<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Armstrong WR</submitter><funding>NCI NIH HHS</funding><pagination>1244-1251</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9364769</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>62(9)</volume><pubmed_abstract>The prostate-specific membrane antigen (PSMA) has been targeted for PET imaging and radioligand therapy (RLT) in patients with prostate cancer. Xerostomia is a common side effect of RLT because of the high salivary gland uptake of PSMA radioligands. Here, we aimed to determine the impact of monosodium glutamate (MSG) administration on PSMA-radioligand biodistribution within healthy organs and tumor lesions by using &lt;sup>68&lt;/sup>Ga-PSMA-11 PET imaging. &lt;b>Methods:&lt;/b> Sixteen men with prostate cancer were randomized (1:1) into oral ingestion and oral topical application ("swishing") arms. Each subject underwent 2 &lt;sup>68&lt;/sup>Ga-PSMA-11 PET/CT scans within 14 d under baseline and MSG conditions. The salivary glands and whole-body tumor lesions were segmented using qPSMA software. We quantified tracer uptake via SUV&lt;sub>mean&lt;/sub> and SUV&lt;sub>max&lt;/sub> and compared parameters within each patient. &lt;b>Results:&lt;/b> For the oral ingestion arm, salivary gland SUV&lt;sub>mean&lt;/sub> and SUV&lt;sub>max&lt;/sub> decreased on average from the control scan to the MSG scan by 45% ± 15% (&lt;i>P&lt;/i> = 0.004) and 53% ± 11% (&lt;i>P&lt;/i> &lt; 0.001), respectively. Tumor lesion SUV&lt;sub>mean&lt;/sub> and SUV&lt;sub>max&lt;/sub> also decreased by 38% (interquartile range, -67% to -33%) and -52% (interquartile range, -70% to -49%), respectively (&lt;i>P&lt;/i> = 0.018). Swishing had no significant effect on &lt;sup>68&lt;/sup>Ga-PSMA-11 accumulation in normal organs or tumor lesions. &lt;b>Conclusion:&lt;/b> Oral ingestion but not topical application of MSG reduced &lt;sup>68&lt;/sup>Ga-PSMA-11 uptake in salivary glands. Tumor uptake also declined; therefore, the clinical application of MSG is unlikely to be useful in the framework of RLT.</pubmed_abstract><journal>Journal of nuclear medicine : official publication, Society of Nuclear Medicine</journal><pubmed_title>The Impact of Monosodium Glutamate on &lt;sup>68&lt;/sup>Ga-PSMA-11 Biodistribution in Men with Prostate Cancer: A Prospective Randomized, Controlled Imaging Study.</pubmed_title><pmcid>PMC9364769</pmcid><funding_grant_id>P30 CA016042</funding_grant_id><funding_grant_id>P50 CA092131</funding_grant_id><pubmed_authors>Dahlbom M</pubmed_authors><pubmed_authors>Armstrong WR</pubmed_authors><pubmed_authors>Alano R</pubmed_authors><pubmed_authors>Thin P</pubmed_authors><pubmed_authors>Elashoff D</pubmed_authors><pubmed_authors>Nguyen K</pubmed_authors><pubmed_authors>Czernin J</pubmed_authors><pubmed_authors>Gardner L</pubmed_authors><pubmed_authors>Lira S</pubmed_authors><pubmed_authors>Gafita A</pubmed_authors><pubmed_authors>Grogan T</pubmed_authors><pubmed_authors>Calais J</pubmed_authors><pubmed_authors>Allen-Auerbach M</pubmed_authors><pubmed_authors>Zhu S</pubmed_authors><pubmed_authors>Booker K</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Impact of Monosodium Glutamate on &lt;sup>68&lt;/sup>Ga-PSMA-11 Biodistribution in Men with Prostate Cancer: A Prospective Randomized, Controlled Imaging Study.</name><description>The prostate-specific membrane antigen (PSMA) has been targeted for PET imaging and radioligand therapy (RLT) in patients with prostate cancer. Xerostomia is a common side effect of RLT because of the high salivary gland uptake of PSMA radioligands. Here, we aimed to determine the impact of monosodium glutamate (MSG) administration on PSMA-radioligand biodistribution within healthy organs and tumor lesions by using &lt;sup>68&lt;/sup>Ga-PSMA-11 PET imaging. &lt;b>Methods:&lt;/b> Sixteen men with prostate cancer were randomized (1:1) into oral ingestion and oral topical application ("swishing") arms. Each subject underwent 2 &lt;sup>68&lt;/sup>Ga-PSMA-11 PET/CT scans within 14 d under baseline and MSG conditions. The salivary glands and whole-body tumor lesions were segmented using qPSMA software. We quantified tracer uptake via SUV&lt;sub>mean&lt;/sub> and SUV&lt;sub>max&lt;/sub> and compared parameters within each patient. &lt;b>Results:&lt;/b> For the oral ingestion arm, salivary gland SUV&lt;sub>mean&lt;/sub> and SUV&lt;sub>max&lt;/sub> decreased on average from the control scan to the MSG scan by 45% ± 15% (&lt;i>P&lt;/i> = 0.004) and 53% ± 11% (&lt;i>P&lt;/i> &lt; 0.001), respectively. Tumor lesion SUV&lt;sub>mean&lt;/sub> and SUV&lt;sub>max&lt;/sub> also decreased by 38% (interquartile range, -67% to -33%) and -52% (interquartile range, -70% to -49%), respectively (&lt;i>P&lt;/i> = 0.018). Swishing had no significant effect on &lt;sup>68&lt;/sup>Ga-PSMA-11 accumulation in normal organs or tumor lesions. &lt;b>Conclusion:&lt;/b> Oral ingestion but not topical application of MSG reduced &lt;sup>68&lt;/sup>Ga-PSMA-11 uptake in salivary glands. Tumor uptake also declined; therefore, the clinical application of MSG is unlikely to be useful in the framework of RLT.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Sep</publication><modification>2024-11-08T14:32:54.524Z</modification><creation>2024-11-08T14:32:54.524Z</creation></dates><accession>S-EPMC9364769</accession><cross_references><pubmed>33509974</pubmed><doi>10.2967/jnumed.120.257931</doi></cross_references></HashMap>