Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/28637
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dc.contributor.authorGür, Serhat-
dc.contributor.authorÜnal, Bülent-
dc.contributor.authorÖzbek, Umut-
dc.contributor.authorÖzmen, Vahit-
dc.contributor.authorAydoğan, Fatih-
dc.contributor.authorGüllüoğlu, Bahadır Mahmut-
dc.contributor.authorAksaz, Erol-
dc.contributor.authorÖzbaş, Serdar Mustafa-
dc.contributor.authorBaşkan, Semih-
dc.contributor.authorKoyuncu, Ayhan-
dc.contributor.authorSoran, Atilla-
dc.date.accessioned2022-09-12T07:53:32Z-
dc.date.available2022-09-12T07:53:32Z-
dc.date.issued2010-01-
dc.identifier.citationGür, S. vd. (2010). "Validation of breast cancer nomograms for predicting the non-sentinel lymph node metastases after a positive sentinel lymph node biopsy in a multi-center study". European Journal of Surgical Oncology, 36(1), 30-35.en_US
dc.identifier.issn0748-7983-
dc.identifier.issn1532-2157-
dc.identifier.urihttps://doi.org/10.1016/j.ejso.2009.05.007-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0748798309001723-
dc.identifier.urihttp://hdl.handle.net/11452/28637-
dc.description.abstractObjective: In the study, our aim was to evaluate the predictability of four different nomograms on non-sentinel lymph node metastases (NSLNM) in breast cancer (BC) patients with positive sentinel lymph node (SLN) biopsy in a multi-center study. Methods: We identified 607 patients who had a positive SLN biopsy and completion axillary lymph node dissection (CALND) at seven different BC treatment centers in Turkey. The BC nomograms developed by the Memorial Sloan Kettering Cancer Center (MSKCC), Tenon Hospital, Cambridge University, and Stanford University were used to calculate the probability of NSLNM. Area under (AUC) Receiver Operating Characteristics Curve (ROC) was calculated for each nomogram and values greater than 0.70 were accepted as demonstrating good discrimination. Results: Two hundred and eighty-seven patients (287) of 607 patients (47.2%) had a positive axillary NSLNM. The AUC values were 0.705, 0.711, 0.730, and 0.582 for the MSKCC, Cambridge, Stanford, and Tenon models, respectively. On the multivariate analysis; overall metastasis size (OMS), lymphovascular invasion (LVI), and proportion of positive SLN to total SLN were found statistically significant. We created a formula to predict the NSLNM in our patient population and the AUC value of this formula was 0.8023. Conclusions: The MSKCC, Cambridge, and Stanford nomograms were good discriminators of NSLNM in SLN positive BC patients in this study. A newly created formula in this Study needs to be validated in prospective studies in different patient populations. A nomogram to predict NSLNM in patients with positive SLN biopsy developed at one institution should be used with caution.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBreast canceren_US
dc.subjectSentinel lymph nodeen_US
dc.subjectNon-sentinel lymph nodeen_US
dc.subjectNomogramen_US
dc.subjectLikelihooden_US
dc.subjectInvolvementen_US
dc.subjectCarcinomaen_US
dc.subjectDissectionen_US
dc.subjectLimitationsen_US
dc.subjectModelsen_US
dc.subjectOncologyen_US
dc.subjectSurgeryen_US
dc.subject.meshAdulten_US
dc.subject.meshAgeden_US
dc.subject.meshAged, 80 and overen_US
dc.subject.meshArea under curveen_US
dc.subject.meshAxillaen_US
dc.subject.meshBreast neoplasmsen_US
dc.subject.meshFemaleen_US
dc.subject.meshHumansen_US
dc.subject.meshLymph node excisionen_US
dc.subject.meshLymphatic metastasisen_US
dc.subject.meshMiddle ageden_US
dc.subject.meshModels, statisticalen_US
dc.subject.meshNeoplasm stagingen_US
dc.subject.meshNomogramsen_US
dc.subject.meshSensitivity and specificityen_US
dc.subject.meshSentinel lymph node biopsyen_US
dc.titleValidation of breast cancer nomograms for predicting the non-sentinel lymph node metastases after a positive sentinel lymph node biopsy in a multi-center studyen_US
dc.typeArticleen_US
dc.identifier.wos000274672100005tr_TR
dc.identifier.scopus2-s2.0-73249118710tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Genel Cerrahi Anabilim Dalı.tr_TR
dc.identifier.startpage30tr_TR
dc.identifier.endpage35tr_TR
dc.identifier.volume36tr_TR
dc.identifier.issue1tr_TR
dc.relation.journalEuropean Journal of Surgical Oncologyen_US
dc.contributor.buuauthorGökgöz, Şehsuvar-
dc.relation.collaborationYurt içitr_TR
dc.relation.collaborationYurt dışıtr_TR
dc.relation.collaborationSanayitr_TR
dc.identifier.pubmed19535217tr_TR
dc.subject.wosOncologyen_US
dc.subject.wosSurgeryen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ2 (Oncology)en_US
dc.wos.quartileQ1 (Surgery)en_US
dc.contributor.scopusid6603238737tr_TR
dc.subject.scopusBreast Neoplasms; Lymphoscintigraphy; Micrometastasisen_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeAgeden_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeAxillary lymph nodeen_US
dc.subject.emtreeBreast canceren_US
dc.subject.emtreeCancer centeren_US
dc.subject.emtreeCancer invasionen_US
dc.subject.emtreeCancer patienten_US
dc.subject.emtreeClinical trialen_US
dc.subject.emtreeDiagnostic valueen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHuman tissueen_US
dc.subject.emtreeLymph node dissectionen_US
dc.subject.emtreeLymph node metastasisen_US
dc.subject.emtreeMajor clinical studyen_US
dc.subject.emtreeMulticenter studyen_US
dc.subject.emtreeNomogramen_US
dc.subject.emtreePatient identificationen_US
dc.subject.emtreePriority journalen_US
dc.subject.emtreeSentinel lymph node biopsyen_US
dc.subject.emtreeTurkey (bird)en_US
dc.subject.emtreeValidation studyen_US
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