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...

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Main Authors: Naveed H. Akhtar, Orrin Pail, Ankeeta Saran, Lauren Tyrell, Scott T. Tagawa
Format: Article
Language:English
Published: Hindawi Limited 2012-01-01
Series:Advances in Urology
Online Access:http://dx.doi.org/10.1155/2012/973820
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spelling doaj-1db5d7135eef40f58c92188a0cf35da92020-11-24T22:45:18ZengHindawi LimitedAdvances in Urology1687-63691687-63772012-01-01201210.1155/2012/973820973820Prostate-Specific Membrane Antigen-Based TherapeuticsNaveed H. Akhtar0Orrin Pail1Ankeeta Saran2Lauren Tyrell3Scott T. Tagawa4Division of Hematology and Medical Oncology, Weill Cornell Medical College, 525 E. 68th Street, Box 403, New York, NY 10065, USADivision of Hematology and Medical Oncology, Weill Cornell Medical College, 525 E. 68th Street, Box 403, New York, NY 10065, USADivision of Hematology and Medical Oncology, Weill Cornell Medical College, 525 E. 68th Street, Box 403, New York, NY 10065, USADivision of Hematology and Medical Oncology, Weill Cornell Medical College, 525 E. 68th Street, Box 403, New York, NY 10065, USADivision of Hematology and Medical Oncology, Weill Cornell Medical College, 525 E. 68th Street, Box 403, New York, NY 10065, USAProstate 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 177Lu-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.http://dx.doi.org/10.1155/2012/973820
collection DOAJ
language English
format Article
sources DOAJ
author Naveed H. Akhtar
Orrin Pail
Ankeeta Saran
Lauren Tyrell
Scott T. Tagawa
spellingShingle Naveed H. Akhtar
Orrin Pail
Ankeeta Saran
Lauren Tyrell
Scott T. Tagawa
Prostate-Specific Membrane Antigen-Based Therapeutics
Advances in Urology
author_facet Naveed H. Akhtar
Orrin Pail
Ankeeta Saran
Lauren Tyrell
Scott T. Tagawa
author_sort Naveed H. Akhtar
title Prostate-Specific Membrane Antigen-Based Therapeutics
title_short 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_sort prostate-specific membrane antigen-based therapeutics
publisher Hindawi Limited
series Advances in Urology
issn 1687-6369
1687-6377
publishDate 2012-01-01
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 177Lu-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.
url http://dx.doi.org/10.1155/2012/973820
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