Show simple item record

dc.contributor.authorFountzilas, Georgeen
dc.contributor.authorNikolaides, C.en
dc.contributor.authorAravantinos, Gerasimosen
dc.contributor.authorSkarlos, Dimosthenis V.en
dc.contributor.authorKosmidis, Paraskevas A.en
dc.contributor.authorPapakostas, P.en
dc.contributor.authorStathopoulos, G. P.en
dc.contributor.authorKontostolis, E.en
dc.contributor.authorBafaloukos, Dimitriosen
dc.contributor.authorPavlidis, Nicholasen
dc.creatorFountzilas, Georgeen
dc.creatorNikolaides, C.en
dc.creatorAravantinos, Gerasimosen
dc.creatorSkarlos, Dimosthenis V.en
dc.creatorKosmidis, Paraskevas A.en
dc.creatorPapakostas, P.en
dc.creatorStathopoulos, G. P.en
dc.creatorKontostolis, E.en
dc.creatorBafaloukos, Dimitriosen
dc.creatorPavlidis, Nicholasen
dc.date.accessioned2018-06-22T09:53:05Z
dc.date.available2018-06-22T09:53:05Z
dc.date.issued1998
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/41652
dc.description.abstractForty-one patients with operable breast cancer and ≥ 10 positive axillary lymph nodes were treated with 6 cycles of dose-dense adjuvant chemotherapy consisting of epirubicin (100 mg/m2) every 2 weeks with G-CSF support. A total of 240 cycles were administered, all of them at full dose and 19 (8%) with a delay. Thirty-eight (93%) patients completed the treatment according to the protocol. The relative dose intensity of epirubicin was 0.99. Grade 3 toxicities included anemia (3%), nausea and vomiting (5%) and alopecia (71%). After a median fellow-up of 40 months, 16 (39%) patients were free of relapse. In conclusion, the present study has shown that the administration of dose-dense chemotherapy with epirubicin is feasible in the adjuvant setting with minimal toxicity.en
dc.language.isoengen
dc.sourceOncologyen
dc.subjectArticleen
dc.subjectHumanen
dc.subjectHumansen
dc.subjectAdulten
dc.subjectAgeden
dc.subjectBreast neoplasmsen
dc.subjectFemaleen
dc.subjectMiddle ageden
dc.subjectPriority journalen
dc.subjectAlopeciaen
dc.subjectAnemiaen
dc.subjectClinical articleen
dc.subjectClinical trialen
dc.subjectGranulocyte colony-stimulating factoren
dc.subjectRecombinant granulocyte colony stimulating factoren
dc.subjectDrug administration scheduleen
dc.subjectFeasibility studyen
dc.subjectDose responseen
dc.subjectDose-response relationshipen
dc.subjectDrugen
dc.subjectIntravenous drug administrationen
dc.subjectSubcutaneous drug administrationen
dc.subjectVomitingen
dc.subjectFollow-up studiesen
dc.subjectLymphatic metastasisen
dc.subjectAxillary lymph nodeen
dc.subjectBreast canceren
dc.subjectCancer adjuvant therapyen
dc.subjectLymph node metastasisen
dc.subjectNauseaen
dc.subjectAdjuvant chemotherapyen
dc.subjectAntineoplasticen
dc.subjectCombined modality therapyen
dc.subjectFeasibility studiesen
dc.subjectClinical protocolen
dc.subjectEpirubicinen
dc.subjectAntibioticsen
dc.titleDose-dense adjuvant chemotherapy with epirubicin monotherapy in patients with operable breast cancer and ≥ 10 positive axillary lymph nodesen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1159/000011903
dc.description.volume55
dc.description.issue6
dc.description.startingpage508
dc.description.endingpage512
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.gnosis.orcid0000-0002-2195-9961
dc.gnosis.orcid0000-0002-2106-1713


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record