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dc.contributor.authorLiposits, Gabor
dc.contributor.authorSkuladottir, Halla
dc.contributor.authorRyg, Jesper
dc.contributor.authorWinther, Stine Brændegaard
dc.contributor.authorMöller, Sören
dc.contributor.authorHofsli, Eva
dc.contributor.authorShah, Carl-Henrik
dc.contributor.authorPoulsen, Laurids Østergaard
dc.contributor.authorBerglund, Åke
dc.contributor.authorQvortrup, Camilla
dc.contributor.authorOsterlund, Pia
dc.contributor.authorJohansen, Julia S.
dc.contributor.authorGlimelius, Bengt
dc.contributor.authorSorbye, Halfdan
dc.contributor.authorPfeiffer, Per
dc.date.accessioned2023-01-11T10:19:27Z
dc.date.available2023-01-11T10:19:27Z
dc.date.created2022-10-30T13:11:15Z
dc.date.issued2022
dc.identifier.issn2077-0383
dc.identifier.urihttps://hdl.handle.net/11250/3042641
dc.description.abstractAppropriate patient selection for palliative chemotherapy is crucial in patients with metastatic colorectal cancer (mCRC). We investigated the prognostic value of C-reactive protein (CRP), derived neutrophil-to-lymphocyte ratio (dNLR), Interleukin (IL)-6, and YKL-40 on progression-free survival (PFS) and overall survival (OS) in the NORDIC9 cohort. The randomized NORDIC9-study included patients ≥70 years with mCRC not candidates for standard full-dose combination chemotherapy. Participants received either full-dose S1 (Teysuno) or a dose-reduced S1 plus oxaliplatin. Blood samples were collected at baseline and biomarkers were dichotomized according to standard cut-offs. Multivariable analyses adjusted for age, sex, ECOG performance status, and treatment allocation; furthermore, C-statistics were estimated. In total, 160 patients with a median age of 78 years (IQR: 76–81) were included between 2015 and 2017. All investigated biomarkers were significantly elevated in patients with either weight loss, ≥3 metastatic sites, or primary tumor in situ. In multivariable analyses, all markers showed significant association with OS; the highest HR was observed for CRP (HR = 3.40, 95%CI: 2.20–5.26, p < 0.001). Regarding PFS, statistically significant differences were found for CRP and IL-6, but not for dNLR and YKL-40. Applying C-statistics, CRP indicated a good prognostic model for OS (AUC = 0.72, 95%CI: 0.67–0.76). CRP is an easily available biomarker, which may support therapeutic decision-making in vulnerable older patients with mCRC.en_US
dc.language.isoengen_US
dc.publisherMDPIen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleThe prognostic value of pre-treatment circulating biomarkers of systemic inflammation (CRP, dNLR, YKL-40, and IL-6) in vulnerable older patients with metastatic colorectal cancer receiving palliative chemotherapy—The Randomized NORDIC9-Studyen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2022 The Author(s)en_US
dc.source.articlenumber5603en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.3390/jcm11195603
dc.identifier.cristin2066439
dc.source.journalJournal of Clinical Medicineen_US
dc.identifier.citationJournal of Clinical Medicine. 2022, 11 (19), 5603.en_US
dc.source.volume11en_US
dc.source.issue19en_US


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Navngivelse 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Navngivelse 4.0 Internasjonal