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Lutetium-177 Labelled PSMA Targeted Therapy in Advanced Prostate Cancer: Current Status and Future Perspectives
SIMPLE SUMMARY: For patients with advanced prostate cancer, many different treatment options are available. One option is the radioligand therapy with (177)Lutetium labelled prostate-specific membrane antigen (Lu-PSMA). This treatment showed good results in previous studies with only some non-severe...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8371469/ https://www.ncbi.nlm.nih.gov/pubmed/34359614 http://dx.doi.org/10.3390/cancers13153715 |
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author | Seitzer, Konstantin Egon Seifert, Robert Kessel, Katharina Roll, Wolfgang Schlack, Katrin Boegemann, Martin Rahbar, Kambiz |
author_facet | Seitzer, Konstantin Egon Seifert, Robert Kessel, Katharina Roll, Wolfgang Schlack, Katrin Boegemann, Martin Rahbar, Kambiz |
author_sort | Seitzer, Konstantin Egon |
collection | PubMed |
description | SIMPLE SUMMARY: For patients with advanced prostate cancer, many different treatment options are available. One option is the radioligand therapy with (177)Lutetium labelled prostate-specific membrane antigen (Lu-PSMA). This treatment showed good results in previous studies with only some non-severe side effects. This review offers a short overview about the application, current standings and the future perspective of the radioligand therapy with Lu-PSMA. An approval of this therapy is awaited within 2021. ABSTRACT: Patients suffering from metastatic castration-resistant prostate cancer (mCRPC) have a poor prognosis. As a further treatment option (177)Lutetium (Lu) prostate-specific membrane antigen (PSMA) radioligand therapy gained a significant interest of many investigators. Several publications showed great response and prolonged survival with limited adverse events. However, to this point, it still remains unclear which patients benefit the most from (177)Lu-PSMA therapy, and how to improve the treatment regimen to achieve best outcome while minimizing potential adverse events. The efficacy for mCRPC patients is a given fact, and with the newly published results of the VISION trial its approval is only a matter of time. Recently, investigators started to focus on treating prostate cancer patients in earlier disease stages and in combination with other compounds. This review gives a brief overview of the current state and the future perspectives of (177)Lu labelled PSMA radioligand therapy. |
format | Online Article Text |
id | pubmed-8371469 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83714692021-08-19 Lutetium-177 Labelled PSMA Targeted Therapy in Advanced Prostate Cancer: Current Status and Future Perspectives Seitzer, Konstantin Egon Seifert, Robert Kessel, Katharina Roll, Wolfgang Schlack, Katrin Boegemann, Martin Rahbar, Kambiz Cancers (Basel) Review SIMPLE SUMMARY: For patients with advanced prostate cancer, many different treatment options are available. One option is the radioligand therapy with (177)Lutetium labelled prostate-specific membrane antigen (Lu-PSMA). This treatment showed good results in previous studies with only some non-severe side effects. This review offers a short overview about the application, current standings and the future perspective of the radioligand therapy with Lu-PSMA. An approval of this therapy is awaited within 2021. ABSTRACT: Patients suffering from metastatic castration-resistant prostate cancer (mCRPC) have a poor prognosis. As a further treatment option (177)Lutetium (Lu) prostate-specific membrane antigen (PSMA) radioligand therapy gained a significant interest of many investigators. Several publications showed great response and prolonged survival with limited adverse events. However, to this point, it still remains unclear which patients benefit the most from (177)Lu-PSMA therapy, and how to improve the treatment regimen to achieve best outcome while minimizing potential adverse events. The efficacy for mCRPC patients is a given fact, and with the newly published results of the VISION trial its approval is only a matter of time. Recently, investigators started to focus on treating prostate cancer patients in earlier disease stages and in combination with other compounds. This review gives a brief overview of the current state and the future perspectives of (177)Lu labelled PSMA radioligand therapy. MDPI 2021-07-23 /pmc/articles/PMC8371469/ /pubmed/34359614 http://dx.doi.org/10.3390/cancers13153715 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Seitzer, Konstantin Egon Seifert, Robert Kessel, Katharina Roll, Wolfgang Schlack, Katrin Boegemann, Martin Rahbar, Kambiz Lutetium-177 Labelled PSMA Targeted Therapy in Advanced Prostate Cancer: Current Status and Future Perspectives |
title | Lutetium-177 Labelled PSMA Targeted Therapy in Advanced Prostate Cancer: Current Status and Future Perspectives |
title_full | Lutetium-177 Labelled PSMA Targeted Therapy in Advanced Prostate Cancer: Current Status and Future Perspectives |
title_fullStr | Lutetium-177 Labelled PSMA Targeted Therapy in Advanced Prostate Cancer: Current Status and Future Perspectives |
title_full_unstemmed | Lutetium-177 Labelled PSMA Targeted Therapy in Advanced Prostate Cancer: Current Status and Future Perspectives |
title_short | Lutetium-177 Labelled PSMA Targeted Therapy in Advanced Prostate Cancer: Current Status and Future Perspectives |
title_sort | lutetium-177 labelled psma targeted therapy in advanced prostate cancer: current status and future perspectives |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8371469/ https://www.ncbi.nlm.nih.gov/pubmed/34359614 http://dx.doi.org/10.3390/cancers13153715 |
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