Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/105473
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dc.contributor.authorZukotynski, K.-
dc.contributor.authorKim, C.-
dc.contributor.authorGerbaudo, V.-
dc.contributor.authorHainer, J.-
dc.contributor.authorTaplin, M.-E.-
dc.contributor.authorKantoff, P.-
dc.contributor.authorden Abbeele, A.-
dc.contributor.authorSeltzer, S.-
dc.contributor.authorSweeney, C.-
dc.date.issued2015-
dc.identifier.citationAmerican Journal of Nuclear Medicine and Molecular Imaging, 2015; 5(1):72-82-
dc.identifier.issn2160-8407-
dc.identifier.issn2160-8407-
dc.identifier.urihttp://hdl.handle.net/2440/105473-
dc.descriptionPMCID: PMC4299771-
dc.description.abstractTo evaluate (18)F-labeled-fluorodeoxyglucose ((18)F-FDG-) and (18)F-labeled-sodium fluoride ((18)F-NaF-) positron emission tomography/computed tomography (PET/CT) as biomarkers in metastatic castrate-resistant prostate cancer (mCRPC). Nine men (53-75 years) in a phase 1 trial of abiraterone and cabozantinib had (18)F-FDG-PET/CT, (18)F-NaF-PET/CT and standard imaging ((99m)Tc-labeled-methylene-diphosphonate ((99m)Tc-MDP) bone scan and abdominal/pelvic CT) at baseline and after 8 weeks of therapy. Baseline disease was classified as widespread (18)F-FDG-avid, oligometastatic (18)F-FDG-avid (1 site), or non-(18)F-FDG-avid. Metabolic response was classified using European Organisation for Research and Treatment of Cancer (EORTC) criteria. Treatment response using Response Evaluation Criteria in Solid Tumors (RECIST) 1.1, Prostate Cancer Working Group 2 (PCWG2) guidelines and days on trial (DOT) were recorded. All men were followed for 1 year or until progression. Four men had (18)F-FDG-avid disease: two with widespread (DOT 53 and 76) and two with oligometastatic disease (DOT 231 and still on trial after 742+ days). Five men had non-(18)F-FDG-avid disease; three remained stable or improved (2 still on trial while one discontinued for non-oncologic reasons; DOT 225-563+), and 2 progressed (DOT 285 and 532). Despite the small sample size, Kaplan-Meier analysis showed a significant difference in progression free survival (PFS) between men with widespread (18)F-FDG-avid, oligometastatic (18)F-FDG-avid and non-(18)F-FDG-avid disease (p < 0.01). All men had (18)F-NaF-avid disease. Neither (18)F-NaF-avid disease extent nor intensity was predictive of treatment response. (18)F-FDG-PET/CT may be superior to (18)F-NaF-PET/CT and standard imaging in men with mCRPC on abiraterone and cabozantinib. (18)F-FDG-PET/CT may have potential to stratify men into 3 groups (widespread vs. oligometastatic (18)F-FDG-avid vs. non-(18)F-FDG-avid mCRPC) to tailor therapy. Further evaluation is warranted.-
dc.description.statementofresponsibilityKatherine A Zukotynski, Chun K Kim, Victor H Gerbaudo, Jon Hainer, Mary-Ellen Taplin, Philip Kantoff, Annick D Van den Abbeele, Steven Seltzer, Christopher J Sweeney-
dc.language.isoen-
dc.publishere-Century Publishing Corporation-
dc.rightsAJNMMI Copyright © 2015-
dc.source.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4299771/-
dc.subjectFDG-
dc.subjectNaF-
dc.subjectPET/CT-
dc.subjectbone scan-
dc.subjectprostate cancer-
dc.title¹⁸F-FDG-PET/CT and ¹⁸F-NaF-PET/CT in men with castrate-resistant prostate cancer-
dc.title.alternative(18)F-FDG-PET/CT and (18)F-NaF-PET/CT in men with castrate-resistant prostate cancer-
dc.typeJournal article-
pubs.publication-statusPublished-
dc.identifier.orcidSweeney, C. [0000-0002-0398-6018]-
Appears in Collections:Aurora harvest 3
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