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dc.contributor.authorBraadland, Peder
dc.contributor.authorGiskeødegård, Guro F.
dc.contributor.authorSandsmark, Elise
dc.contributor.authorBertilsson, Helena
dc.contributor.authorEuceda, Leslie R.
dc.contributor.authorHansen, Ailin Falkmo
dc.contributor.authorGuldvik, Ingrid Jenny
dc.contributor.authorSelnæs, Kirsten Margrete
dc.contributor.authorGrytli, Helene Hartvedt
dc.contributor.authorKatz, Betina
dc.contributor.authorSvindland, Aud
dc.contributor.authorBathen, Tone Frost
dc.contributor.authorEri, Lars Magne
dc.contributor.authorNygård, Ståle
dc.contributor.authorBerge, Viktor
dc.contributor.authorTasken, Kristin Austlid
dc.contributor.authorTessem, May-Britt
dc.date.accessioned2018-01-18T13:47:37Z
dc.date.available2018-01-18T13:47:37Z
dc.date.created2017-12-18T17:59:16Z
dc.date.issued2017
dc.identifier.citationBritish Journal of Cancer. 2017, 117 (11), 1656-1664.nb_NO
dc.identifier.issn0007-0920
dc.identifier.urihttp://hdl.handle.net/11250/2478175
dc.description.abstractBackground: Robust biomarkers that identify prostate cancer patients with high risk of recurrence will improve personalised cancer care. In this study, we investigated whether tissue metabolites detectable by high-resolution magic angle spinning magnetic resonance spectroscopy (HR-MAS MRS) were associated with recurrence following radical prostatectomy. Methods: We performed a retrospective ex vivo study using HR-MAS MRS on tissue samples from 110 radical prostatectomy specimens obtained from three different Norwegian cohorts collected between 2002 and 2010. At the time of analysis, 50 patients had experienced prostate cancer recurrence. Associations between metabolites, clinicopathological variables, and recurrence-free survival were evaluated using Cox proportional hazards regression modelling, Kaplan–Meier survival analyses and concordance index (C-index). Results: High intratumoural spermine and citrate concentrations were associated with longer recurrence-free survival, whereas high (total-choline+creatine)/spermine (tChoCre/Spm) and higher (total-choline+creatine)/citrate (tChoCre/Cit) ratios were associated with shorter time to recurrence. Spermine concentration and tChoCre/Spm were independently associated with recurrence in multivariate Cox proportional hazards modelling after adjusting for clinically relevant risk factors (C-index: 0.769; HR: 0.72; P=0.016 and C-index: 0.765; HR: 1.43; P=0.014, respectively). Conclusions: Spermine concentration and tChoCre/Spm ratio in prostatectomy specimens were independent prognostic markers of recurrence. These metabolites can be noninvasively measured in vivo and may thus offer predictive value to establish preoperative risk assessment nomograms.nb_NO
dc.language.isoengnb_NO
dc.publisherNature Publishing Groupnb_NO
dc.rightsNavngivelse-Ikkekommersiell-DelPåSammeVilkår 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/deed.no*
dc.titleEx vivo metabolic fingerprinting identifies biomarkers predictive of prostate cancer recurrence following radical prostatectomynb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber1656-1664nb_NO
dc.source.volume117nb_NO
dc.source.journalBritish Journal of Cancernb_NO
dc.source.issue11nb_NO
dc.identifier.doi10.1038/bjc.2017.346
dc.identifier.cristin1529272
dc.description.localcoder 2017 Cancer Research UK. All rights reserved 0007 – 0920/17. The authors' accepted and reviewed manuscript (post-print) is locked until 3 April 2018 due to copyright restrictions. The Publisher's version will become freely available on 3 October 2018 under a Creative Commons Attribution- NonCommercial-Share Alike 4.0 Unported License.nb_NO
cristin.unitcode194,65,25,0
cristin.unitcode194,65,15,0
cristin.unitnameInstitutt for sirkulasjon og bildediagnostikk
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.fulltextoriginal
cristin.qualitycode2


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Navngivelse-Ikkekommersiell-DelPåSammeVilkår 4.0 Internasjonal
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