4.2 Review

Antibodies targeting Prostate-Specific Membrane Antigen positive prostate cancer: from diagnostic imaging to theranostics

Journal

CURRENT OPINION IN ONCOLOGY
Volume 33, Issue 5, Pages 500-506

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/CCO.0000000000000767

Keywords

antibody-drug conjugate; J591; prostate cancer; Prostate-Specific Membrane Antigen; radionuclide

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Targeting Prostate-Specific Membrane Antigen (PSMA) with antibodies has shown great promise in personalized medicine for prostate cancer patients, both for diagnostic and therapeutic purposes. Recent developments in PSMA-targeting antibodies have led to groundbreaking advances in PCa diagnosis and treatment, with the use of different radionuclides and drug conjugates showing potential in clinical trials. Despite safety concerns in some trials, PSMA has been validated as a crucial immunoconjugate target for further clinical investigation.
Purpose of review Targeting Prostate-Specific Membrane Antigen (PSMA) has paved the way for personalized medicine in prostate cancer (PCa) patients. This review aims to highlight the role of PSMA targeting antibodies in PCa, for diagnostic and therapeutic purposes. Recent findings PSMA Positron Emission Tomography/Computed Tomography has been a game changer in the diagnosis of PCa in the recent decade. Two anti-PSMA monoclonal antibodies have been studied in PCa: 7E11-C35 (limited use) and J591. J591 antibody was used for diagnostic purposes coupled with different radionuclides. Most importantly, it was combined to numerous therapeutic radionuclides such as Lutetium-177 (Lu-177), Yttrium-90 (Y-90), Indium-111 (In-111), and Actinium-225 (Ac-225). It was also conjugated to drugs forming antibody-drug conjugates (e.g. MLN2704 and PSMA-ADC). These compounds were tested in recent phase I/II clinical trials. PSMA targeting antibodies are very promising for further clinical investigation and continue to be a momentous research area, for both imaging and therapeutic settings. Although some clinical trials resulted in unfavorably safety profiles for some antibodies, they validated PSMA as a crucial immunoconjugate target.

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