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dc.contributor.authorKosmidis, Paraskevas A.en
dc.contributor.authorMylonakis, N.en
dc.contributor.authorDimopoulos, M. A.en
dc.contributor.authorPavlidis, Nicholasen
dc.contributor.authorFountzilas, Georgeen
dc.contributor.authorSamantas, E.en
dc.contributor.authorDimitriadis, K.en
dc.contributor.authorKalofonos, H. P.en
dc.contributor.authorTsavdaridis, D.en
dc.contributor.authorSkarlos, Dimosthenis V.en
dc.creatorKosmidis, Paraskevas A.en
dc.creatorMylonakis, N.en
dc.creatorDimopoulos, M. A.en
dc.creatorPavlidis, Nicholasen
dc.creatorFountzilas, Georgeen
dc.creatorSamantas, E.en
dc.creatorDimitriadis, K.en
dc.creatorKalofonos, H. P.en
dc.creatorTsavdaridis, D.en
dc.creatorSkarlos, Dimosthenis V.en
dc.date.accessioned2018-06-22T09:53:48Z
dc.date.available2018-06-22T09:53:48Z
dc.date.issued2000
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/42037
dc.description.abstractGemcitabine plus paclitaxel and paclitaxel plus carboplatin are active and well tolerated in patients with advanced non-small cell lung cancer, showing similar rates of response and survival. The Hellenic Cooperative Oncology Group conducted a randomized phase III trial comparing gemcitabine plus paclitaxel with paclitaxel plus carboplatin. Patients were randomly assigned to two groups. Group A received paclitaxel 200 mg/m2 plus carboplatin (area under the curve = 6) on day I. Group B received paclitaxel in identical fashion to group A plus gemcitabine 1,000 mg/m2 on days 1 and 8 every 3 weeks. A minimum of two cycles and a maximum of six cycles was allowed. To date, 127 eligible patients (63 in group A and 64 in group B) have been randomized; the median follow-up time is 4.6 months. Preliminary results suggest that both combinations can be given in full doses and are well tolerated. Grade 3/4 neutropenia was mild but more prominent in group A (10% v 3%, respectively) while thrombocytopenia was not significant for either group. Moreover, severe neurotoxicity, hepatotoxicity, or cardiac toxicity has not been observed in the vast majority of patients in either group. Although patients in group B experienced higher response rates (37.5%) than those in group A (21.8%), the difference between the groups was not statistically significant. Definite conclusions about this study cannot be made until more data are available. Copyright (C) 2000 by W.B. Saunders Company.en
dc.language.isoengen
dc.sourceSeminars in oncologyen
dc.subjectArticleen
dc.subjectAdulten
dc.subjectHumanen
dc.subjectAgeden
dc.subjectHumansen
dc.subjectControlled studyen
dc.subjectFemaleen
dc.subjectMajor clinical studyen
dc.subjectMiddle ageden
dc.subjectCancer combination chemotherapyen
dc.subjectCarboplatinen
dc.subjectFollow upen
dc.subjectPaclitaxelen
dc.subjectPriority journalen
dc.subjectAntineoplastic combined chemotherapy protocolsen
dc.subjectClinical trialen
dc.subjectControlled clinical trialen
dc.subjectGemcitabineen
dc.subjectNeurotoxicityen
dc.subjectNeutropeniaen
dc.subjectThrombocytopeniaen
dc.subjectSurvival analysisen
dc.subjectArea under the curveen
dc.subjectCardiotoxicityen
dc.subjectLiver toxicityen
dc.subjectPhase 3 clinical trialen
dc.subjectRandomized controlled trialen
dc.subjectSurvival rateen
dc.subjectLung neoplasmsen
dc.subjectLung non small cell canceren
dc.subjectCarcinomaen
dc.subjectMaleen
dc.subjectDeoxycytidineen
dc.subjectNon-small-cell lungen
dc.titleCombination chemotherapy with paclitaxel plus carboplatin versus paclitaxel plus gemcitabine in inoperable non-small cell lung cancer: A phase III randomized study. Preliminary resultsen
dc.typeinfo:eu-repo/semantics/article
dc.description.volume27
dc.description.issue1 SUPPL. 1en
dc.description.startingpage3
dc.description.endingpage8
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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