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https://ahro.austin.org.au/austinjspui/handle/1/19812
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DC Field | Value | Language |
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dc.contributor.author | Emmett, Louise | - |
dc.contributor.author | Metser, Ur | - |
dc.contributor.author | Bauman, Glenn | - |
dc.contributor.author | Hicks, Rodney J | - |
dc.contributor.author | Weickhardt, Andrew | - |
dc.contributor.author | Davis, Ian D | - |
dc.contributor.author | Punwani, Shonit | - |
dc.contributor.author | Pond, Gregory R | - |
dc.contributor.author | Chua, Sue Siew-Chen | - |
dc.contributor.author | Ho, Bao | - |
dc.contributor.author | Johnston, Edward | - |
dc.contributor.author | Pouliot, Frederic | - |
dc.contributor.author | Scott, Andrew M | - |
dc.date | 2018-11-15 | - |
dc.date.accessioned | 2018-11-26T00:51:07Z | - |
dc.date.available | 2018-11-26T00:51:07Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | Journal of nuclear medicine : official publication, Society of Nuclear Medicine 2019; 60(6): 794-800 | - |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/19812 | - |
dc.description.abstract | Background: A significant proportion of men with rising PSA following radical prostatectomy (RP) fail prostate fossa salvage radiotherapy (SRT). This study assessed the ability of F18 fluoro-methyl-choline PET/CT(FCH), Ga-68 HBED-CC PSMA-11 PET/CT (PSMA) and pelvic multi-parametric magnetic resonance imaging (pelvic MRI) to identify men who will best benefit from SRT. Methods: Prospective, multisite, imaging study in men with rising PSA post RP, high-risk features (PSA > 0.2ng/mL and either Gleason Score (GS) > 7 or PSA doubling time <10 months, or PSA >1.0ng/mL) and negative /equivocal conventional imaging (CT and bone scan) being considered for SRT. FCH (91/91), Pelvic MRI (88/91) and PSMA (31/91) (Australia only) were performed within two weeks. Imaging was interpreted by experienced local and central reads blinded to other imaging results with consensus for discordance. Imaging results were validated using a composite reference standard. Expected management was documented pre and post- imaging, and all treatments, biopsies and PSA collected for 3 years. Treatment response to SRT was defined as > 50% PSA reduction without androgen deprivation therapy. Results: Median GS, PSA at imaging and PSA doubling time were 8, 0.42(IQR 0.29-0.93) ng/mL, and 5.0 (IQR 3.3-7.6) months, respectively. Overall recurrent PCa was detected in 28% (25/88) with pelvic MRI, 32% (29/91) FCH and 42% (13/31) PSMA. This was within the prostate fossa (PF) in 21.5% (19/88), 13% (12/91) and 19% (6/31), with extra PF sites in 8% (7/88), 19% (17/91), and 32% (10/31) for MRI, FCH and PSMA (< 0.004). 94% (16/17) extra- PF sites on FCH were within the field of view of pelvic MRI. The detection rate for intrapelvic extra-PF disease was 90% (9/10) for PSMA and 31% (5/16) for MRI compared to FCH. Imaging changed expected management in 46% (42/91) FCH, and 23% (21/88) MRI. PSMA provided additive management change over FCH in a further 23% (7/31). Treatment response to SRT was higher in men with negative or PF confined vs. extra PF disease. FCH 73% (32/44) vs. 33% (3/9) (p< 0.02), pelvic MRI 70% (32/46) vs 50% (2/4), P = ns) and PSMA 88% (7/8) vs. 14% (1/7) (p<0.005). Men with negative imging (MRI, FCH +/- PSMA) had high (78%) response rates to SRT. Conclusion: FCH and PSMA had high detection rates for extra PF disease in men with negative/equivocal conventional imaging and BCR post RP. This impacted management and treatment responses to SRT, suggesting an important role for PET in triaging men being considered for curative SRT. | - |
dc.language.iso | eng | - |
dc.subject | Fluoromethyl-choline | - |
dc.subject | MRI | - |
dc.subject | Molecular Imaging | - |
dc.subject | Oncology: GU | - |
dc.subject | PET | - |
dc.subject | PSMA | - |
dc.subject | Prostate cancer | - |
dc.subject | biochemical recurrence | - |
dc.title | A Prospective, Multi-site, International Comparison of F-18 fluoro-methyl-choline, multi-parametric magnetic resonance and Ga-68 HBED-CC (PSMA-11) in men with High-Risk Features and Biochemical Failure after Radical Prostatectomy: Clinical Performance and Patient Outcomes. | - |
dc.type | Journal Article | - |
dc.identifier.journaltitle | Journal of nuclear medicine : official publication, Society of Nuclear Medicine | - |
dc.identifier.affiliation | Université Laval, Canada | en |
dc.identifier.affiliation | University College London, United Kingdom | en |
dc.identifier.affiliation | Eastern Health, Australia | en |
dc.identifier.affiliation | Monash University and Eastern Health, Australia | en |
dc.identifier.affiliation | St Vincent's Hospital, Australia | en |
dc.identifier.affiliation | Austin Health, Heidelberg, Victoria, Australia | en |
dc.identifier.affiliation | University of Toronto, Canada | en |
dc.identifier.affiliation | McMaster University, Canada | en |
dc.identifier.affiliation | St Vincent's Hospital, Sydney, Australia | en |
dc.identifier.affiliation | Peter MacCallum Cancer Institute, Australia | en |
dc.identifier.affiliation | London Health Sciences Center, United Kingdom | - |
dc.identifier.affiliation | The Royal Marsden Hospital NHS Foundation Trust, United Kingdom | - |
dc.identifier.affiliation | University College, United Kingdom | - |
dc.identifier.doi | 10.2967/jnumed.118.220103 | - |
dc.identifier.orcid | 0000-0002-6656-295X | - |
dc.identifier.pubmedid | 30442757 | - |
dc.type.austin | Journal Article | - |
local.name.researcher | Scott, Andrew M | |
item.languageiso639-1 | en | - |
item.cerifentitytype | Publications | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.grantfulltext | none | - |
item.openairetype | Journal Article | - |
item.fulltext | No Fulltext | - |
crisitem.author.dept | Molecular Imaging and Therapy | - |
crisitem.author.dept | Olivia Newton-John Cancer Research Institute | - |
Appears in Collections: | Journal articles |
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