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dc.contributor.authorFountzilas, Georgeen
dc.contributor.authorStathopoulos, G. P.en
dc.contributor.authorKouvatseas, G.en
dc.contributor.authorPolychronis, A.en
dc.contributor.authorKlouvas, G. D.en
dc.contributor.authorSamantas, E.en
dc.contributor.authorZamboglou, N.en
dc.contributor.authorKyriakou, K.en
dc.contributor.authorAdamou, A.en
dc.contributor.authorPectasides, Dimitriosen
dc.contributor.authorEconomopoulos, T.en
dc.contributor.authorKalofonos, H. P.en
dc.contributor.authorBafaloukos, Dimitriosen
dc.contributor.authorGeorgoulias, V.en
dc.contributor.authorRazi, E. D.en
dc.contributor.authorKoukouras, D.en
dc.contributor.authorZombolas, V.en
dc.contributor.authorKosmidis, Paraskevas A.en
dc.contributor.authorSkarlos, Dimosthenis V.en
dc.contributor.authorPavlidis, Nicholasen
dc.creatorFountzilas, Georgeen
dc.creatorStathopoulos, G. P.en
dc.creatorKouvatseas, G.en
dc.creatorPolychronis, A.en
dc.creatorKlouvas, G. D.en
dc.creatorSamantas, E.en
dc.creatorZamboglou, N.en
dc.creatorKyriakou, K.en
dc.creatorAdamou, A.en
dc.creatorPectasides, Dimitriosen
dc.creatorEconomopoulos, T.en
dc.creatorKalofonos, H. P.en
dc.creatorBafaloukos, Dimitriosen
dc.creatorGeorgoulias, V.en
dc.creatorRazi, E. D.en
dc.creatorKoukouras, D.en
dc.creatorZombolas, V.en
dc.creatorKosmidis, Paraskevas A.en
dc.creatorSkarlos, Dimosthenis V.en
dc.creatorPavlidis, Nicholasen
dc.date.accessioned2018-06-22T09:53:08Z
dc.date.available2018-06-22T09:53:08Z
dc.date.issued2004
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/41676
dc.description.abstractThe present randomized phase III trial was designed to detect a 15% benefit in relapse-free survival (RFS) or overall survival (OS) from the incorporation of adjuvant tamoxifen to the combination of CNF [cyclophosphamide, 500 mg/m2; mitoxantrone (Novantrone), 10 mg/m2; fluorouracil, 500 mg/m2 chemotherapy and ovarian ablation in premenopausal patients with node-positive breast cancer and conversely from the incorporation of CNF chemotherapy to adjuvant tamoxifen in node-positive postmenopausal patients. From April 1992 until March 1998, 456 patients with operable breast cancer and one to nine infiltrated axillary nodes entered the study. Premenopausal patients were treated with six cycles of CNF chemotherapy followed by ovarian ablation with monthly injections of triptoreline 3.75 mg for 1 year (Group A, 84 patients) or the same treatment followed by 5 years of tamoxifen (Group B, 92 patients). Postmenopausal patients received 5 years of tamoxifen (Group C, 145 patients) or 6 cycles of CNF followed by 5 years of tamoxifen (Group D, 135 patients). Adjuvant radiation was administered to all patients with partial mastectomy. After a median follow-up period of 5 years, 125 patients (27%) relapsed and 79 (17%) died. The 5-year actuarial RFS for premenopausal patients was 65% in Group A and 68% in Group B (p = 0.86) and for postmenopausal patients 70% in Group C and 67% in Group D (p = 0.36). Also, the respective OS rates were 77% and 80% (p = 0.68) for premenopausal and 84% and 78% (p = 0.10) for postmenopausal patients. Severe toxicities were infrequently seen, with the exception of leukopenia (18%), among the 311 patients treated with CNF. In conclusion, the present study failed to demonstrate a 15% difference in RFS in favor of node-positive premenopausal patients treated with an additional 5 years of tamoxifen after CNF adjuvant chemotherapy and ovarian ablation. Similarly, six cycles of CNF preceding 5 years of tamoxifen did not translate to a 15% RFS benefit in node-positive postmenopausal patients.en
dc.language.isoengen
dc.sourceAmerican Journal of Clinical Oncology: Cancer Clinical Trialsen
dc.subjectArticleen
dc.subjectCyclophosphamideen
dc.subjectFluorouracilen
dc.subjectHumanen
dc.subjectNeoplasmsen
dc.subjectTamoxifenen
dc.subjectHumansen
dc.subjectAdulten
dc.subjectAgeden
dc.subjectBreast neoplasmsen
dc.subjectControlled studyen
dc.subjectFemaleen
dc.subjectMajor clinical studyen
dc.subjectMiddle ageden
dc.subjectCancer survivalen
dc.subjectFollow upen
dc.subjectAntineoplastic combined chemotherapy protocolsen
dc.subjectCancer recurrenceen
dc.subjectClinical trialen
dc.subjectControlled clinical trialen
dc.subjectLeukopeniaen
dc.subjectSurvival analysisen
dc.subjectPhase 3 clinical trialen
dc.subjectRandomized controlled trialen
dc.subjectTreatment outcomeen
dc.subjectLymphatic metastasisen
dc.subjectBreast canceren
dc.subjectCancer adjuvant therapyen
dc.subjectLymph node metastasisen
dc.subjectAdjuvant chemotherapyen
dc.subjectCancer therapyen
dc.subjectCombined modality therapyen
dc.subjectCancer hormone therapyen
dc.subjectTriptorelinen
dc.subjectPostmenopauseen
dc.subjectPartial mastectomyen
dc.subjectPremenopauseen
dc.subjectMitoxantroneen
dc.subjectHormone-dependenten
dc.subjectOvarian ablationen
dc.titleAdjuvant Cytotoxic and Endocrine Therapy in Pre- and Postmenopausal Patients with Breast Cancer and One to Nine Infiltrated Nodes: Five-Year Results of the Hellenic Cooperative Oncology Group Randomized HE 10/92 Studyen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1097/01.coc.0000046121.51504.B9
dc.description.volume27
dc.description.issue1
dc.description.startingpage57
dc.description.endingpage67
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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