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Repeated PSMA-targeting radioligand therapy of metastatic prostate cancer with (131)I-MIP-1095
PURPOSE: Prostate-specific membrane antigen (PSMA)-targeting radioligand therapy (RLT) was introduced in 2011. The first report described the antitumor and side effects of a single dose. The aim of this analysis was to evaluate toxicity and antitumor activity after single and repetitive therapies. M...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5397661/ https://www.ncbi.nlm.nih.gov/pubmed/28280855 http://dx.doi.org/10.1007/s00259-017-3665-9 |
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author | Afshar-Oromieh, Ali Haberkorn, Uwe Zechmann, Christian Armor, Thomas Mier, Walter Spohn, Fabian Debus, Nils Holland-Letz, Tim Babich, John Kratochwil, Clemens |
author_facet | Afshar-Oromieh, Ali Haberkorn, Uwe Zechmann, Christian Armor, Thomas Mier, Walter Spohn, Fabian Debus, Nils Holland-Letz, Tim Babich, John Kratochwil, Clemens |
author_sort | Afshar-Oromieh, Ali |
collection | PubMed |
description | PURPOSE: Prostate-specific membrane antigen (PSMA)-targeting radioligand therapy (RLT) was introduced in 2011. The first report described the antitumor and side effects of a single dose. The aim of this analysis was to evaluate toxicity and antitumor activity after single and repetitive therapies. METHODS: Thirty-four men with metastatic castration-resistant prostate cancer received PSMA-RLT with (131)I-MIP-1095. Twenty-three patients received a second, and three patients a third dose, timed at PSA progression after an initial response to the preceding therapy. The applied doses were separated in three groups: <3.5, 3.5–5.0 and >5.0 GBq. Antitumor and side-effects were analyzed by blood samples and other clinical data. Follow-up was conducted for up to 5 years. RESULTS: The best therapeutic effect was achieved by the first therapy. A PSA decline of ≥50% was achieved in 70.6% of the patients. The second and third therapies were significantly less effective. There was neither an association between the applied activity and PSA response or the time-to-progression. Hematologic toxicities were less prevalent but presented in a higher percentage of patients with increasing number of therapies. After hematologic toxicities, xerostomia was the second most frequent side effect and presented more often and with higher intensity after the second or third therapy. CONCLUSION: The first dose of RLT with (131)I-MIP-1095 presented with low side effects and could significantly reduce the tumor burden in a majority of patients. The second and third therapies were less effective and presented with more frequent and more intense side effects, especially hematologic toxicities and xerostomia. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00259-017-3665-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5397661 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-53976612017-05-05 Repeated PSMA-targeting radioligand therapy of metastatic prostate cancer with (131)I-MIP-1095 Afshar-Oromieh, Ali Haberkorn, Uwe Zechmann, Christian Armor, Thomas Mier, Walter Spohn, Fabian Debus, Nils Holland-Letz, Tim Babich, John Kratochwil, Clemens Eur J Nucl Med Mol Imaging Original Article PURPOSE: Prostate-specific membrane antigen (PSMA)-targeting radioligand therapy (RLT) was introduced in 2011. The first report described the antitumor and side effects of a single dose. The aim of this analysis was to evaluate toxicity and antitumor activity after single and repetitive therapies. METHODS: Thirty-four men with metastatic castration-resistant prostate cancer received PSMA-RLT with (131)I-MIP-1095. Twenty-three patients received a second, and three patients a third dose, timed at PSA progression after an initial response to the preceding therapy. The applied doses were separated in three groups: <3.5, 3.5–5.0 and >5.0 GBq. Antitumor and side-effects were analyzed by blood samples and other clinical data. Follow-up was conducted for up to 5 years. RESULTS: The best therapeutic effect was achieved by the first therapy. A PSA decline of ≥50% was achieved in 70.6% of the patients. The second and third therapies were significantly less effective. There was neither an association between the applied activity and PSA response or the time-to-progression. Hematologic toxicities were less prevalent but presented in a higher percentage of patients with increasing number of therapies. After hematologic toxicities, xerostomia was the second most frequent side effect and presented more often and with higher intensity after the second or third therapy. CONCLUSION: The first dose of RLT with (131)I-MIP-1095 presented with low side effects and could significantly reduce the tumor burden in a majority of patients. The second and third therapies were less effective and presented with more frequent and more intense side effects, especially hematologic toxicities and xerostomia. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00259-017-3665-9) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2017-03-09 2017 /pmc/articles/PMC5397661/ /pubmed/28280855 http://dx.doi.org/10.1007/s00259-017-3665-9 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Afshar-Oromieh, Ali Haberkorn, Uwe Zechmann, Christian Armor, Thomas Mier, Walter Spohn, Fabian Debus, Nils Holland-Letz, Tim Babich, John Kratochwil, Clemens Repeated PSMA-targeting radioligand therapy of metastatic prostate cancer with (131)I-MIP-1095 |
title | Repeated PSMA-targeting radioligand therapy of metastatic prostate cancer with (131)I-MIP-1095 |
title_full | Repeated PSMA-targeting radioligand therapy of metastatic prostate cancer with (131)I-MIP-1095 |
title_fullStr | Repeated PSMA-targeting radioligand therapy of metastatic prostate cancer with (131)I-MIP-1095 |
title_full_unstemmed | Repeated PSMA-targeting radioligand therapy of metastatic prostate cancer with (131)I-MIP-1095 |
title_short | Repeated PSMA-targeting radioligand therapy of metastatic prostate cancer with (131)I-MIP-1095 |
title_sort | repeated psma-targeting radioligand therapy of metastatic prostate cancer with (131)i-mip-1095 |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5397661/ https://www.ncbi.nlm.nih.gov/pubmed/28280855 http://dx.doi.org/10.1007/s00259-017-3665-9 |
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