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dc.contributor.authorKosmidis, Paraskevas A.en
dc.contributor.authorSyrigos, K.en
dc.contributor.authorKalofonos, H. P.en
dc.contributor.authorDimopoulos, M. A.en
dc.contributor.authorSkarlos, Dimosthenis V.en
dc.contributor.authorPavlidis, Nicholasen
dc.contributor.authorBoukovinas, I.en
dc.contributor.authorBafaloukos, Dimitriosen
dc.contributor.authorPectasides, Dimitriosen
dc.contributor.authorBacoyiannis, Charalambosen
dc.contributor.authorFountzilas, Georgeen
dc.creatorKosmidis, Paraskevas A.en
dc.creatorSyrigos, K.en
dc.creatorKalofonos, H. P.en
dc.creatorDimopoulos, M. A.en
dc.creatorSkarlos, Dimosthenis V.en
dc.creatorPavlidis, Nicholasen
dc.creatorBoukovinas, I.en
dc.creatorBafaloukos, Dimitriosen
dc.creatorPectasides, Dimitriosen
dc.creatorBacoyiannis, Charalambosen
dc.creatorFountzilas, Georgeen
dc.date.accessioned2018-06-22T09:53:49Z
dc.date.available2018-06-22T09:53:49Z
dc.date.issued2012
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/42044
dc.description.abstractAim: The purpose of this study was to compare two single agents paclitaxel (intravenous) versus vinorelbine (oral) in non-small cell lung cancer (NSCLC) patients with performance status (PS):2. Patients and Methods: The patients were randomized to receive either oral vinorelbine 60 mg/m 2 on days I, 8, 15 every 4 weeks for 4 cycles (group A) or paclitaxel 90 mg/m 2 intravenously for 1 h on days 1, 8, 15 every 4 weeks for a total of 4 cycles (group B). Results: Among the 74 eligible patients (36 in arm A and 38 in arm B) in arm A, two (6%) had a partial response (95% Cl, 0.7-18.7) and 5 (14%) had stable disease (95% CI, 4.7-29.5). In arm B, five (13%) had a partial response (95% CI, 4.4-28.1) and 7 (18%) had stable disease (95% CI, 7.7-34.3). No significant difference was found in terms of clinical benefit between the two groups after two cycles of treatment except for appetite in favour of paclitaxel (p=0.01). Median survival was 3.1 months (95% CI, 2.2-4.0) for arm A and 5.1 months (95% CI, 2.7-7.6) for arm B (p=0.95). Toxicity was mild and only alopecia was more profound in the patients of arm B (p=0.008). Conclusion: No significant difference was found in clinical benefit between PS:2 NSCLC patients treated with either vinorelbine or paclitaxel.en
dc.language.isoengen
dc.sourceAnticancer Researchen
dc.subjectArticleen
dc.subjectCancer chemotherapyen
dc.subjectHumanen
dc.subject80 and overen
dc.subjectAdenocarcinomaen
dc.subjectAgeden
dc.subjectBrain neoplasmsen
dc.subjectHumansen
dc.subjectAdulten
dc.subjectControlled studyen
dc.subjectFemaleen
dc.subjectMajor clinical studyen
dc.subjectMiddle ageden
dc.subjectAdvanced canceren
dc.subjectChemotherapyen
dc.subjectDisease progressionen
dc.subjectNeoplasm stagingen
dc.subjectPriority journalen
dc.subjectAlopeciaen
dc.subjectAnemiaen
dc.subjectAntineoplastic combined chemotherapy protocolsen
dc.subjectDiarrheaen
dc.subjectLeukopeniaen
dc.subjectLocalen
dc.subjectNavelbineen
dc.subjectNeoplasm recurrenceen
dc.subjectNeutropeniaen
dc.subjectStomatitisen
dc.subjectThrombocytopeniaen
dc.subjectTreatment outcomeen
dc.subjectVinblastineen
dc.subjectVinorelbineen
dc.subjectFeveren
dc.subjectLiver toxicityen
dc.subjectPainen
dc.subjectRandomized controlled trialen
dc.subjectLung neoplasmsen
dc.subjectLung non small cell canceren
dc.subjectSurvival rateen
dc.subjectCarcinomaen
dc.subjectMaleen
dc.subjectBleedingen
dc.subjectVomitingen
dc.subjectFollow-up studiesen
dc.subjectLymphatic metastasisen
dc.subjectLiver neoplasmsen
dc.subjectMultiple cycle treatmenten
dc.subjectDrug withdrawalen
dc.subjectSquamous cellen
dc.subjectPaclitaxelen
dc.subjectBone neoplasmsen
dc.subjectHistamine h2 receptor antagonisten
dc.subjectPruritusen
dc.subjectNon-small-cell lungen
dc.subjectLymphocytopeniaen
dc.subjectRashen
dc.subjectClinical benefiten
dc.subjectLarge cellen
dc.subjectLung infectionen
dc.subjectNon-small cell lung canceren
dc.subjectPerformance status of 2en
dc.subjectSmall cell lung carcinomaen
dc.titleVinorelbine versus paclitaxel for patients with advanced non-small cell lung cancer (NSCLC) and a performance status of 2en
dc.typeinfo:eu-repo/semantics/article
dc.description.volume32
dc.description.issue1
dc.description.startingpage175
dc.description.endingpage181
dc.author.facultyΙατρική Σχολή / Medical School
dc.author.departmentΙατρική Σχολή / Medical School
dc.type.uhtypeArticleen
dc.contributor.orcidPavlidis, Nicholas [0000-0002-2195-9961]
dc.contributor.orcidKalofonos, H. P. [0000-0002-3286-778X]
dc.gnosis.orcid0000-0002-2195-9961
dc.gnosis.orcid0000-0002-3286-778X


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