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dc.contributor.authorThomsen, Maria
dc.contributor.authorSkovlund, Eva
dc.contributor.authorSorbye, Halfdan
dc.contributor.authorBolstad, Nils
dc.contributor.authorNustad, Kjell Johannes
dc.contributor.authorGlimelius, Bengt
dc.contributor.authorPfeiffer, Per
dc.contributor.authorKure, Elin Wenche Hegland
dc.contributor.authorJohansen, Julia S.
dc.contributor.authorTveit, Magne Kjell
dc.contributor.authorChristoffersen, Thoralf
dc.contributor.authorGuren, Tormod Kyrre
dc.date.accessioned2019-01-29T15:17:33Z
dc.date.available2019-01-29T15:17:33Z
dc.date.created2018-06-23T12:40:14Z
dc.date.issued2018
dc.identifier.citationBritish Journal of Cancer. 2018, 118 (12), 1609-1616.nb_NO
dc.identifier.issn0007-0920
dc.identifier.urihttp://hdl.handle.net/11250/2582930
dc.description.abstractBackground Mutation status of RAS and BRAF, as well as serum levels of carcinoembryonic antigen (CEA) and carbohydrate antigen 19-9 (CA 19-9), are biomarkers used in clinical management of patients with gastrointestinal cancers. This study aimed to examine the prognostic role of these biomarkers in a patient population that started first-line chemotherapy for unresectable metastatic colorectal cancer (mCRC) in the NORDIC-VII study. Methods CEA and CA 19-9 were measured in serum samples from 545 patients obtained before the start of chemotherapy. Four hundred and ninety-four patients had detectable levels of carbohydrate antigen 19-9 (CA 19-9). RAS (exons 2–4) and BRAF (V600E) mutation status were available from 440 patients. Overall survival (OS) was estimated in patient groups defined by serum CEA or CA 19-9 levels using cut-off values of 5 µg/L and 35 kU/L, respectively, in the total population and in subgroups according to RAS and BRAF mutation status. Results For both CEA and CA 19-9, elevated serum levels were associated with reduced OS in adjusted analyses which included RAS and BRAF mutation status, baseline World Health Organization performance status, and levels of alkaline phosphatase and C-reactive protein. The negative prognostic information provided by an elevated CA 19-9 level was particularly marked in patients with BRAF mutation (hazard ratio = 4.35, interaction P = 0.003, in an adjusted model for OS). Conclusions High baseline serum concentrations of CEA and CA 19-9 provide independent information of impaired prognosis in mCRC. In patients with BRAF-mutant tumours, elevated serum CA 19-9 may identify a subgroup with highly aggressive disease and could contribute to improving therapeutic decisions.nb_NO
dc.language.isoengnb_NO
dc.publisherSpringer Naturenb_NO
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titlePrognostic role of carcinoembryonic antigen and carbohydrate antigen 19-9 in metastatic colorectal cancer: a BRAF-mutant subset with high CA 19-9 level and poor outcomenb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber1609-1616nb_NO
dc.source.volume118nb_NO
dc.source.journalBritish Journal of Cancernb_NO
dc.source.issue12nb_NO
dc.identifier.doi10.1038/s41416-018-0115-9
dc.identifier.cristin1593416
dc.description.localcodeThis is a published version of an article published in British Journal of Cancer. Locked until 6.6.2019 due to copyright restrictions. The final authenticated version is available online at:https://doi.org/10.1038/s41416-018-0115-9nb_NO
cristin.unitcode194,65,20,0
cristin.unitnameInstitutt for samfunnsmedisin og sykepleie
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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