Is there any correlation between levels of serum ostepontin, CEA, and FDG uptake in lung cancer patients with bone metastasis?

dc.authorid0000-0002-2645-7661
dc.authorid0000-0002-9132-9092
dc.contributor.authorAyan, A. K.
dc.contributor.authorErdemci, B.
dc.contributor.authorOrsal, E.
dc.contributor.authorBayraktutan, Z.
dc.contributor.authorAkpinar, E.
dc.contributor.authorTopcu, A.
dc.contributor.authorTurkeli, M.
dc.date.accessioned2025-05-10T19:43:29Z
dc.date.issued2016
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractObjective: In this study, an evaluation was made of the relationship between the serum levels of carcinoembryonic antigen (CEA), osteopontin (OPN), and the semi-quantitative parameters of 18-fluoro2-deoxyglucose positron emission tomography/computed tomography (F-18-FDG PET/CT) in lung cancer patients with bone metastasis. Material and methods: The evaluation included 42 non-small cell lung cancer (NSCLC) and 31 small cell lung cancer (SCLC) patients who were referred to our institution for staging by F-18-FDG PET/CT. The biochemical parameters measured included CEA and OPN serum levels. Results: Serum levels of OPN in NSCLC patients with and without bone metastasis were 21.20 +/- 4.97 ng/ml and 13.33 +/- 4.53 ng/ml, respectively (p < 0.05). In SCLC patients with and without bone metastasis serum OPN levels were 23.95 +/- 4.78 ng/ml and 17.30 +/- 3.09 ng/ml, respectively (p < 0.05). Serum levels of CEA in NSCLC patients with and without bone metastasis were 33.79 +/- 6.49 ng/ml and 11.74 +/- 2.96 ng/ml, respectively (p < 0.05). In SCLC patients with and without bone metastasis serum levels of CEA were 28.93 +/- 4.59 ng/ml and 13.88 +/- 4.47 ng/ml, respectively (p < 0.05). There were no correlations between primary tumor SUVmax, and serum levels of CEA and OPN. Conclusions: Bone metastasis can be detected in patients with lung cancer by measuring CEA and OPN levels. Increased levels of CEA and OPN levels may be considered an early warning sign in patients needing accurate imaging, as they are at higher risk of bone metastasis. (C) 2015 Elsevier Espana, S.L.U. and SEMNIM. All rights reserved.
dc.identifier.doi10.1016/j.remn.2015.09.002
dc.identifier.endpage106
dc.identifier.issn2253-654X
dc.identifier.issue2
dc.identifier.pmid26521996
dc.identifier.scopus2-s2.0-84958178865
dc.identifier.scopusqualityQ4
dc.identifier.startpage102
dc.identifier.urihttps://doi.org/10.1016/j.remn.2015.09.002
dc.identifier.urihttps://hdl.handle.net/20.500.14730/10621
dc.identifier.volume35
dc.identifier.wosWOS:000371940100006
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherElsevier Espana Slu
dc.relation.ispartofRevista Espanola De Medicina Nuclear E Imagen Molecular
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20250302
dc.subjectLung cancer
dc.subjectBone metastasis
dc.subjectPositron emission tomography
dc.subjectCEA
dc.subjectOPN
dc.titleIs there any correlation between levels of serum ostepontin, CEA, and FDG uptake in lung cancer patients with bone metastasis?
dc.typeArticle

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