Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/20838
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dc.contributor.authorVan Binnebeek, S.-
dc.contributor.authorVanbilloen, B.-
dc.contributor.authorBaete, K.-
dc.contributor.authorTerwinghe, C.-
dc.contributor.authorKoole, M.-
dc.contributor.authorMottaghy, F. M.-
dc.contributor.authorClement, P. M.-
dc.contributor.authorMortelmans, L.-
dc.contributor.authorBOGAERTS, Kris-
dc.contributor.authorHaustermans, K.-
dc.contributor.authorNackaerts, K.-
dc.contributor.authorVan Cutsem, E.-
dc.contributor.authorVerslype, C.-
dc.contributor.authorVerbruggen, A.-
dc.contributor.authorDeroose, C.-
dc.date.accessioned2016-03-30T13:37:07Z-
dc.date.available2016-03-30T13:37:07Z-
dc.date.issued2016-
dc.identifier.citationEUROPEAN RADIOLOGY, 26(3), p. 900-909-
dc.identifier.issn0938-7994-
dc.identifier.urihttp://hdl.handle.net/1942/20838-
dc.description.abstractObjectives To compare the diagnostic accuracy of 111Inpentetreotide-scintigraphy with 68Ga-DOTATOC-positron emission tomography (PET)/computed tomography (CT) in patients with metastatic-neuroendocrine tumour (NET) scheduled for peptide receptor radionuclide therapy (PRRT). Incremental lesions (ILs) were defined as lesions observed on only one modality. Methods Fifty-three metastatic-NET-patients underwent 111In-pentetreotide-scintigraphy (24 h post-injection; planar+ single-photon emission CT (SPECT) abdomen) and whole-body 68Ga-DOTATOC-PET/CT. SPECT and PET were compared in a lesion-by-lesion and organ-by-organ analysis, determining the total lesions and ILs for both modalities. Results Significantly more lesions were detected on 68GaDOTATOC-PET/CT versus 111In-pentetreotide-scintigraphy. More specifically, we observed 1,098 lesions on PET/CT (range: 1–105; median: 15) versus 660 on SPECT (range: 0–73, median: 9) (p<0.0001), with 439 PET-ILs (42/53 patients) and one SPECT-IL (1/53 patients). The sensitivity for PET/CT was 99.9 % (95 % CI, 99.3–100.0), for SPECT 60.0 % (95 % CI, 48.5–70.2). The organ-by-organ analysis showed that the PET-ILs were most frequently visualized in liver and skeleton. Conclusion Ga-DOTATOC-PET/CT is superior for the detection of NET-metastases compared to 111In-pentetreotide SPECT. Key Points • Somatostatin receptor PET is superior to SPECT in detecting NET metastases • PET is the scintigraphic method for accurate depiction of NET tumour burden • The sensitivity of PET is twofold higher than the sensitivity of SPECT-
dc.language.isoen-
dc.rights© European Society of Radiology 2015-
dc.subject.other68Ga-DOTATOC; 111In-pentetreotide; SPECT; PRRT; neuroendocrine tumour-
dc.titleComparison of diagnostic accuracy of (111)In-pentetreotide SPECT and (68)Ga-DOTATOC PET/CT: A lesion-by-lesion analysis in patients with metastatic neuroendocrine tumours-
dc.typeJournal Contribution-
dc.identifier.epage909-
dc.identifier.issue3-
dc.identifier.spage900-
dc.identifier.volume26-
local.bibliographicCitation.jcatA1-
local.type.refereedRefereed-
local.type.specifiedArticle-
dc.identifier.doi10.1007/s00330-015-3882-1-
dc.identifier.isi000370158500035-
item.contributorVan Binnebeek, S.-
item.contributorVanbilloen, B.-
item.contributorBaete, K.-
item.contributorTerwinghe, C.-
item.contributorKoole, M.-
item.contributorMottaghy, F. M.-
item.contributorClement, P. M.-
item.contributorMortelmans, L.-
item.contributorBOGAERTS, Kris-
item.contributorHaustermans, K.-
item.contributorNackaerts, K.-
item.contributorVan Cutsem, E.-
item.contributorVerslype, C.-
item.contributorVerbruggen, A.-
item.contributorDeroose, C.-
item.fullcitationVan Binnebeek, S.; Vanbilloen, B.; Baete, K.; Terwinghe, C.; Koole, M.; Mottaghy, F. M.; Clement, P. M.; Mortelmans, L.; BOGAERTS, Kris; Haustermans, K.; Nackaerts, K.; Van Cutsem, E.; Verslype, C.; Verbruggen, A. & Deroose, C. (2016) Comparison of diagnostic accuracy of (111)In-pentetreotide SPECT and (68)Ga-DOTATOC PET/CT: A lesion-by-lesion analysis in patients with metastatic neuroendocrine tumours. In: EUROPEAN RADIOLOGY, 26(3), p. 900-909.-
item.accessRightsRestricted Access-
item.fulltextWith Fulltext-
item.validationecoom 2017-
crisitem.journal.issn0938-7994-
crisitem.journal.eissn1432-1084-
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