<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Makhlin I</submitter><funding>Susan G. Komen</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><pagination>e220032</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9713595</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>4(6)</volume><pubmed_abstract>Fluorine 18 (&lt;sup>18&lt;/sup>F) fluorodeoxyglucose (FDG) PET/CT has shown promise for use in assessing treatment response in patients with bone-only or bone-dominant (BD) metastatic breast cancer (mBC). In this single-institution, prospective single-arm study of 23 women (median age, 59 years [range, 38-81 years]) with biopsy-proven estrogen receptor-positive bone-only or BD mBC about to begin new endocrine therapy between October 3, 2013, and August 3, 2018, the value of early 4-week &lt;sup>18&lt;/sup>F-FDG PET/CT in predicting progression-free survival (PFS) was evaluated. &lt;sup>18&lt;/sup>F-FDG PET/CT was performed at baseline, 4 weeks, and 12 weeks. Maximum standardized uptake value (SUV&lt;sub>max&lt;/sub>) and peak SUV (SUV&lt;sub>peak&lt;/sub>) were measured for up to five index lesions. The primary end point was PFS. Secondary end points were overall survival (OS) and time to skeletal-related events (tSREs). All end points were compared between responders (reduction of 30% or more in the sum of SUV&lt;sub>max&lt;/sub> for target lesions) and nonresponders at 4 weeks and 12 weeks. Percentage change from baseline in SUV&lt;sub>max&lt;/sub> at 4- and 12-week &lt;sup>18&lt;/sup>F-FDG PET/CT were highly correlated (&lt;i>r&lt;/i> = 0.81). At the 4-week time point PET responders had numerically longer PFS (14.2 months vs 6.3 months; &lt;i>P&lt;/i> = .53), OS (44.0 months vs 29.7 months; &lt;i>P&lt;/i> = .47), and tSRE (27.4 months vs 25.2 months; &lt;i>P&lt;/i> = .66) compared with nonresponders, suggesting the clinical utility of 4-week &lt;sup>18&lt;/sup>F-FDG PET/CT as an early predictor of treatment failure. &lt;b>Keywords:&lt;/b> Breast Cancer, Metastatic Breast Cancer, Bone-Dominant Metastatic Breast Cancer, FDG PET/CT, Estrogen-Receptor Positive Metastatic Breast Cancer &lt;i>Supplemental material is available for this article.&lt;/i> Clinical trial registration no. NCT04316117 © RSNA, 2022.</pubmed_abstract><journal>Radiology. Imaging cancer</journal><pubmed_title>&lt;sup>18&lt;/sup>F-FDG PET/CT for the Evaluation of Therapy Response in Hormone Receptor-Positive Bone-Dominant Metastatic Breast Cancer.</pubmed_title><pmcid>PMC9713595</pmcid><funding_grant_id>T32 CA009615-30</funding_grant_id><funding_grant_id>T32 CA009615</funding_grant_id><pubmed_authors>Gillman J</pubmed_authors><pubmed_authors>Makhlin I</pubmed_authors><pubmed_authors>Pantel AR</pubmed_authors><pubmed_authors>Mankoff DA</pubmed_authors><pubmed_authors>Clark AS</pubmed_authors><pubmed_authors>Korhonen KE</pubmed_authors><pubmed_authors>Martin ML</pubmed_authors><pubmed_authors>Schubert E</pubmed_authors></additional><is_claimable>false</is_claimable><name>&lt;sup>18&lt;/sup>F-FDG PET/CT for the Evaluation of Therapy Response in Hormone Receptor-Positive Bone-Dominant Metastatic Breast Cancer.</name><description>Fluorine 18 (&lt;sup>18&lt;/sup>F) fluorodeoxyglucose (FDG) PET/CT has shown promise for use in assessing treatment response in patients with bone-only or bone-dominant (BD) metastatic breast cancer (mBC). In this single-institution, prospective single-arm study of 23 women (median age, 59 years [range, 38-81 years]) with biopsy-proven estrogen receptor-positive bone-only or BD mBC about to begin new endocrine therapy between October 3, 2013, and August 3, 2018, the value of early 4-week &lt;sup>18&lt;/sup>F-FDG PET/CT in predicting progression-free survival (PFS) was evaluated. &lt;sup>18&lt;/sup>F-FDG PET/CT was performed at baseline, 4 weeks, and 12 weeks. Maximum standardized uptake value (SUV&lt;sub>max&lt;/sub>) and peak SUV (SUV&lt;sub>peak&lt;/sub>) were measured for up to five index lesions. The primary end point was PFS. Secondary end points were overall survival (OS) and time to skeletal-related events (tSREs). All end points were compared between responders (reduction of 30% or more in the sum of SUV&lt;sub>max&lt;/sub> for target lesions) and nonresponders at 4 weeks and 12 weeks. Percentage change from baseline in SUV&lt;sub>max&lt;/sub> at 4- and 12-week &lt;sup>18&lt;/sup>F-FDG PET/CT were highly correlated (&lt;i>r&lt;/i> = 0.81). At the 4-week time point PET responders had numerically longer PFS (14.2 months vs 6.3 months; &lt;i>P&lt;/i> = .53), OS (44.0 months vs 29.7 months; &lt;i>P&lt;/i> = .47), and tSRE (27.4 months vs 25.2 months; &lt;i>P&lt;/i> = .66) compared with nonresponders, suggesting the clinical utility of 4-week &lt;sup>18&lt;/sup>F-FDG PET/CT as an early predictor of treatment failure. &lt;b>Keywords:&lt;/b> Breast Cancer, Metastatic Breast Cancer, Bone-Dominant Metastatic Breast Cancer, FDG PET/CT, Estrogen-Receptor Positive Metastatic Breast Cancer &lt;i>Supplemental material is available for this article.&lt;/i> Clinical trial registration no. NCT04316117 © RSNA, 2022.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-04T21:00:41.501Z</modification><creation>2025-04-04T21:00:41.501Z</creation></dates><accession>S-EPMC9713595</accession><cross_references><pubmed>36269154</pubmed><doi>10.1148/rycan.220032</doi></cross_references></HashMap>