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Theragnostics in prostate cancer. | LitMetric

Theragnostics in prostate cancer.

Q J Nucl Med Mol Imaging

Division of Nuclear Medicine, IRCCS University Hospital of Bologna, Bologna, Italy.

Published: December 2021

AI Article Synopsis

  • - Prostate-specific membrane antigen (PSMA) is a key target for both diagnosing and treating prostate cancer, supporting a personalized medicine approach known as theragnostics.
  • - Recent FDA approvals of PSMA PET imaging drugs and promising results from studies like the VISION trial highlight PSMA's growing importance in oncology and its effectiveness in treating aggressive prostate cancer.
  • - This review aims to summarize recent advancements in prostate cancer theragnostics, emphasizing current clinical uses and future possibilities in treatment.

Article Abstract

Prostate-specific membrane antigen (PSMA) is a molecular target for both imaging diagnostics and therapeutics, i.e., a theragnostics target. There has been a growing body of evidence supporting PSMA theragnostics approaches in the management of prostate cancer (PCa) for tailored precision medicine. Tumor characterization through PSMA-ligand PET imaging is crucial for assessing the molecular signature and eligibility for PSMA radioligand therapy. Recent U.S. Food and Drug Administration (FDA) approval of two new drug applications for PSMA PET imaging contribute to reinforce PSMA as an oncologic blockbuster. Additionally, relevant progress in the PSMA treatment has been made in the last five years. [Lu]Lu-PSMA-617 radioligand therapy for patients with progressive PSMA-avid metastatic castration-resistant PCa (mCRPC) significantly increased overall survival and radiographic progression-free survival, according to the results of an international, prospective, open label, multicenter, randomized, phase III study (VISION trial). The objective of this comprehensive review is to highlight the recent advances in PCa theragnostics, focusing on actual clinical applications and future perspectives.

Download full-text PDF

Source
http://dx.doi.org/10.23736/S1824-4785.21.03419-1DOI Listing

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