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dc.contributor.authorPavlidis, Nicholasen
dc.contributor.authorKalef-Ezra, J. A.en
dc.contributor.authorBriassoulis, E. Chen
dc.contributor.authorSkarlos, Dimosthenis V.en
dc.contributor.authorKosmidis, Paraskevas A.en
dc.contributor.authorSaferiadis, K.en
dc.contributor.authorBairaktari, Eleni Then
dc.contributor.authorBafaloukos, Dimitriosen
dc.contributor.authorMaravegias, A.en
dc.contributor.authorTheoharis, D.en
dc.contributor.authorFountzilas, Georgeen
dc.creatorPavlidis, Nicholasen
dc.creatorKalef-Ezra, J. A.en
dc.creatorBriassoulis, E. Chen
dc.creatorSkarlos, Dimosthenis V.en
dc.creatorKosmidis, Paraskevas A.en
dc.creatorSaferiadis, K.en
dc.creatorBairaktari, Eleni Then
dc.creatorBafaloukos, Dimitriosen
dc.creatorMaravegias, A.en
dc.creatorTheoharis, D.en
dc.creatorFountzilas, Georgeen
dc.date.accessioned2018-06-22T09:54:18Z
dc.date.available2018-06-22T09:54:18Z
dc.date.issued1994
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/42289
dc.description.abstractWe have retrospectively evaluated six serum tumor markers in 85 patients with carcinoma of unknown primary. The serum levels of carcinoembryonic antigen (CEA), CA 19‐9, CA 15‐3, CA 125, β‐chorionic gonadotropin (β‐HCG) and α‐fetoprotein (AFP) were related with the histological pattern (undifferentiated carcinoma or adenocarcinoma), the number and the site of metastases, as well as the response to chemotherapy and the patients' survival. More than 40% of the patients had increased serum levels of all six tumor markers, except of AFP which was found to be increased in only 17% of them. Increased levels of CA 19‐9 were related to metastatic adenocarcinoma, whereas CA 19‐9 and CA 15‐3 had a relationship with more advanced disease. Patients with liver involvement had higher mean levels of CEA and CA 19‐9 as compared to those with nodal disease. None of these markers was found to have a predictive value for response to chemotherapy or survival. Although the present study has a retrospective nature, it allows us to conclude that patients with CUP have a nonspecific over‐expression of the above serum tumor markers and that routine use of these markers does not offer any diagnostic or prognostic assistance. © 1994 wiley‐Liss, lnc. Copyright © 1994 Wiley‐Liss, Inc., A Wiley Companyen
dc.language.isoengen
dc.sourceMedical and pediatric oncologyen
dc.subjectArticleen
dc.subjectHumanen
dc.subjectNeoplasmsen
dc.subjectAdulten
dc.subjectFemaleen
dc.subjectMajor clinical studyen
dc.subjectAdvanced canceren
dc.subjectCancer survivalen
dc.subjectNeoplasmen
dc.subjectPredictive value of testsen
dc.subjectPriority journalen
dc.subjectPrognosisen
dc.subjectRetrospective studiesen
dc.subjectLung neoplasmsen
dc.subjectSurvival rateen
dc.subjectCarcinomaen
dc.subjectMaleen
dc.subjectAntigensen
dc.subjectLymph node metastasisen
dc.subjectLiver neoplasmsen
dc.subjectLiver metastasisen
dc.subjectAdenocarcinomaen
dc.subjectBiologicalen
dc.subjectTumor markersen
dc.subjectUnknown primaryen
dc.subjectCancer localizationen
dc.subjectUndifferentiated carcinomaen
dc.subjectBone neoplasmsen
dc.subjectMiddle ageen
dc.subjectAlpha fetoproteinen
dc.subjectChorionic gonadotropin beta subuniten
dc.subjectCarcinoembryonic antigenen
dc.subjectCarcinoma of unknown primaryen
dc.subjectLinear modelsen
dc.subjectLymph nodesen
dc.subjectCa 125 antigenen
dc.subjectCa 15-3 antigenen
dc.subjectCa 19-9 antigenen
dc.subjectAlpha-fetoproteinsen
dc.subjectAntigen expressionen
dc.subjectCarbohydrateen
dc.subjectCentral nervous system neoplasmsen
dc.subjectChorionic gonadotropinen
dc.subjectPeritoneal neoplasmsen
dc.subjectSerum tumor markersen
dc.subjectTumor-associateden
dc.titleEvaluation of six tumor markers in patients with carcinoma of unknown primaryen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1002/mpo.2950220303
dc.description.volume22
dc.description.issue3
dc.description.startingpage162
dc.description.endingpage167
dc.author.facultyΙατρική Σχολή / Medical School
dc.author.departmentΙατρική Σχολή / Medical School
dc.type.uhtypeArticleen
dc.contributor.orcidPavlidis, Nicholas [0000-0002-2195-9961]
dc.gnosis.orcid0000-0002-2195-9961


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