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      Towards Improving the Efficacy of PSMA-Targeting Radionuclide Therapy for Late-Stage Prostate Cancer—Combination Strategies

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          Abstract

          Purpose of Review

          [ 177Lu]Lu-PSMA-617 is a radiopharmaceutical that emits beta-minus radiation and targets prostate-specific membrane antigen (PSMA)-positive prostate cancer. Despite its clinical success, there are still patients not showing sufficient response rates. This review compiles latest studies aiming at therapy improvement in [ 177Lu]Lu-PSMA-617-naïve and -resistant patients by alternative or combination treatments.

          Recent Findings

          A variety of agents to combine with [ 177Lu]Lu-PSMA-617 are currently under investigation including alpha radiation-emitting pharmaceuticals, radiosensitizers, taxane chemotherapeutics, androgen receptor pathway inhibitors, immune checkpoint inhibitors, and external beam radiation. Actinium-225 ( 225Ac)-labeled PSMA-targeting inhibitors are the most studied pharmaceuticals for combination therapy or as an alternative for treatment after progression under [ 177Lu]Lu-PSMA-617 therapy.

          Summary

          Alpha emitters seem to have a potential of achieving a response to PSMA-targeting radionuclide therapy in both initial non-responders or responders to [ 177Lu]Lu-PSMA-617 later developing treatment resistance. Emerging evidence for immunostimulatory effects of radiopharmaceuticals and first prospective studies support the combination of [ 177Lu]Lu-PSMA-617 and immune checkpoint inhibition for late-stage prostate cancer.

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          Most cited references35

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          Lutetium-177–PSMA-617 for Metastatic Castration-Resistant Prostate Cancer

          Metastatic castration-resistant prostate cancer remains fatal despite recent advances. Prostate-specific membrane antigen (PSMA) is highly expressed in metastatic castration-resistant prostate cancer. Lutetium-177 (177Lu)-PSMA-617 is a radioligand therapy that delivers beta-particle radiation to PSMA-expressing cells and the surrounding microenvironment.
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            [177Lu]Lu-PSMA-617 versus cabazitaxel in patients with metastatic castration-resistant prostate cancer (TheraP): a randomised, open-label, phase 2 trial

            Lutetium-177 [177Lu]Lu-PSMA-617 is a radiolabelled small molecule that delivers β radiation to cells expressing prostate-specific membrane antigen (PSMA), with activity and safety in patients with metastatic castration-resistant prostate cancer. We aimed to compare [177Lu]Lu-PSMA-617 with cabazitaxel in patients with metastatic castration-resistant prostate cancer.
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              German Multicenter Study Investigating 177Lu-PSMA-617 Radioligand Therapy in Advanced Prostate Cancer Patients.

              (177)Lu-labeled PSMA-617 is a promising new therapeutic agent for radioligand therapy (RLT) of patients with metastatic castration-resistant prostate cancer (mCRPC). Initiated by the German Society of Nuclear Medicine, a retrospective multicenter data analysis was started in 2015 to evaluate efficacy and safety of (177)Lu-PSMA-617 in a large cohort of patients.
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                Author and article information

                Contributors
                matthias.eder@uniklinik-freiburg.de
                Journal
                Curr Oncol Rep
                Curr Oncol Rep
                Current Oncology Reports
                Springer US (New York )
                1523-3790
                1534-6269
                20 October 2023
                20 October 2023
                2023
                : 25
                : 11
                : 1363-1374
                Affiliations
                [1 ]GRID grid.5963.9, Department of Nuclear Medicine, University Medical Center Freiburg, Faculty of Medicine, , University of Freiburg, ; Hugstetter Str. 55, 79106 Freiburg, Germany
                [2 ]GRID grid.7497.d, ISNI 0000 0004 0492 0584, Division of Radiopharmaceutical Development, German Cancer Consortium (DKTK), Partner Site Freiburg, Freiburg, , Germany and German Cancer Research Center, ; Heidelberg, Germany
                [3 ]GRID grid.5963.9, Department of Radiation Oncology, University Medical Center Freiburg, Faculty of Medicine, , University of Freiburg, ; Freiburg, Germany
                [4 ]GRID grid.5963.9, Department of Urology, University Medical Center Freiburg, Faculty of Medicine, , University of Freiburg, ; Freiburg, Germany
                Author information
                http://orcid.org/0000-0002-5110-0744
                Article
                1458
                10.1007/s11912-023-01458-6
                10640479
                37861915
                c846655d-4cdc-42c6-b984-3b42b6941487
                © The Author(s) 2023

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 4 September 2023
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001659, Deutsche Forschungsgemeinschaft;
                Award ID: BA 6696/2-1
                Award Recipient :
                Funded by: Deutsches Krebsforschungszentrum (DKFZ) (1052)
                Categories
                Article
                Custom metadata
                © Springer Science+Business Media, LLC, part of Springer Nature 2023

                Oncology & Radiotherapy
                metastatic castration-resistant prostate cancer,lutetium-177-psma-617,radioligand therapy,combination therapy,prostate-specific membrane antigen

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