Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/21542
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dc.contributor.authorVargas, Hebert Alberto-
dc.contributor.authorKramer, Gem M-
dc.contributor.authorScott, Andrew M-
dc.contributor.authorWeickhardt, Andrew-
dc.contributor.authorMeier, Andreas A-
dc.contributor.authorParada, Nicole-
dc.contributor.authorBeattie, Bradley J-
dc.contributor.authorHumm, John L-
dc.contributor.authorStaton, Kevin D-
dc.contributor.authorZanzonico, Pat B-
dc.contributor.authorLyashchenko, Serge K-
dc.contributor.authorLewis, Jason S-
dc.contributor.authorYaqub, Maqsood-
dc.contributor.authorSosa, Ramon E-
dc.contributor.authorvan den Eertwegh, Alfons J-
dc.contributor.authorDavis, Ian D-
dc.contributor.authorAckermann, Uwe-
dc.contributor.authorPathmaraj, Kunthi-
dc.contributor.authorSchuit, Robert C-
dc.contributor.authorWindhorst, Albert D-
dc.contributor.authorChua, Sue-
dc.contributor.authorWeber, Wolfgang A-
dc.contributor.authorLarson, Steven M-
dc.contributor.authorScher, Howard I-
dc.contributor.authorLammertsma, Adriaan A-
dc.contributor.authorHoekstra, Otto S-
dc.contributor.authorMorris, Michael J-
dc.date2018-04-06-
dc.date.accessioned2019-08-12T05:01:13Z-
dc.date.available2019-08-12T05:01:13Z-
dc.date.issued2018-10-
dc.identifier.citationJournal of Nuclear Medicine 2018; 59(10): 1516-1523-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/21542-
dc.description.abstract18F-fluorodihydrotestosterone (18F-FDHT) is a radiolabeled analog of the androgen receptor's primary ligand that is currently being credentialed as a biomarker for prognosis, response, and pharmacodynamic effects of new therapeutics. As part of the biomarker qualification process, we prospectively assessed its reproducibility and repeatability in men with metastatic castration-resistant prostate cancer. Methods: We conducted a prospective multiinstitutional study of metastatic castration-resistant prostate cancer patients undergoing 2 (test/retest) 18F-FDHT PET/CT scans on 2 consecutive days. Two independent readers evaluated all examinations and recorded SUVs, androgen receptor-positive tumor volumes, and total lesion uptake for the most avid lesion detected in each of 32 predefined anatomic regions. The relative absolute difference and reproducibility coefficient (RC) of each metric were calculated between the test and retest scans. Linear regression analyses, intraclass correlation coefficients (ICCs), and Bland-Altman plots were used to evaluate repeatability of 18F-FDHT metrics. The coefficient of variation and ICC were used to assess interobserver reproducibility. Results: Twenty-seven patients with 140 18F-FDHT-avid regions were included. The best repeatability among 18F-FDHT uptake metrics was found for SUV metrics (SUVmax, SUVmean, and SUVpeak), with no significant differences in repeatability among them. Correlations between the test and retest scans were strong for all SUV metrics (R2 ≥ 0.92; ICC ≥ 0.97). The RCs of the SUV metrics ranged from 21.3% (SUVpeak) to 24.6% (SUVmax). The test and retest androgen receptor-positive tumor volumes and TLU, respectively, were highly correlated (R2 and ICC ≥ 0.97), although variability was significantly higher than that for SUV (RCs > 46.4%). The prostate-specific antigen levels, Gleason score, weight, and age did not affect repeatability, nor did total injected activity, uptake measurement time, or differences in uptake time between the 2 scans. Including the most avid lesion per patient, the 5 most avid lesions per patient, only lesions 4.2 mL or more, only lesions with an SUV of 4 g/mL or more, or normalizing of SUV to area under the parent plasma activity concentration-time curve did not significantly affect repeatability. All metrics showed high interobserver reproducibility (ICC > 0.98; coefficient of variation < 0.2%-10.8%). Conclusion: Uptake metrics derived from 18F-FDHT PET/CT show high repeatability and interobserver reproducibility.-
dc.language.isoeng-
dc.subjectFDHT-
dc.subjectPET-
dc.subjectProstate cancer-
dc.subjectrepeatability-
dc.subjectreproducibility-
dc.titleReproducibility and Repeatability of Semiquantitative 18F-Fluorodihydrotestosterone Uptake Metrics in Castration-Resistant Prostate Cancer Metastases: A Prospective Multicenter Study.-
dc.typeJournal Article-
dc.identifier.journaltitleJournal of Nuclear Medicine-
dc.identifier.affiliationDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.-
dc.identifier.affiliationDepartment of Nuclear Medicine, Royal Marsden NHS Foundation Trust, Sutton, United Kingdomen
dc.identifier.affiliationDepartment of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, New York, USAen
dc.identifier.affiliationDepartment of Radiology, Weill Cornell Medicine, New York, New York, USAen
dc.identifier.affiliationDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York, USAen
dc.identifier.affiliationDepartment of Medicine, Weill Cornell Medicine, New York, New York, USAen
dc.identifier.affiliationDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USAen
dc.identifier.affiliationDepartment of Medical Oncology, VU University Medical Centre, Amsterdam, The Netherlandsen
dc.identifier.affiliationMonash University and Eastern Health, Eastern Health Clinical School, Box Hill, Australiaen
dc.identifier.affiliationDepartment of Nuclear Medicine and Centre for PET, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationDepartment of Radiology and Nuclear Medicine, VU University Medical Centre, Amsterdam, The Netherlandsen
dc.identifier.affiliationDepartment of Medicine, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationOlivia Newton-John Cancer Research Institute, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationLa Trobe University, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationDepartment of Molecular Imaging and Therapy, The University of Melbourne, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationDepartment of Medical Oncology, Olivia Newton-John Cancer Wellness and Research Centre, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.doi10.2967/jnumed.117.206490-
dc.identifier.orcid0000-0002-6656-295X-
dc.identifier.pubmedid29626121-
dc.type.austinClinical Trial-
dc.type.austinJournal Article-
dc.type.austinMulticenter Study-
dc.type.austinResearch Support, Non-U.S. Gov't-
local.name.researcherAckermann, Uwe
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptMolecular Imaging and Therapy-
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