Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/34180
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dc.contributor.authorUlaş, Arife-
dc.date.accessioned2023-10-02T10:48:45Z-
dc.date.available2023-10-02T10:48:45Z-
dc.date.issued2015-01-01-
dc.identifier.citationAvci, N. vd. (2015). "Neoadjuvant chemotherapy-induced changes in immunohistochemical expression of estrogen receptor, progesterone receptor, HER2, and Ki-67 in patients with breast cancer". Journal of B.U.ON., 20(1), 45-49.en_US
dc.identifier.issn1107-0625-
dc.identifier.urihttps://doi.org/-
dc.identifier.urihttp://hdl.handle.net/11452/34180-
dc.description.abstractPurpose: The impact of neoadjuvant chemotherapy (NACT) on immunohistochemical markers in breast cancer specimens remains controversial. We designed the current study to investigate the potential changes in estrogen receptor (ER), progesterone receptor (PR), HER2, and Ki-67 expression before and after NACT in a cohort of Turkish patients with breast cancer. Methods: This research was designed as a prospective, observational study of 100 consecutive patients with breast cancer (mean age 47.8 11.4 years) who were scheduled to undergo anthracycline- and/or taxane-containing NACT before attempting cytoreductive surgery at the Department of Oncology of the Uludag University Medical Center, Bursa, Turkey. Immunohistochemistry was performed on formalin-fixed, paraffin-embedded specimens. Results: Changes in immunohistochemical markers before and after NACT were only significant for HER-2 and Ki-67. More specifically, the number of HER-2-positive specimens decreased front 21 before NACT to 8 after NACT (p<0.001). Similarly, the number of tumor samples positive for Ki-67 decreased significantly from 65 to 24 after NACT (p<0.001). Mean pre- and post-treatment tumor grades of differentiation before and after NACT were 2.56 +/- 0.67 and 2.37 +/- 1.07, respectively (p<0.05). We did not find any significant associations between baseline ER, PR, HER2, and Ki-67 expression with both overall survival (OS) and disease-free survival (DFS). Conclusion: Our study suggests that NACT reduces the expression of HER2 and Ki-67 in breast cancer specimens. The significance of NACT-induced changes in the immunohistochemical expression of HER2 and Ki-67 in patients with breast cancer should be further studied in future translational and clinical research.en_US
dc.language.isoenen_US
dc.publisherImprimatur Publicationsen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBreast canceren_US
dc.subjectEstrogen/progesterone receptoren_US
dc.subjectHER2en_US
dc.subjectImmunohistochemistryen_US
dc.subjectKi-67en_US
dc.subjectNeoadjuvant chemotherapyen_US
dc.subjectKI67en_US
dc.subjectOncologyen_US
dc.subject.meshAdulten_US
dc.subject.meshAnthracyclinesen_US
dc.subject.meshAntineoplastic combined chemotherapy protocolsen_US
dc.subject.meshBreast neoplasmsen_US
dc.subject.meshChemotherapy, adjuvanten_US
dc.subject.meshDisease-Free survivalen_US
dc.subject.meshFemaleen_US
dc.subject.meshHumansen_US
dc.subject.meshImmunohistochemistryen_US
dc.subject.meshKi-67 antigenen_US
dc.subject.meshMiddle ageden_US
dc.subject.meshNeoadjuvant therapyen_US
dc.subject.meshNeoplasm gradingen_US
dc.subject.meshPredictive value of testsen_US
dc.subject.meshProspective studiesen_US
dc.subject.meshReceptor, ErbB-2en_US
dc.subject.meshReceptors, estrogenen_US
dc.subject.meshReceptors, progesteroneen_US
dc.subject.meshSurvival analysisen_US
dc.subject.meshTaxoidsen_US
dc.subject.meshTime factorsen_US
dc.subject.meshTreatment outcomeen_US
dc.subject.meshTurkeyen_US
dc.titleNeoadjuvant chemotherapy-induced changes in immunohistochemical expression of estrogen receptor, progesterone receptor, HER2, and Ki-67 in patients with breast canceren_US
dc.typeArticleen_US
