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dc.contributor.authorFountzilas, Georgeen
dc.contributor.authorGossios, K.en
dc.contributor.authorZisiadis, A.en
dc.contributor.authorSvarna, E.en
dc.contributor.authorSkarlos, Dimosthenis V.en
dc.contributor.authorPavlidis, Nicholasen
dc.creatorFountzilas, Georgeen
dc.creatorGossios, K.en
dc.creatorZisiadis, A.en
dc.creatorSvarna, E.en
dc.creatorSkarlos, Dimosthenis V.en
dc.creatorPavlidis, Nicholasen
dc.date.accessioned2018-06-22T09:53:05Z
dc.date.available2018-06-22T09:53:05Z
dc.date.issued1996
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/41650
dc.description.abstractPossible prognostic variables for tumor response, time to progression (TTP), and survival in 141 patients with advanced colorectal cancer treated with fluorouracil and leucovorin-based chemotherapy were analyzed. None of the variables examined for their possible influence on tumor response attained significance in the stepwise logistic regression. In the univariate analysis, variables found to be strongly associated with TTP were performance status (PS) (P = 0.0301), liver involvement (P = 0.030), and the initial values of WBC (P = 0.0319), lactic dehydrogenase (LDH; P = 0.0053), γ- glutamyl-transpeptidase (γ-GT; P = 0.0013), alkaline phosphatase (ALP; P = 0.0186), albumin (P = 0.0004), and carcinoembryonic antigen (CEA; P = 0.0014). In the Cox analysis, liver involvement (P = 0.0553), albumin (P = 0.0181), PS (P =0.0484), and ALP (P = 0.0553) were retained as independently significant variables. When only patients with liver metastases were included in the analysis, then only albumin (P <0.001) demonstrated a prognostic significance. Also, in the univariate analysis, variables predicting survival were PS (P = 0.0230), grade (P = 0.0060), liver involvement (P = 0.0002), LDH (P = 0.0001), γ-GT (P < 0.001), ALP (P = 0.0006), albumin (P = 0.0309), and CEA (P = 0.0005).With the multivariate analysis, γ-GT (P = 0.0004), albumin (P = 0.0634), and CEA (P = 0.0804) were selected as significant. In those patients who presented with liver involvement, variables predicted survival were γ-GT (P = 0.0041), albumin (P = 0.0442), and the percentage of involved liver parenchyma (P =0.0690). These results could be helpful for the stratification of future trials in advanced colorectal cancer.en
dc.language.isoengen
dc.sourceMedical and pediatric oncologyen
dc.subjectArticleen
dc.subjectFluorouracilen
dc.subjectHumanen
dc.subjectHumansen
dc.subjectAdulten
dc.subjectAgeden
dc.subjectFemaleen
dc.subjectMajor clinical studyen
dc.subjectAdvanced canceren
dc.subjectCancer combination chemotherapyen
dc.subjectCancer survivalen
dc.subjectNeoplasm stagingen
dc.subjectPriority journalen
dc.subjectPrognosisen
dc.subjectRetrospective studiesen
dc.subjectRetrospective studyen
dc.subjectCancer stagingen
dc.subjectSurvival rateen
dc.subjectTreatment outcomeen
dc.subjectReviewen
dc.subjectMetastasisen
dc.subjectColorectal canceren
dc.subjectFolinic aciden
dc.subjectMaleen
dc.subjectMortalityen
dc.subjectRisk factorsen
dc.subjectClinical featureen
dc.subjectColorectal neoplasmsen
dc.subjectLeucovorinen
dc.subjectRisk factoren
dc.subjectPathologyen
dc.subjectMiddle ageden
dc.subjectAlkaline phosphataseen
dc.subjectLactate dehydrogenaseen
dc.subjectAntimetabolitesen
dc.subjectAntineoplasticen
dc.subjectChemotherapyen
dc.subjectCancer localizationen
dc.subjectCarcinoembryonic antigenen
dc.subjectAlbuminen
dc.subjectAlpha2b interferonen
dc.subjectAnalysis of varianceen
dc.subjectAntineoplastic antimetaboliteen
dc.subjectColorectal tumoren
dc.subjectDipyridamoleen
dc.subjectGamma glutamyltransferaseen
dc.subjectLaboratory testen
dc.subjectMedical recorden
dc.subjectPrognostic factorsen
dc.titlePrognostic variables in patients with advanced colorectal cancer treated with fluorouracil and leucovorin-based chemotherapyen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1002/(SICI)1096-911X(199605)26:5<305
dc.description.volume26
dc.description.issue5
dc.description.startingpage305
dc.description.endingpage317
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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