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dc.contributor.authorKaraçın, Cengiz
dc.contributor.authorÖksüzoğlu, Berna
dc.contributor.authorDemirci, Ayşe
dc.contributor.authorKeskinkılıç, Merve
dc.contributor.authorBaytemur, Naziyet Köse
dc.contributor.authorYılmaz, Funda
dc.contributor.authorSelvi, Oğuzhan
dc.contributor.authorKaraboyun, Kubilay
dc.date.accessioned2023-05-06T17:23:34Z
dc.date.available2023-05-06T17:23:34Z
dc.date.issued2023
dc.identifier.issn1471-2407
dc.identifier.urihttps://doi.org/10.1186/s12885-023-10609-8
dc.identifier.urihttps://hdl.handle.net/20.500.11776/12161
dc.description.abstractBackground: There is no standard treatment recommended at category 1 level in international guidelines for subsequent therapy after cyclin-dependent kinase 4/6 inhibitor (CDK4/6) based therapy. We aimed to evaluate which subsequent treatment oncologists prefer in patients with disease progression under CDKi. In addition, we aimed to show the effectiveness of systemic treatments after CDKi and whether there is a survival difference between hormonal treatments (monotherapy vs. mTOR-based). Methods: A total of 609 patients from 53 centers were included in the study. Progression-free-survivals (PFS) of subsequent treatments (chemotherapy (CT, n:434) or endocrine therapy (ET, n:175)) after CDKi were calculated. Patients were evaluated in three groups as those who received CDKi in first-line (group A, n:202), second-line (group B, n: 153) and ? 3rd-line (group C, n: 254). PFS was compared according to the use of ET and CT. In addition, ET was compared as monotherapy versus everolimus-based combination therapy. Results: The median duration of CDKi in the ET arms of Group A, B, and C was 17.0, 11.0, and 8.5 months in respectively; it was 9.0, 7.0, and 5.0 months in the CT arm. Median PFS after CDKi was 9.5 (5.0–14.0) months in the ET arm of group A, and 5.3 (3.9–6.8) months in the CT arm (p = 0.073). It was 6.7 (5.8–7.7) months in the ET arm of group B, and 5.7 (4.6–6.7) months in the CT arm (p = 0.311). It was 5.3 (2.5–8.0) months in the ET arm of group C and 4.0 (3.5–4.6) months in the CT arm (p = 0.434). Patients who received ET after CDKi were compared as those who received everolimus-based combination therapy versus those who received monotherapy ET: the median PFS in group A, B, and C was 11.0 vs. 5.9 (p = 0.047), 6.7 vs. 5.0 (p = 0.164), 6.7 vs. 3.9 (p = 0.763) months. Conclusion: Physicians preferred CT rather than ET in patients with early progression under CDKi. It has been shown that subsequent ET after CDKi can be as effective as CT. It was also observed that better PFS could be achieved with the subsequent everolimus-based treatments after first-line CDKi compared to monotherapy ET. © 2023, The Author(s).en_US
dc.description.sponsorshipSpecial thanks to Turkish Oncology Group (TOG) - Breast Cancer Consortium.en_US
dc.language.isoengen_US
dc.publisherBioMed Central Ltden_US
dc.identifier.doi10.1186/s12885-023-10609-8
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAdvanced breast canceren_US
dc.subjectCyclin-dependent kinaseen_US
dc.subjectEndocrine treatmenten_US
dc.subjectEverolimusen_US
dc.subjectFulvestranten_US
dc.subjectHormonotherapyen_US
dc.subjectPalbocicliben_US
dc.subjectRibocicliben_US
dc.subjectcyclin dependent kinase 4en_US
dc.subjectcyclin dependent kinase 6en_US
dc.subjectcyclin dependent kinase inhibitoren_US
dc.subjecteverolimusen_US
dc.subjectfulvestranten_US
dc.subjectmammalian target of rapamycinen_US
dc.subjectpalbocicliben_US
dc.subjectribocicliben_US
dc.subjectantineoplastic agenten_US
dc.subjectepidermal growth factor receptor 2en_US
dc.subjecteverolimusen_US
dc.subjectprotein kinase inhibitoren_US
dc.subjectadulten_US
dc.subjectadvanced breast canceren_US
dc.subjectageden_US
dc.subjectArticleen_US
dc.subjectcancer chemotherapyen_US
dc.subjectcancer combination chemotherapyen_US
dc.subjectcancer growthen_US
dc.subjectcancer therapyen_US
dc.subjectcontrolled studyen_US
dc.subjectdrug efficacyen_US
dc.subjectdrug useen_US
dc.subjecthormonal therapyen_US
dc.subjecthumanen_US
dc.subjectmajor clinical studyen_US
dc.subjectmonotherapyen_US
dc.subjectpatient careen_US
dc.subjectphysicianen_US
dc.subjectprogression free survivalen_US
dc.subjectretrospective studyen_US
dc.subjectsurvival analysisen_US
dc.subjecttreatment durationen_US
dc.subjectbreast tumoren_US
dc.subjectdisease exacerbationen_US
dc.subjectfemaleen_US
dc.subjectAntineoplastic Combined Chemotherapy Protocolsen_US
dc.subjectBreast Neoplasmsen_US
dc.subjectDisease Progressionen_US
dc.subjectEverolimusen_US
dc.subjectFemaleen_US
dc.subjectFulvestranten_US
dc.subjectHumansen_US
dc.subjectProtein Kinase Inhibitorsen_US
dc.subjectReceptor, ErbB-2en_US
dc.titleEfficacy of subsequent treatments in patients with hormone-positive advanced breast cancer who had disease progression under CDK 4/6 inhibitor therapyen_US
dc.typearticleen_US
dc.relation.ispartofBMC Canceren_US
dc.departmentFakülteler, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Radyasyon Onkolojisi Ana Bilim Dalıen_US
dc.identifier.volume23en_US
dc.identifier.issue1en_US
dc.institutionauthorKaraboyun, Kubilay
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid57211313828
dc.authorscopusid6701488999
dc.authorscopusid55754179900
dc.authorscopusid57801244000
dc.authorscopusid57224538924
dc.authorscopusid58100171900
dc.authorscopusid57348194400
dc.identifier.scopus2-s2.0-85147894207en_US
dc.identifier.pmid36765293en_US


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