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Muscarinic inhibition of salivary glands with glycopyrronium bromide does not reduce the uptake of PSMA-ligands or radioiodine
RATIONALE: Salivary glands are highly perfused and express the prostate-specific membrane antigen (PSMA) receptor as well as the sodium—iodide symporter. As a consequence, treatment with (177)Lu/(225)Ac-PSMA for prostate cancer or (131)I for thyroid cancer leads to a high radiation dose in the saliv...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7953192/ https://www.ncbi.nlm.nih.gov/pubmed/33710423 http://dx.doi.org/10.1186/s13550-021-00770-1 |
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author | Mohan, V. Bruin, N. M. Tesselaar, M. E. T. de Boer, J. P. Vegt, E. Hendrikx, J. J. M. A. Al-Mamgani, A. van de Kamer, J. B. Sonke, J.-J. Vogel, W. V. |
author_facet | Mohan, V. Bruin, N. M. Tesselaar, M. E. T. de Boer, J. P. Vegt, E. Hendrikx, J. J. M. A. Al-Mamgani, A. van de Kamer, J. B. Sonke, J.-J. Vogel, W. V. |
author_sort | Mohan, V. |
collection | PubMed |
description | RATIONALE: Salivary glands are highly perfused and express the prostate-specific membrane antigen (PSMA) receptor as well as the sodium—iodide symporter. As a consequence, treatment with (177)Lu/(225)Ac-PSMA for prostate cancer or (131)I for thyroid cancer leads to a high radiation dose in the salivary glands, and patients can be confronted with persistent xerostomia and reduced quality of life. Salivation can be inhibited using an antimuscarinic pharmaceutical, such as glycopyrronium bromide (GPB), which may also reduce perfusion. The primary objective of this work was to determine if inhibition with GPB could provide a considerable (> 30%) reduction in the accumulation of administered (123)I or (68)Ga-PSMA-11 in salivary glands. METHODS: Ten patients who already received a whole-body (68)Ga-PSMA-11 PET/CT scan for (re)staging of prostate cancer underwent a repeat PET/CT scan with tracer administration at 90 min after intravenous injection of 0.2 mg GPB. Four patients in follow-up after thyroid cancer, who had been treated with one round of ablative (131)I therapy with curative intent and had no signs of recurrence, received (123)I planar scintigraphy at 4 h after tracer administration without GPB and a repeated scan at least one week later, with tracer administration at 30 min after intramuscular injection of 0.4 mg GPB. Tracer uptake in the salivary glands was quantified on PET and scintigraphy, respectively, and values with and without GPB were compared. RESULTS: No significant difference in PSMA uptake in the salivary glands was seen without or with GPB (Mean SUL(mean) parotid glands control 5.57, intervention 5.72, p = 0.50. Mean SUL(mean) submandibular glands control 6.25, intervention 5.89, p = 0.12). Three out of 4 patients showed increased (123)I uptake in the salivary glands after GPB (Mean counts per pixel control 8.60, intervention 11.46). CONCLUSION: Muscarinic inhibition of salivation with GPB did not significantly reduce the uptake of PSMA-ligands or radioiodine in salivary glands, and can be dismissed as a potential strategy to reduce toxicity from radionuclide therapies. |
format | Online Article Text |
id | pubmed-7953192 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-79531922021-03-12 Muscarinic inhibition of salivary glands with glycopyrronium bromide does not reduce the uptake of PSMA-ligands or radioiodine Mohan, V. Bruin, N. M. Tesselaar, M. E. T. de Boer, J. P. Vegt, E. Hendrikx, J. J. M. A. Al-Mamgani, A. van de Kamer, J. B. Sonke, J.-J. Vogel, W. V. EJNMMI Res Original Research RATIONALE: Salivary glands are highly perfused and express the prostate-specific membrane antigen (PSMA) receptor as well as the sodium—iodide symporter. As a consequence, treatment with (177)Lu/(225)Ac-PSMA for prostate cancer or (131)I for thyroid cancer leads to a high radiation dose in the salivary glands, and patients can be confronted with persistent xerostomia and reduced quality of life. Salivation can be inhibited using an antimuscarinic pharmaceutical, such as glycopyrronium bromide (GPB), which may also reduce perfusion. The primary objective of this work was to determine if inhibition with GPB could provide a considerable (> 30%) reduction in the accumulation of administered (123)I or (68)Ga-PSMA-11 in salivary glands. METHODS: Ten patients who already received a whole-body (68)Ga-PSMA-11 PET/CT scan for (re)staging of prostate cancer underwent a repeat PET/CT scan with tracer administration at 90 min after intravenous injection of 0.2 mg GPB. Four patients in follow-up after thyroid cancer, who had been treated with one round of ablative (131)I therapy with curative intent and had no signs of recurrence, received (123)I planar scintigraphy at 4 h after tracer administration without GPB and a repeated scan at least one week later, with tracer administration at 30 min after intramuscular injection of 0.4 mg GPB. Tracer uptake in the salivary glands was quantified on PET and scintigraphy, respectively, and values with and without GPB were compared. RESULTS: No significant difference in PSMA uptake in the salivary glands was seen without or with GPB (Mean SUL(mean) parotid glands control 5.57, intervention 5.72, p = 0.50. Mean SUL(mean) submandibular glands control 6.25, intervention 5.89, p = 0.12). Three out of 4 patients showed increased (123)I uptake in the salivary glands after GPB (Mean counts per pixel control 8.60, intervention 11.46). CONCLUSION: Muscarinic inhibition of salivation with GPB did not significantly reduce the uptake of PSMA-ligands or radioiodine in salivary glands, and can be dismissed as a potential strategy to reduce toxicity from radionuclide therapies. Springer Berlin Heidelberg 2021-03-12 /pmc/articles/PMC7953192/ /pubmed/33710423 http://dx.doi.org/10.1186/s13550-021-00770-1 Text en © The Author(s) 2021 Open AccessThis 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/. |
spellingShingle | Original Research Mohan, V. Bruin, N. M. Tesselaar, M. E. T. de Boer, J. P. Vegt, E. Hendrikx, J. J. M. A. Al-Mamgani, A. van de Kamer, J. B. Sonke, J.-J. Vogel, W. V. Muscarinic inhibition of salivary glands with glycopyrronium bromide does not reduce the uptake of PSMA-ligands or radioiodine |
title | Muscarinic inhibition of salivary glands with glycopyrronium bromide does not reduce the uptake of PSMA-ligands or radioiodine |
title_full | Muscarinic inhibition of salivary glands with glycopyrronium bromide does not reduce the uptake of PSMA-ligands or radioiodine |
title_fullStr | Muscarinic inhibition of salivary glands with glycopyrronium bromide does not reduce the uptake of PSMA-ligands or radioiodine |
title_full_unstemmed | Muscarinic inhibition of salivary glands with glycopyrronium bromide does not reduce the uptake of PSMA-ligands or radioiodine |
title_short | Muscarinic inhibition of salivary glands with glycopyrronium bromide does not reduce the uptake of PSMA-ligands or radioiodine |
title_sort | muscarinic inhibition of salivary glands with glycopyrronium bromide does not reduce the uptake of psma-ligands or radioiodine |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7953192/ https://www.ncbi.nlm.nih.gov/pubmed/33710423 http://dx.doi.org/10.1186/s13550-021-00770-1 |
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