dc.identifier.wos000351566500007tr_TR
dc.identifier.scopus2-s2.0-84928700466tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/İç Hastalıkları Anabilim Dalı/Tıbbi Onkoloji Bilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Tıbbi Patoloji Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Genel Cerrahi Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0003-1094-5772tr_TR
dc.contributor.orcid0000-0002-3669-6391tr_TR
dc.contributor.orcid0000-0002-9038-0515tr_TR
dc.contributor.orcid0000-0002-0070-0889tr_TR
dc.contributor.orcid0000-0001-7934-7039tr_TR
dc.contributor.orcid0000-0002-5446-1254tr_TR
dc.contributor.orcid0000-0002-9732-5340tr_TR
dc.identifier.startpage45tr_TR
dc.identifier.endpage49tr_TR
dc.identifier.volume20tr_TR
dc.identifier.issue1tr_TR
dc.relation.journalJournal of B.U.ON.en_US
dc.contributor.buuauthorAvci, Nilufer-
dc.contributor.buuauthorDeligonul, Adem-
dc.contributor.buuauthorTolunay, Sahsine-
dc.contributor.buuauthorCubukcu, Erdem-
dc.contributor.buuauthorOlmez, Omer Fatih-
dc.contributor.buuauthorHartavi, Mustafa-
dc.contributor.buuauthorKurt, Ender-
dc.contributor.buuauthorEvrensel, Turkkan-
dc.contributor.researcheridCCT-7946-2022tr_TR
dc.contributor.researcheridESM-4544-2022tr_TR
dc.contributor.researcheridAAI-1612-2021tr_TR
dc.contributor.researcheridETP-1691-2022tr_TR
dc.contributor.researcheridDJG-4827-2022tr_TR
dc.contributor.researcheridCUI-5353-2022tr_TR
dc.contributor.researcheridDAS-3088-2022tr_TR
dc.contributor.researcheridAAJ-1027-2021tr_TR
dc.relation.collaborationYurt içitr_TR
dc.relation.collaborationSanayitr_TR
dc.identifier.pubmed25778295tr_TR
dc.subject.wosOncologyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.contributor.scopusid55390409800tr_TR
dc.contributor.scopusid37088030300tr_TR
dc.contributor.scopusid6602604390tr_TR
dc.contributor.scopusid53986153800tr_TR
dc.contributor.scopusid26435400000tr_TR
dc.contributor.scopusid55370753300tr_TR
dc.contributor.scopusid7006207332tr_TR
dc.contributor.scopusid6603942124tr_TR
dc.subject.scopusNeoadjuvant therapy; Sentinel lymph node biopsy; Breast neoplasmsen_US
dc.subject.emtreeAnthracyclineen_US
dc.subject.emtreeEpidermal growth factor receptor 2en_US
dc.subject.emtreeEstrogen receptoren_US
dc.subject.emtreeKi 67 antigenen_US
dc.subject.emtreeProgesterone receptoren_US
dc.subject.emtreeTaxane derivativeen_US
dc.subject.emtreeAnthracyclineen_US
dc.subject.emtreeAntineoplastic agenten_US
dc.subject.emtreeEpidermal growth factor receptor 2en_US
dc.subject.emtreeERBB2 protein, humanen_US
dc.subject.emtreeEstrogen receptoren_US
dc.subject.emtreeKi 67 antigenen_US
dc.subject.emtreeProgesterone receptoren_US
dc.subject.emtreeTaxoiden_US
dc.subject.emtreeAdjuvant chemotherapyen_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeBreast canceren_US
dc.subject.emtreeBreast carcinomaen_US
dc.subject.emtreeClinical researchen_US
dc.subject.emtreeCytoreductive surgeryen_US
dc.subject.emtreeDisease free survivalen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHuman tissueen_US
dc.subject.emtreeImmunohistochemistryen_US
dc.subject.emtreeMajor clinical studyen_US
dc.subject.emtreeObservational studyen_US
dc.subject.emtreeOverall survivalen_US
dc.subject.emtreePostmenopauseen_US
dc.subject.emtreeProtein expressionen_US
dc.subject.emtreeAdjuvant chemotherapyen_US
dc.subject.emtreeAdjuvant therapyen_US
dc.subject.emtreeBreast neoplasmsen_US
dc.subject.emtreeCancer gradingen_US
dc.subject.emtreeMetabolismen_US
dc.subject.emtreeMiddle ageden_US
dc.subject.emtreeMortalityen_US
dc.subject.emtreePathologyen_US
dc.subject.emtreePredictive valueen_US
dc.subject.emtreeProspective studyen_US
dc.subject.emtreeSurvivalen_US
dc.subject.emtreeTimeen_US
dc.subject.emtreeTreatment outcomeen_US
dc.subject.emtreeTurkeyen_US
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