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dc.contributor.authorBilici, Ahmet
dc.contributor.authorUysal, Mükremin
dc.contributor.authorMenekşe, Serkan
dc.contributor.authorAkın, Semih
dc.contributor.authorYıldız, Fatih
dc.contributor.authorTuran, Merve
dc.contributor.authorSezgin Göksu, Sema
dc.contributor.authorBeypınar, İsmail
dc.contributor.authorSakalar, Teoman
dc.contributor.authorDeğirmenci, Mustafa
dc.contributor.authorErdem, Dilek
dc.contributor.authorBaşaran, Gül
dc.contributor.authorÖlmez, Ömer Fatih
dc.contributor.authorAvcı, Nilüfer
dc.contributor.authorTural, Deniz
dc.contributor.authorSakin, Abdullah
dc.contributor.authorTürker, Sema
dc.contributor.authorDemir, Atakan
dc.contributor.authorTemiz, Süleyman
dc.contributor.authorKaplan, Muhammed Ali
dc.contributor.authorDoğan, Mutlu
dc.contributor.authorTanrıverdi, Özgür
dc.contributor.authorBilgetekin, İrem
dc.contributor.authorYeşil Çınkır, Havva
dc.contributor.authorAçıkgöz, Özgür
dc.contributor.authorPaydaş, Semra
dc.contributor.authorUslu, Rüçhan
dc.contributor.authorTurhal, Serdar
dc.date.accessioned2023-01-10T13:00:49Z
dc.date.available2023-01-10T13:00:49Z
dc.date.issued2022en_US
dc.identifier.citationBilici, A., Uysal, M., Menekşe, S., Akın, S., Yıldız, F., Turan, M. ... Turhal, S. (2022). Real-life analysis of efficacy and safety of everolimus plus exemestane in hormone receptor-positive, human epidermal growth factor receptor-2-negative metastatic breast cancer patients: A Turkish Oncology Group (TOG) study. Cancer Investigation, 40(2), 199-209. https://dx.doi.org/10.1080/07357907.2021.2017952en_US
dc.identifier.issn0735-7907
dc.identifier.issn1532-4192
dc.identifier.urihttps://dx.doi.org/10.1080/07357907.2021.2017952
dc.identifier.urihttps://hdl.handle.net/20.500.12511/10281
dc.description.abstractPurpose: This study evaluated the efficacy and safety of everolimus (EVE) plus exemestane (EXE) in hormone-receptor positive (HR+), human epidermal growth factor receptor-2-negative (HER2−) metastatic breast cancer (MBC) patients in real-life settings. Methods: Overall, 204 HR+, HER2− MBC patients treated with EVE + EXE after progressing following prior endocrine treatment were included. Overall survival (OS) and progression-free survival (PFS) and safety data were analyzed. Results: The objective response rate, median PFS, and median OS were 33.4%, 8.9 months, and 23.4 months, respectively. Multivariate analysis revealed that negative progesterone receptor status was a significant determinant of poor treatment response (p = 0.035) and PFS (p = 0.024). The presence of bone-only metastasis was associated with better treatment response (p = 0.002), PFS (p < 0.001), and OS (p = 0.001). Conclusion: We confirmed the favorable efficacy and safety profile of EVE + EXE for HR+, HER − MBC patients.en_US
dc.language.isoengen_US
dc.publisherTaylor & Francis Incen_US
dc.rightsinfo:eu-repo/semantics/embargoedAccessen_US
dc.subjectEverolimusen_US
dc.subjectExemestaneen_US
dc.subjectMetastatic Breast Canceren_US
dc.subjectHormone Receptor-Positiveen_US
dc.subjectHER Negativeen_US
dc.subjectEfficacyen_US
dc.titleReal-life analysis of efficacy and safety of everolimus plus exemestane in hormone receptor-positive, human epidermal growth factor receptor-2-negative metastatic breast cancer patients: A Turkish Oncology Group (TOG) studyen_US
dc.typearticleen_US
dc.relation.ispartofCancer Investigationen_US
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, İç Hastalıkları Ana Bilim Dalıen_US
dc.authorid0000-0002-0443-6966en_US
dc.authorid0000-0001-7934-7039en_US
dc.authorid0000-0003-2715-4002en_US
dc.identifier.volume40en_US
dc.identifier.issue2en_US
dc.identifier.startpage199en_US
dc.identifier.endpage209en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1080/07357907.2021.2017952en_US
dc.institutionauthorBilici, Ahmet
dc.institutionauthorÖlmez, Ömer Fatih
dc.institutionauthorAçıkgöz, Özgür
dc.identifier.wosqualityQ4en_US
dc.identifier.wos000734258300001en_US
dc.identifier.scopus2-s2.0-85121803055en_US
dc.identifier.pmid34894960en_US
dc.identifier.scopusqualityQ2en_US


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