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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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 |
work_keys_str_mv |
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1725689205868199936 |