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dc.contributor.authorFountzilas, Georgeen
dc.contributor.authorPapakostas, P.en
dc.contributor.authorDafni, U.en
dc.contributor.authorMakatsoris, T.en
dc.contributor.authorKarina, M.en
dc.contributor.authorKalogera-Fountzila, Annaen
dc.contributor.authorManiadakis, N.en
dc.contributor.authorAravantinos, Gerasimosen
dc.contributor.authorSyrigos, K.en
dc.contributor.authorBamias, A. T.en
dc.contributor.authorChristodoulou, C.en
dc.contributor.authorEconomopoulos, T.en
dc.contributor.authorKalofonos, H. P.en
dc.contributor.authorNikolaou, A.en
dc.contributor.authorAngouridakis, N.en
dc.contributor.authorStathopoulos, G. P.en
dc.contributor.authorBafaloukos, Dimitriosen
dc.contributor.authorPavlidis, Nicholasen
dc.contributor.authorDaniilidis, J.en
dc.creatorFountzilas, Georgeen
dc.creatorPapakostas, P.en
dc.creatorDafni, U.en
dc.creatorMakatsoris, T.en
dc.creatorKarina, M.en
dc.creatorKalogera-Fountzila, Annaen
dc.creatorManiadakis, N.en
dc.creatorAravantinos, Gerasimosen
dc.creatorSyrigos, K.en
dc.creatorBamias, A. T.en
dc.creatorChristodoulou, C.en
dc.creatorEconomopoulos, T.en
dc.creatorKalofonos, H. P.en
dc.creatorNikolaou, A.en
dc.creatorAngouridakis, N.en
dc.creatorStathopoulos, G. P.en
dc.creatorBafaloukos, Dimitriosen
dc.creatorPavlidis, Nicholasen
dc.creatorDaniilidis, J.en
dc.date.accessioned2018-06-22T09:53:06Z
dc.date.available2018-06-22T09:53:06Z
dc.date.issued2006
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/41660
dc.description.abstractBackground: The prognosis of patients with recurrent and/or metastatic head and neck cancer (HNC) is poor. Median survival of these patients following chemotherapy is in the range of 6 to 9 months. In the present randomized phase III trial we compared two new combinations containing new drugs with proven activity in phase II studies with patients with HNC. Patients and methods: From November 1999 until November 2004, 166 eligible patients with HNC were enrolled in the study. They were treated with paclitaxel 175 mg/m2 on day 1 and gemcitabine 1000 mg/ m2 on days 1 and 8 every 3 weeks (group A, 85 patients) or with paclitaxel, as in group A, and pegylated liposomal doxorubicin 40 mg/m2 on day 1 every 4 weeks (group B, 81 patients). Results: There was no significant difference in response rate (20% versus 29%, P = 0.21), time to disease progression (median; 4.4 months versus 6.0 months, P = 0.09) and survival (median; 8.6 months versus 11.05 months, P = 0.25). Both regimens were generally well tolerated. The most frequently reported side effect, apart from alopecia, was neutropenia. Overall, there was no significant difference in severe toxicity between the two treatment arms. Conclusions: The present study could not demonstrate a survival benefit with either regimen. Both treatments were well tolerated. Randomized studies comparing each of the two regimens with standard chemotherapy are warranted. © 2006 Oxford University Press.en
dc.language.isoengen
dc.sourceAnnals of Oncologyen
dc.subjectGreeceen
dc.subjectArticleen
dc.subjectAntineoplastic agenten
dc.subjectHumanen
dc.subject80 and overen
dc.subjectAgeden
dc.subjectHumansen
dc.subjectAdulten
dc.subjectAgeden
dc.subjectCancer patienten
dc.subjectControlled studyen
dc.subjectFemaleen
dc.subjectMajor clinical studyen
dc.subjectMiddle ageden
dc.subjectAdvanced canceren
dc.subjectCancer survivalen
dc.subjectChemotherapyen
dc.subjectPriority journalen
dc.subjectAlopeciaen
dc.subjectAnemiaen
dc.subjectAntiemetic agenten
dc.subjectAntineoplastic combined chemotherapy protocolsen
dc.subjectArthralgiaen
dc.subjectClinical trialen
dc.subjectConstipationen
dc.subjectControlled clinical trialen
dc.subjectDiarrheaen
dc.subjectDrug efficacyen
dc.subjectFatigueen
dc.subjectFebrile neutropeniaen
dc.subjectInfectionen
dc.subjectLeukopeniaen
dc.subjectMucosa inflammationen
dc.subjectMyalgiaen
dc.subjectNeurotoxicityen
dc.subjectNeutropeniaen
dc.subjectOndansetronen
dc.subjectThrombocytopeniaen
dc.subjectSurvival analysisen
dc.subjectDexamethasoneen
dc.subjectDrug dose regimenen
dc.subjectDrug fatalityen
dc.subjectDrug hypersensitivityen
dc.subjectDrug tolerabilityen
dc.subjectGranulocyte colony stimulating factoren
dc.subjectPhase 3 clinical trialen
dc.subjectRandomized controlled trialen
dc.subjectStatistical significanceen
dc.subjectTreatment outcomeen
dc.subjectAntibiotic agenten
dc.subjectBisphosphonic acid derivativeen
dc.subjectCarcinomaen
dc.subjectMaleen
dc.subjectVomitingen
dc.subjectNauseaen
dc.subjectSurvival timeen
dc.subjectBone marrow toxicityen
dc.subjectGefitiniben
dc.subjectSquamous cellen
dc.subjectPeripheral neuropathyen
dc.subjectDeoxycytidineen
dc.subjectGemcitabineen
dc.subjectPaclitaxelen
dc.subjectPolyethylene glycolsen
dc.subjectBleeding disorderen
dc.subjectHand foot syndromeen
dc.subjectHealth care organizationen
dc.subjectHead and neck neoplasmsen
dc.subjectNasopharynx canceren
dc.subjectHead and neck canceren
dc.subjectPatient complianceen
dc.subjectAmifostineen
dc.subjectCost benefit analysisen
dc.subjectCost-benefit analysisen
dc.subjectDoxorubicinen
dc.subjectErythropoietinen
dc.subjectNew drugen
dc.subjectPyridoxineen
dc.subjectSensory neuropathyen
dc.titlePaclitaxel and gemcitabine vs. paclitaxel and pegylated liposomal doxorubicin in advanced non-nasopharyngeal head and neck cancer. An efficacy and cost analysis randomized study conducted by the Hellenic Cooperative Oncology Groupen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1093/annonc/mdl151
dc.description.volume17
dc.description.issue10
dc.description.startingpage1560
dc.description.endingpage1567
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.orcidAravantinos, Gerasimos [0000-0002-2106-1713]
dc.contributor.orcidKalogera-Fountzila, Anna [0000-0002-6801-3129]
dc.contributor.orcidKalofonos, H. P. [0000-0002-3286-778X]
dc.gnosis.orcid0000-0002-2195-9961
dc.gnosis.orcid0000-0002-2106-1713|0000-0002-6801-3129
dc.gnosis.orcid0000-0002-3286-778X


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