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dc.contributor.authorKosmidis, Paraskevas A.en
dc.contributor.authorTsavaris, N.en
dc.contributor.authorSkarlos, Dimosthenis V.en
dc.contributor.authorTheocharis, D.en
dc.contributor.authorSamantas, E.en
dc.contributor.authorPavlidis, Nicholasen
dc.contributor.authorBriassoulis, E. Chen
dc.contributor.authorFountzilas, Georgeen
dc.creatorKosmidis, Paraskevas A.en
dc.creatorTsavaris, N.en
dc.creatorSkarlos, Dimosthenis V.en
dc.creatorTheocharis, D.en
dc.creatorSamantas, E.en
dc.creatorPavlidis, Nicholasen
dc.creatorBriassoulis, E. Chen
dc.creatorFountzilas, Georgeen
dc.date.accessioned2018-06-22T09:53:50Z
dc.date.available2018-06-22T09:53:50Z
dc.date.issued1996
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/42045
dc.description.abstractPurpose: To investigate if double modulation of fluorouracil (5-FU) with leucovorin (folinic acid [FA]) and interferon alfa-2b (IFN 2b) improves responses and survival in comparison to single modulation of 5-FU with FA. Patients and Methods: One hundred six patients with histologically confirmed advanced colorectal cancer, measurable disease, and without previous chemotherapy were prospectively randomized into two groups. Patients in group A received 5-FU 450 mg/m2 as an intravenous bolus in the midinfusion of FA weekly. FA was given at a dose of 200 mg/m2 in 500 mL 0.9% normal saline solution in 2-hour infusion. Patients in group B received exactly the same regimen plus IFN 2b 5 million units subcutaneously three times weekly. Results: All patients were well balanced in both groups regarding age, sex, performance status, number, and site of metastasis. One hundred two patients were assessable. All patients have died. There was no difference in response between the two groups (7.8% v 9.8%). Median survival was 10.1 months in group A, and 7.2 months in group B (P = .00189). Median time to progression was 8.4 and 5.2 months, respectively (P = .00196). Overall, better performance status and older age had a positive impact on survival. Toxicity was the most important and catastrophic aspect of this study. Patients who received IFN 2b had significantly worse anemia, neutropenia, diarrhea, anorexia, weight loss, flu-like syndrome, and psychological reactions. Conclusion: Based on this final analysis, the addition of IFN 2b to the combination of 5-FU and FA enhances toxicity and contributes to decreased survival.en
dc.language.isoengen
dc.sourceJournal of Clinical Oncologyen
dc.subjectArticleen
dc.subjectFluorouracilen
dc.subjectHumanen
dc.subjectHumansen
dc.subjectAdulten
dc.subjectAgeden
dc.subjectControlled studyen
dc.subjectFemaleen
dc.subjectMajor clinical studyen
dc.subjectMiddle ageden
dc.subjectAdvanced canceren
dc.subjectCancer combination chemotherapyen
dc.subjectCancer survivalen
dc.subjectPriority journalen
dc.subjectAntineoplastic combined chemotherapy protocolsen
dc.subjectClinical trialen
dc.subjectControlled clinical trialen
dc.subjectDisease-free survivalen
dc.subjectProspective studiesen
dc.subjectThrombocytopeniaen
dc.subjectAntineoplastic activityen
dc.subjectGastrointestinal toxicityen
dc.subjectPhase 3 clinical trialen
dc.subjectRandomized controlled trialen
dc.subjectTreatment outcomeen
dc.subjectColorectal canceren
dc.subjectFolinic aciden
dc.subjectGranulocytopeniaen
dc.subjectMaleen
dc.subjectSubcutaneous drug administrationen
dc.subjectRectal neoplasmsen
dc.subjectLeucovorinen
dc.subjectAlpha2b interferonen
dc.subjectColonic neoplasmsen
dc.subjectInterferon alfa-2ben
dc.subjectAntidotesen
dc.titleFluorouracil and leucovorin with or without interferon alfa-2b in advanced colorectal cancer: Analysis of a prospective randomized phase III trialen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1200/JCO.1996.14.10.2682
dc.description.volume14
dc.description.issue10
dc.description.startingpage2682
dc.description.endingpage2687
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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