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dc.contributor.authorFountzilas, Georgeen
dc.contributor.authorCh, F. Tolisen
dc.contributor.authorKalogera-Fountzila, Annaen
dc.contributor.authorMisailidou, D.en
dc.contributor.authorTsekeris, P.en
dc.contributor.authorKarina, M.en
dc.contributor.authorNikolaou, A.en
dc.contributor.authorSamantas, E.en
dc.contributor.authorMakatsoris, T.en
dc.contributor.authorAthanassiou, E.en
dc.contributor.authorSkarlos, Dimosthenis V.en
dc.contributor.authorBamias, A. T.en
dc.contributor.authorZamboglou, N.en
dc.contributor.authorEconomopoulos, T.en
dc.contributor.authorKaranastassi, S.en
dc.contributor.authorPavlidis, Nicholasen
dc.contributor.authorDaniilidis, J.en
dc.creatorFountzilas, Georgeen
dc.creatorCh, F. Tolisen
dc.creatorKalogera-Fountzila, Annaen
dc.creatorMisailidou, D.en
dc.creatorTsekeris, P.en
dc.creatorKarina, M.en
dc.creatorNikolaou, A.en
dc.creatorSamantas, E.en
dc.creatorMakatsoris, T.en
dc.creatorAthanassiou, E.en
dc.creatorSkarlos, Dimosthenis V.en
dc.creatorBamias, A. T.en
dc.creatorZamboglou, N.en
dc.creatorEconomopoulos, T.en
dc.creatorKaranastassi, S.en
dc.creatorPavlidis, Nicholasen
dc.creatorDaniilidis, J.en
dc.date.accessioned2018-06-22T09:53:08Z
dc.date.available2018-06-22T09:53:08Z
dc.date.issued2005
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/41679
dc.description.abstractThe primary objective of this phase II study was to access the complete response (CR) rate to a new innovative induction regimen in patients with locally advanced head and neck cancer (LA-HNC). From October 2000 until October 2003 a total of 38 eligible patients (33 men and 5 women) entered the study. The large majority of them presented with a performance status of 0-1 and with clinical stage IV disease. Treatment consisted of three cycles of induction chemotherapy (IC) with paclitaxel 175 mg/m2 in a 3-h infusion on d 1, leucovorin (LV) 200 mg/m2 over 20 min immediately followed by FU 400 mg/m2 bolus and then 600 mg/m2 as a 24-h continuous infusion on d 1 and 2 and a cisplatin 75 mg/m2 over 1-h infusion on d 2 every 3 wk. This was then followed by radiation (70 Gy) and weekly cisplatin 40 mg/m2. After the completion of IC, 6/38 (16%) patients had CR. The CR rate was increased to 66% post-concomitant chemoradiotherapy (CCRT). Neutropenia (37.5%), pain (62%), nausea/vomiting (21%), and alopecia (79%) were the most frequent side effects during IC. The most pronounced toxicities during chemoradiotherapy were stomatitis (62.5%) and xerostomia (53%). Median time to progression was 11.0 mo and median survival 16.7 mo. One- and 2-yr survival rates were 73% and 38%, respectively. In conclusion, this novel induction regimen is active, is well tolerated, and can be successfully followed by CCRT with weekly cisplatin. CCRT should remain standard treatment for patients with LA-HNC. Novel induction combinations, such as that reported in the present study, should be evaluated in combination with CCRT only in the context of clinical trials. © Copyright 2005 by Humana Press Inc. All rights of any nature whatsoever reserved.en
dc.language.isoengen
dc.sourceMedical Oncologyen
dc.subjectArticleen
dc.subjectCisplatinen
dc.subjectFluorouracilen
dc.subjectHumanen
dc.subjectHumansen
dc.subjectAdulten
dc.subjectAgeden
dc.subjectControlled studyen
dc.subjectFemaleen
dc.subjectMiddle ageden
dc.subjectCancer growthen
dc.subjectCancer survivalen
dc.subjectChemotherapyen
dc.subjectFollow upen
dc.subjectPriority journalen
dc.subjectAlopeciaen
dc.subjectAnemiaen
dc.subjectAnorexiaen
dc.subjectAntineoplastic combined chemotherapy protocolsen
dc.subjectClinical articleen
dc.subjectClinical trialen
dc.subjectConstipationen
dc.subjectControlled clinical trialen
dc.subjectFatigueen
dc.subjectFebrile neutropeniaen
dc.subjectInfectionen
dc.subjectLeukopeniaen
dc.subjectMucosa inflammationen
dc.subjectMyalgiaen
dc.subjectNausea and vomitingen
dc.subjectNeurotoxicityen
dc.subjectNeutropeniaen
dc.subjectPhase 2 clinical trialen
dc.subjectRecombinant granulocyte colony stimulating factoren
dc.subjectStomatitisen
dc.subjectThrombocytopeniaen
dc.subjectTreatment outcomeen
dc.subjectInfusionsen
dc.subjectIntravenousen
dc.subjectCancer stagingen
dc.subjectDrug dose regimenen
dc.subjectPainen
dc.subjectFolinic aciden
dc.subjectCarcinomaen
dc.subjectMaleen
dc.subjectInjectionsen
dc.subjectSide effecten
dc.subjectLeucovorinen
dc.subjectBolus injectionen
dc.subjectContinuous infusionen
dc.subjectDysphagiaen
dc.subjectWeight reductionen
dc.subjectXerostomiaen
dc.subjectSquamous cellen
dc.subjectSquamous cell carcinomaen
dc.subjectPeripheral neuropathyen
dc.subjectPaclitaxelen
dc.subjectCombined modality therapyen
dc.subjectHypersensitivity reactionen
dc.subjectHead and neck neoplasmsen
dc.subjectHead and neck canceren
dc.subjectLaboratory testen
dc.subjectHead and neck carcinomaen
dc.subjectDermatitisen
dc.subjectHoarsenessen
dc.subjectOtitisen
dc.subjectPatient selectionen
dc.subjectTaste disorderen
dc.subjectTreatment withdrawalen
dc.titlePaclitaxel, cisplatin, leucovorin, and continuous infusion fluorouracil followed by concomitant chemoradiotherapy for locally advanced squamous cell carcinoma of the head and neck: A hellenic cooperative oncology group phase II studyen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1385/MO:22:3:269
dc.description.volume22
dc.description.issue3
dc.description.startingpage269
dc.description.endingpage279
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.orcidKalogera-Fountzila, Anna [0000-0002-6801-3129]
dc.gnosis.orcid0000-0002-2195-9961|0000-0002-6801-3129


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