Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/7847
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dc.contributor.authorGumusay, O.-
dc.contributor.authorCoskun, U.-
dc.contributor.authorAkman, T.-
dc.contributor.authorEkinci, A.S.-
dc.contributor.authorKocar, M.-
dc.contributor.authorErceleb, O.B.-
dc.contributor.authorYazici, O.-
dc.date.accessioned2019-08-16T12:32:47Z
dc.date.available2019-08-16T12:32:47Z
dc.date.issued2014-
dc.identifier.issn0171-5216-
dc.identifier.urihttps://hdl.handle.net/11499/7847-
dc.identifier.urihttps://doi.org/10.1007/s00432-013-1553-7-
dc.description.abstractBackground: The development of brain metastases (BMs) was associated with poor prognosis in melanoma patients. Patients with BMs have a median survival of <6 months. Melanoma is the third most common tumor to metastasize to the brain with a reported incidence of 10-40 %. Our aim was to identify factors predicting development of BMs and survival. Patients and methods: We performed a retrospective analysis of 470 melanoma patients between 2000 and 2012. The logistic regression analyses were used to identify the clinicopathological features of primary melanoma that are predictive of BMs development and survival after a diagnosis of brain metastases. Results: There were 52 patients (11.1 %) who developed melanoma BMs during the study period. The analysis of post-BMs with Kaplan-Meier curves has resulted in a median survival rate of 4.1 months (range 2.9-5.1 months). On logistic regression analysis site of the primary tumor on the head and neck (p = 0.002), primary tumor thickness (Breslow >4 mm) (p = 0.008), ulceration (p = 0.007), and pathologically N2 and N3 diseases (p = 0.001) were found to be significantly associated with the development of BMs. In univariate analysis, tumor thickness and performance status had a significant influence on post-BMs survival. In multivariate analysis, these clinicopathologic factors were not remained as significant predictive factors. Conclusions: Our results revealed the importance of primary tumor characteristics associated with the development of BMs. Ulceration, primary tumor thickness, anatomic site, and pathologic ?N2 disease were found to be significant predictors of BMs development. © 2013 Springer-Verlag Berlin Heidelberg.en_US
dc.language.isoenen_US
dc.relation.ispartofJournal of Cancer Research and Clinical Oncologyen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBrain metastasesen_US
dc.subjectMelanomaen_US
dc.subjectPredictive factorsen_US
dc.subjectadulten_US
dc.subjectageden_US
dc.subjectarticleen_US
dc.subjectbrain metastasisen_US
dc.subjectcancer sizeen_US
dc.subjectcancer stagingen_US
dc.subjectcancer survivalen_US
dc.subjectclinical featureen_US
dc.subjectcontrolled studyen_US
dc.subjectfemaleen_US
dc.subjecthumanen_US
dc.subjectmajor clinical studyen_US
dc.subjectmaleen_US
dc.subjectmelanomaen_US
dc.subjectmiddle ageden_US
dc.subjectpredictive valueen_US
dc.subjectprimary tumoren_US
dc.subjectpriority journalen_US
dc.subjectretrospective studyen_US
dc.subjectsurvival rateen_US
dc.subjectsurvival timeen_US
dc.subjecttumor localizationen_US
dc.subjectulceren_US
dc.subjectvery elderlyen_US
dc.subjectyoung adulten_US
dc.titlePredictive factors for the development of brain metastases in patients with malignant melanoma: A study by the Anatolian society of medical oncologyen_US
dc.typeArticleen_US
dc.identifier.volume140en_US
dc.identifier.issue1en_US
dc.identifier.startpage151
dc.identifier.startpage151en_US
dc.identifier.endpage157en_US
dc.authorid0000-0003-4755-2753-
dc.identifier.doi10.1007/s00432-013-1553-7-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid24292400en_US
dc.identifier.scopus2-s2.0-84892670407en_US
dc.identifier.wosWOS:000329236800017en_US
dc.identifier.scopusqualityQ1-
dc.ownerPamukkale University-
item.languageiso639-1en-
item.openairetypeArticle-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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