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dc.contributor.authorBafaloukos, Dimitriosen
dc.contributor.authorPavlidis, Nicholasen
dc.contributor.authorFountzilas, Georgeen
dc.contributor.authorSkarlos, Dimosthenis V.en
dc.contributor.authorKlouvas, G. D.en
dc.contributor.authorMakrantonakis, P.en
dc.contributor.authorGiannakakis, T.en
dc.contributor.authorTsavaris, N.en
dc.contributor.authorKosmidis, Paraskevas A.en
dc.creatorBafaloukos, Dimitriosen
dc.creatorPavlidis, Nicholasen
dc.creatorFountzilas, Georgeen
dc.creatorSkarlos, Dimosthenis V.en
dc.creatorKlouvas, G. D.en
dc.creatorMakrantonakis, P.en
dc.creatorGiannakakis, T.en
dc.creatorTsavaris, N.en
dc.creatorKosmidis, Paraskevas A.en
dc.date.accessioned2018-06-22T09:52:31Z
dc.date.available2018-06-22T09:52:31Z
dc.date.issued1996
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/41391
dc.description.abstractThirty-four patients with advanced malignant melanoma were treated with recombinant alpha-interferon (IFN) and chemotherapy consisting of carboplatin, vinblastine, and bleomycin (CVB). CVB was given for four cycles and IFN for 1 year or until progression. Of the 34 analyzed patients. 17 (50%) achieved an objective response, including two complete (6%) and 15 partial responses (44%). Responses were noted in cutaneous, lymph node, and pulmonary sites, with a median time to disease progression of 5 months (range, 320 months). The median survival from onset of therapy was 8 months (range, 1-22 months) for the 34 patients. Ninety-four percent of the patients experienced flu-like symptoms and 82% fatigue or weakness. Leukopenia grade 3-4 was observed in four patients (12%). There were two toxicity-related deaths (6%); one from bleomycin-induced pneumonitis and one from neutropenic sepsis. It is concluded that the addition of IFN to CVB regimen, in this study, showed no apparent advantage on response rates, disease-free interval, or survival. The observed treatment-related mortality was unacceptably high. IFN administered as maintenance therapy following CVB confered no survival benefit.en
dc.language.isoengen
dc.sourceAmerican Journal of Clinical Oncology: Cancer Clinical Trialsen
dc.subjectArticleen
dc.subjectBleomycinen
dc.subjectHumanen
dc.subjectVinblastineen
dc.subjectHumansen
dc.subjectAdulten
dc.subjectAgeden
dc.subjectFemaleen
dc.subjectMiddle ageden
dc.subjectCancer survivalen
dc.subjectCarboplatinen
dc.subjectChemotherapyen
dc.subjectAntineoplastic combined chemotherapy protocolsen
dc.subjectClinical articleen
dc.subjectClinical trialen
dc.subjectFatigueen
dc.subjectLeukopeniaen
dc.subjectNeutropeniaen
dc.subjectProspective studiesen
dc.subjectThrombocytopeniaen
dc.subjectPneumoniaen
dc.subjectMelanomaen
dc.subjectMaleen
dc.subjectBlood cell counten
dc.subjectGastrointestinal symptomen
dc.subjectInterferonen
dc.subjectInterferon alfa-2aen
dc.subjectIntravenous drug administrationen
dc.subjectMaintenance therapyen
dc.subjectMalignant melanomaen
dc.subjectMortalityen
dc.subjectRecombinant alpha2a interferonen
dc.subjectSepsisen
dc.subjectSubcutaneous drug administrationen
dc.titleRecombinant interferon ALFA-2A in combination with carboplatin, vinblastine, and bleomycin in the treatment of advanced malignant melanomaen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1097/00000421-199606000-00018
dc.description.volume19
dc.description.issue3
dc.description.startingpage296
dc.description.endingpage300
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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