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dc.contributor.authorKalofonos, H. P.en
dc.contributor.authorKardamakis, D.en
dc.contributor.authorBamias, A. T.en
dc.contributor.authorSkarlos, Dimosthenis V.en
dc.contributor.authorPapakostas, P.en
dc.contributor.authorBafaloukos, Dimitriosen
dc.contributor.authorSakantamis, A.en
dc.contributor.authorPavlidis, Nicholasen
dc.contributor.authorFountzilas, Georgeen
dc.creatorKalofonos, H. P.en
dc.creatorKardamakis, D.en
dc.creatorBamias, A. T.en
dc.creatorSkarlos, Dimosthenis V.en
dc.creatorPapakostas, P.en
dc.creatorBafaloukos, Dimitriosen
dc.creatorSakantamis, A.en
dc.creatorPavlidis, Nicholasen
dc.creatorFountzilas, Georgeen
dc.date.accessioned2018-06-22T09:53:43Z
dc.date.available2018-06-22T09:53:43Z
dc.date.issued2003
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/41987
dc.description.abstractBackground: The addition of CPT-11 to 5FU/leucovorin resulted in survival benefit in patients with advanced colorectal cancer suggesting that this combination could be used successfully in the adjuvant setting. We studied the toxicity profile of postoperatively administered CPT-11 plus leucovorin (LV)-modulated 5FU and radiotherapy in patients with rectal cancer. Patients and Methods: Thirty-seven patients with Dukes' B2 and C rectal adenocarcinoma were treated with CPT-11, 80 mg/m2 ii.v. over 90 minutes followed by LV 200 mg/m2 over 2 hours and 5FU 450 mg/m2 i.v.-bolus weekly for 4 weeks followed by a 2-week rest period. One cycle included 4 infusions. The first cycle of chemotherapy was followed by pelvic radiation to a total dose of 45 Gy to the whole pelvis and a boost of 5 Gy to the tumor bed. 5FU was administered daily as a rapid infusion during the first 3 as well as the last 3 days of radiotherapy. CPT-11 plus LV-modulated 5FU was continued for a total of 6 cycles or consent withdrawal. Results: The main toxicity was reversible diarrhea (grade 3 and 4) in 9 (26%) patients during chemotherapy and in 3 (9%) patients during chemoradiotherapy. Furthermore, grade 3 leucopenia in 2 (6%) and 1 (3%) patient was observed during chemotherapy and chemoradio-therapy, respectively. Conclusion: This study provides evidence that adjuvant therapy using CPT-11 plus LV modulated 5FU and radiotherapy can be used in patients with rectal cancer.en
dc.language.isoengen
dc.sourceAnticancer Researchen
dc.subjectArticleen
dc.subjectFluorouracilen
dc.subjectHumanen
dc.subjectAdenocarcinomaen
dc.subjectHumansen
dc.subjectAdulten
dc.subjectAgeden
dc.subjectCancer patienten
dc.subjectControlled studyen
dc.subjectFemaleen
dc.subjectMiddle ageden
dc.subjectCancer combination chemotherapyen
dc.subjectChemotherapyen
dc.subjectNeoplasm stagingen
dc.subjectPriority journalen
dc.subjectAbdominal painen
dc.subjectAlopeciaen
dc.subjectAnemiaen
dc.subjectAntineoplastic combined chemotherapy protocolsen
dc.subjectClinical articleen
dc.subjectConstipationen
dc.subjectDiarrheaen
dc.subjectFatigueen
dc.subjectLeukopeniaen
dc.subjectMucosa inflammationen
dc.subjectNeutropeniaen
dc.subjectSkin diseaseen
dc.subjectThrombocytopeniaen
dc.subjectVertigoen
dc.subjectFeveren
dc.subjectPainen
dc.subjectCancer surgeryen
dc.subjectFeasibility studyen
dc.subjectCancer radiotherapyen
dc.subjectFolinic aciden
dc.subjectIrinotecanen
dc.subjectMaleen
dc.subjectAdjuvanten
dc.subjectVomitingen
dc.subjectRectal neoplasmsen
dc.subjectCancer adjuvant therapyen
dc.subjectLeucovorinen
dc.subjectRadiotherapyen
dc.subjectCamptothecinen
dc.subjectNauseaen
dc.subjectAdjuvant chemotherapyen
dc.subjectChemotherapy induced emesisen
dc.subjectEnteritisen
dc.subjectRectum hemorrhageen
dc.subjectFeasibility studiesen
dc.subjectHeadacheen
dc.subjectPostoperative careen
dc.subjectRectal canceren
dc.subjectRectum carcinomaen
dc.subjectPelvisen
dc.subjectRadiation doseen
dc.subjectSalivation disorderen
dc.titleAdjuvant chemotherapy using CPT-11, leucovorin plus bolus 5-fluorouracil and radiotherapy in patients with rectal cancer. A feasibility studyen
dc.typeinfo:eu-repo/semantics/article
dc.description.volume23
dc.description.issue2 Cen
dc.description.startingpage1687
dc.description.endingpage1691
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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