Abstract

Simple SummaryThe prognosis for metastatic prostate cancer patients remains poor. Prostate-specific membrane antigen (PSMA) is overexpressed in prostate cancer and is a promising target for both imaging and therapy. In this review paper, we provide an overview of the evidence for PSMA-targeted imaging in prostate cancer, focusing on different imaging modalities and their theranostic applications. We will also review PSMA-targeted radioligand therapy, focusing on lutetium-177 radioligand therapy and alpha-emitting radioligand therapy with actinium-225. Combination regimens with lutetium-177 and other systemic therapy agents will be reviewed. Antibody-based radioimmunotherapy will also be discussed along with other noteworthy radionuclide agents.Introduction: Prostate-specific membrane antigen (PSMA) is a promising novel molecular target for imaging diagnostics and therapeutics (theranostics). There has been a growing body of evidence supporting PSMA theranostics approaches in optimizing the management of prostate cancer and potentially altering its natural history. Methods: We utilized PubMed and Google Scholar for published studies, and clinicaltrials.gov for planned, ongoing, and completed clinical trials in PSMA theranostics as of June 2021. We presented evolving evidence for various PSMA-targeted radiopharmaceutical agents in the treatment paradigm for prostate cancer, as well as combination treatment strategies with other targeted therapy and immunotherapy. We highlighted the emerging evidence of PSMA and fluorodeoxyglucose (FDG) PET/CT as a predictive biomarker for PSMA radioligand therapy. We identified seven ongoing clinical trials in oligometastatic-directed therapy using PSMA PET imaging. We also presented a schematic overview of 17 key PSMA theranostic clinical trials throughout the various stages of prostate cancer. Conclusions: In this review, we presented the contemporary and future landscape of theranostic applications in prostate cancer with a focus on PSMA ligands. As PSMA theranostics will soon become the standard of care for the management of prostate cancer, we underscore the importance of integrating nuclear medicine physicians into the multidisciplinary team.

Highlights

  • Prostate-specific membrane antigen (PSMA) is a promising novel molecular target for imaging diagnostics and therapeutics

  • According to consensus statements on PSMA positron emission tomography (PET)/CT response assessment criteria, from a panel of international experts recruited by European Association of Nuclear Medicine (EANM) and EAU (European Association of Urology), PSMA PET/CT should not be performed to assess response within three months after initiation of systemic therapy in hormone sensitive prostate cancer

  • According to consensus statements on PSMA PET/CT response assessment criteria, from a panel of international experts recruited by European Association of Nuclear Medicine (EANM) and EAU (European Association of Urology), PSMA PET/CT should not be performed to assess response within three months after initiation of systemic therap4yofi1n7 hormone sensitive prostate cancer

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Summary

Introduction

Prostate cancer represents a significant public health problem in the world. It is the second most common cancer and fifth leading cause of cancer death among men in 2020 [1]. The level of expression may increase with tumor dedifferentiation and castration resistance, neuroendocrine prostate cancer may have a decreased level of PSMA [4]. Even though this antigen is not entirely specific to prostate cancer cells, it can serve as a target for imaging and therapy due to its tumoral overexpression with relatively low toxicity to healthy tissues showing uptake [5]. Cautions need to be taken when interpreting 18F-PSMA-1007 PET scans, as there have been reports of focal unspecific bone uptake, defined as focal mild-to-moderate uptake (SUVmax < 10.0) not obviously related to a benign or malignant cause [12]

Clinical Applications of PSMA-Targeted Imaging
Biomarker for Evaluating Treatment Response
PSMA-Targeted Radioligand Therapy
Combination of 177Lu-PSMA-617 with ARATs
Combination of 177Lu-PSMA-617 with DNA Damage Repair Inhibitors
Combination of 177Lu-PSMA-617 with Immune Checkpoint Inhibitors
Other Notable Beta-Emitting PSMA-Targeted Radionuclide Therapy Agents
Findings
Conclusions
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