Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/11514
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dc.contributor.authorLee, Sze Tingen
dc.contributor.authorLawrentschuk, Nathanen
dc.contributor.authorScott, Andrew Men
dc.date.accessioned2015-05-16T01:07:40Z
dc.date.available2015-05-16T01:07:40Z
dc.date.issued2012-07-01en
dc.identifier.citationSeminars in Nuclear Medicine; 42(4): 231-46en
dc.identifier.govdoc22681672en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/11514en
dc.description.abstract(18)F-fluorodeoxyglucose (FDG) is the most common positron emission tomography (PET) radiotracer used in prostate and bladder cancer evaluation, but its role is hampered by a generally low glucose metabolic rate in primary prostate carcinoma, and physiological excretion of FDG through the urinary system masking FDG uptake in primary bladder and prostate carcinoma. FDG-PET may have a role in selected patients for staging and restaging advanced prostate cancer, particularly in patients with an increasing prostatic-specific antigen (PSA) level. The use of diuresis strategies facilitates the identification of primary bladder cancer, and may be useful in staging extravesical spread of disease. FDG-PET may also be useful in patients with ureteric and urethral cancers. New PET tracers are showing promise in the staging and biological characterization of prostate cancer, which can assist with therapeutic decision making in patients undergoing radiotherapy of primary disease, and in the assessment of metastatic disease.en
dc.language.isoenen
dc.subject.otherHumansen
dc.subject.otherMaleen
dc.subject.otherNeoplasm Metastasisen
dc.subject.otherNeoplasm Stagingen
dc.subject.otherPositron-Emission Tomography.methodsen
dc.subject.otherProstatic Neoplasms.pathology.radionuclide imagingen
dc.subject.otherUrinary Bladder Neoplasms.pathology.radionuclide imagingen
dc.titlePET in prostate and bladder tumors.en
dc.typeJournal Articleen
dc.identifier.journaltitleSeminars in nuclear medicineen
dc.identifier.affiliationCentre for PET, Austin Hospital, Melbourne, Australiaen
dc.identifier.doi10.1053/j.semnuclmed.2012.03.002en
dc.description.pages231-46en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/22681672en
dc.type.austinJournal Articleen
local.name.researcherLee, Sze Ting
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
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