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The efficacy of two different dosages of epirubicin in neoadjuvant setting: FEC50 v.s. FEC100. Preliminary report

dc.contributor.authorDemiray, M.
dc.contributor.authorEvrensel, T.
dc.contributor.authorKanat, O.
dc.contributor.authorKurt, E.
dc.contributor.authorArslan, M.
dc.contributor.authorSaraydaroǧlu, O.
dc.contributor.authorErcan, I.
dc.contributor.authorGönüllü, G.
dc.contributor.authorGökgöz, S.
dc.contributor.authorTolunay, S.
dc.contributor.authorGözkaman, A.
dc.contributor.authorAkgül, N.
dc.contributor.authorTaşdelen, I.
dc.contributor.authorManavoǧlu, O.
dc.contributor.buuauthorDemiray, Mutlu
dc.contributor.buuauthorEVRENSEL, TÜRKKAN
dc.contributor.buuauthorKanat, Ozkän
dc.contributor.buuauthorARSLAN, MURAT
dc.contributor.buuauthorSARAYDAROĞLU, ÖZLEM
dc.contributor.buuauthorERCAN, İLKER
dc.contributor.buuauthorGönüllü, Güzin
dc.contributor.buuauthorGÖKGÖZ, MUSTAFA ŞEHSUVAR
dc.contributor.buuauthorTOLUNAY, ŞAHSİNE
dc.contributor.department Tıp Fakültesi
dc.contributor.departmentTıbbi Onkoloji Ana Bilim Dalı
dc.contributor.orcid0009-0000-6166-4466
dc.contributor.orcid0000-0002-2382-290X
dc.contributor.orcid0000-0002-5771-7649
dc.contributor.scopusid 6603631569
dc.contributor.scopusid6603942124
dc.contributor.scopusid55881548500
dc.contributor.scopusid7006207332
dc.contributor.scopusid57197925370
dc.contributor.scopusid15074395500
dc.contributor.scopusid6603789069
dc.contributor.scopusid6506410014
dc.contributor.scopusid6603238737
dc.contributor.scopusid6602604390
dc.date.accessioned2025-08-06T23:58:09Z
dc.date.issued2005-12-07
dc.description.abstractNeoadjuvant chemotherapy is increasingly used in the treatment of patients with large tumor and locally advanced breast cancer. We evaluated the efficacy of FEC50 (5-fluorouracil 500 mg/m<sup>2</sup>, epirubicin 50 mg/m<sup>2</sup>, cyclophosphamide 500 mg/m<sup>2</sup>) and FEC100 (same regimen except with epirubicin 100 mg/m<sup>2</sup>) chemotherapy regimen in neoadjuvant setting. Fifty-one eligible patients with stage II-III invasive breast carcinoma were retrospectively analyzed. FEC50 group included 25, FEC100 group included 26 patients. Mammographic and ultrasonographic determination of tumor size and nodal status at the initial and preoperative stages were considered to evaluate the efficacy of chemotherapy. Both groups were to receive median 4 (3-4) cycle chemotherapy. Pretreatment features of the patients and tumors were similar in both groups. The response rate was 48% (95% CI, 28.4-67.5) in FEC50, and 57.6% (95% CI, 38.4-76.5) in FEC100 group. Clinical and pathological complete response rate was 4% (95% CI, 0.0-11.6) in FEC50, and 15.3% (95% CI, 1.4-29.1), 7.6% (95% CI, 0.0-17.7) in FEC100. In this retrospective analysis of our own experience, the response rates observed in FEC50 and FEC100 groups are similar after 4 cycles of neoadjuvant chemotherapy.
dc.identifier.endpage25
dc.identifier.issn1019-3103
dc.identifier.issue1
dc.identifier.scopus2-s2.0-28244483859
dc.identifier.startpage19
dc.identifier.urihttps://hdl.handle.net/11452/54221
dc.identifier.volume35
dc.indexed.scopusScopus
dc.language.isoen
dc.relation.journalTurkish Journal of Cancer
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectNeoadjuvant chemotherapy
dc.subjectEpirubicin
dc.titleThe efficacy of two different dosages of epirubicin in neoadjuvant setting: FEC50 v.s. FEC100. Preliminary report
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Tıbbi Onkoloji Ana Bilim Dalı
local.indexed.atScopus
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relation.isAuthorOfPublication11cb580f-980e-4dde-92c5-66e7ea4cddaf
relation.isAuthorOfPublication50e4dfdb-25cd-43af-94c9-464881669605
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relation.isAuthorOfPublication.latestForDiscoveryeceff514-6af7-4c3b-a146-b77546565a6c

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