membrane Antigen-Based Therapeutics |
title | Prostate-Specific Membrane Antigen-Based Therapeutics |
title_full | Prostate-Specific Membrane Antigen-Based Therapeutics |
title_fullStr | Prostate-Specific Membrane Antigen-Based Therapeutics |
title_full_unstemmed | Prostate-Specific Membrane Antigen-Based Therapeutics |
title_short | Prostate-Specific Membrane Antigen-Based Therapeutics |
title_sort | prostate-specific membrane antigen-based therapeutics |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3145341/ https://www.ncbi.nlm.nih.gov/pubmed/21811498 http://dx.doi.org/10.1155/2012/973820 |
work_keys_str_mv | AT akhtarnaveedh prostatespecificmembraneantigenbasedtherapeutics AT pailorrin prostatespecificmembraneantigenbasedtherapeutics AT saranankeeta prostatespecificmembraneantigenbasedtherapeutics AT tyrelllauren prostatespecificmembraneantigenbasedtherapeutics AT tagawascottt prostatespecificmembraneantigenbasedtherapeutics |