Show simple item record

dc.contributor.authorFountzilas, Georgeen
dc.contributor.authorSkarlos, Dimosthenis V.en
dc.contributor.authorGiannakakis, T.en
dc.contributor.authorAthanasiades, A.en
dc.contributor.authorBafaloukos, Dimitriosen
dc.contributor.authorKalogera-Fountzila, Annaen
dc.contributor.authorBamia, C.en
dc.contributor.authorPavlidis, Nicholasen
dc.contributor.authorKosmidis, Paraskevas A.en
dc.creatorFountzilas, Georgeen
dc.creatorSkarlos, Dimosthenis V.en
dc.creatorGiannakakis, T.en
dc.creatorAthanasiades, A.en
dc.creatorBafaloukos, Dimitriosen
dc.creatorKalogera-Fountzila, Annaen
dc.creatorBamia, C.en
dc.creatorPavlidis, Nicholasen
dc.creatorKosmidis, Paraskevas A.en
dc.date.accessioned2018-06-22T09:53:07Z
dc.date.available2018-06-22T09:53:07Z
dc.date.issued1994
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/41668
dc.description.abstract50 women with advanced breast cancer were treated with an intensified regimen which consisted of high-dose epirubicin (110 mg/m2) every 2 weeks and filgrastim (5 μg/kg) subcutaneously for 13 days, starting 24 h after chemotherapy. 44 patients completed all six cycles. The median interval between cycles of treatment was 14.3 days. The actually administered median dose per unit time per patient was 53 mg/m2/week, amounting to 97.2% of the dose prescribed by the protocol. 7 [14%, 95% confidence interval (C.I.) 4-24%] patients achieved a complete and 25 (50%, 95% C.I. 36-64%) a partial response. Median time to progression was 32 weeks and median survival 64 weeks. Stomatitis and fever each occurred in 7 (14%) patients. Grade 3 haematological toxicity was observed in 6 (12%) patients. 1 (2%) patient developed grade 4 cardiac toxicity. This intensified regimen appears to be a well tolerated and effective treatment in advanced breast cancer. © 1994.en
dc.language.isoengen
dc.sourceEuropean journal of canceren
dc.subjectArticleen
dc.subjectHumanen
dc.subjectAdulten
dc.subjectAgeden
dc.subjectBreast canceren
dc.subjectBreast neoplasmsen
dc.subjectFemaleen
dc.subjectAdvanced canceren
dc.subjectDisease progressionen
dc.subjectDrug responseen
dc.subjectPriority journalen
dc.subjectAntineoplastic combined chemotherapy protocolsen
dc.subjectClinical articleen
dc.subjectClinical trialen
dc.subjectGranulocyte colony-stimulating factoren
dc.subjectLocalen
dc.subjectNeoplasm recurrenceen
dc.subjectRecombinant granulocyte colony stimulating factoren
dc.subjectStomatitisen
dc.subjectTreatment outcomeen
dc.subjectCardiotoxicityen
dc.subjectFeveren
dc.subjectSurvivalen
dc.subjectTime factorsen
dc.subjectEpirubicinen
dc.subjectSubcutaneous drug administrationen
dc.subjectBlood toxicityen
dc.subjectMiddle ageen
dc.subjectPatient complianceen
dc.subjectFilgrastimen
dc.subjectGrowth factoren
dc.subjectIntensive chemotherapyen
dc.subjectRecombinant proteinsen
dc.titleIntensive chemotherapy with high-dose epirubicin every 2 weeks and prophylactic administration of filgrastim in advanced breast canceren
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/0959-8049(94)90124-4
dc.description.volume30
dc.description.issue7
dc.description.startingpage965
dc.description.endingpage969
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


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