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(177)Lu-PSMA Therapy in Metastatic Castration-Resistant Prostate Cancer
The aim of this narrative review is to evaluate the current status of (177)Lu-PSMA (prostate specific membrane antigen) therapy for metastatic castration-resistant prostate cancer (mCRPC) in the light of the current literature. We also addressed patient preparation, therapy administration and side e...
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/PMC8071500/ https://www.ncbi.nlm.nih.gov/pubmed/33921146 http://dx.doi.org/10.3390/biomedicines9040430 |
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author | Sanli, Yasemin Simsek, Duygu Has Sanli, Oner Subramaniam, Rathan M. Kendi, Ayse Tuba |
author_facet | Sanli, Yasemin Simsek, Duygu Has Sanli, Oner Subramaniam, Rathan M. Kendi, Ayse Tuba |
author_sort | Sanli, Yasemin |
collection | PubMed |
description | The aim of this narrative review is to evaluate the current status of (177)Lu-PSMA (prostate specific membrane antigen) therapy for metastatic castration-resistant prostate cancer (mCRPC) in the light of the current literature. We also addressed patient preparation, therapy administration and side effect profiles. (177)Lu-PSMA therapy efficacy was assessed by using prospective trials, meta-analyses and major retrospective trials. Predictors of efficacy were also mentioned. Although there are some different approaches regarding the use of (177)Lu-PSMA therapy in different countries, this type of therapy is generally safe, with a low toxicity profile. From the oncological point of view, a PSA (prostate specific antigen) decline of ≥50% was seen in 10.6–69% of patients with mCRPC; whereas progression-free survival (PFS) was reported to be 3–13.7 months in different studies. Consequently, (177)Lu-PSMA therapy is a promising treatment in patients with mCRPC, with good clinical efficacy, even in heavily pretreated patients with multiple lines of systemic therapy. Currently, there are ongoing clinical trials in the United States, including a phase III multicenter FDA registration trial. |
format | Online Article Text |
id | pubmed-8071500 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80715002021-04-26 (177)Lu-PSMA Therapy in Metastatic Castration-Resistant Prostate Cancer Sanli, Yasemin Simsek, Duygu Has Sanli, Oner Subramaniam, Rathan M. Kendi, Ayse Tuba Biomedicines Review The aim of this narrative review is to evaluate the current status of (177)Lu-PSMA (prostate specific membrane antigen) therapy for metastatic castration-resistant prostate cancer (mCRPC) in the light of the current literature. We also addressed patient preparation, therapy administration and side effect profiles. (177)Lu-PSMA therapy efficacy was assessed by using prospective trials, meta-analyses and major retrospective trials. Predictors of efficacy were also mentioned. Although there are some different approaches regarding the use of (177)Lu-PSMA therapy in different countries, this type of therapy is generally safe, with a low toxicity profile. From the oncological point of view, a PSA (prostate specific antigen) decline of ≥50% was seen in 10.6–69% of patients with mCRPC; whereas progression-free survival (PFS) was reported to be 3–13.7 months in different studies. Consequently, (177)Lu-PSMA therapy is a promising treatment in patients with mCRPC, with good clinical efficacy, even in heavily pretreated patients with multiple lines of systemic therapy. Currently, there are ongoing clinical trials in the United States, including a phase III multicenter FDA registration trial. MDPI 2021-04-15 /pmc/articles/PMC8071500/ /pubmed/33921146 http://dx.doi.org/10.3390/biomedicines9040430 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 Sanli, Yasemin Simsek, Duygu Has Sanli, Oner Subramaniam, Rathan M. Kendi, Ayse Tuba (177)Lu-PSMA Therapy in Metastatic Castration-Resistant Prostate Cancer |
title | (177)Lu-PSMA Therapy in Metastatic Castration-Resistant Prostate Cancer |
title_full | (177)Lu-PSMA Therapy in Metastatic Castration-Resistant Prostate Cancer |
title_fullStr | (177)Lu-PSMA Therapy in Metastatic Castration-Resistant Prostate Cancer |
title_full_unstemmed | (177)Lu-PSMA Therapy in Metastatic Castration-Resistant Prostate Cancer |
title_short | (177)Lu-PSMA Therapy in Metastatic Castration-Resistant Prostate Cancer |
title_sort | (177)lu-psma therapy in metastatic castration-resistant prostate cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8071500/ https://www.ncbi.nlm.nih.gov/pubmed/33921146 http://dx.doi.org/10.3390/biomedicines9040430 |
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