Efficacy of subsequent treatments in patients with hormone-positive advanced breast cancer who had disease progression under CDK 4/6 inhibitor therapy

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Özet

Background: 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).

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/11732Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1186/s12885-023-10609-8Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorKaracin, Cengiz
dc.contributor.authorOksuzoglu, Berna
dc.contributor.authorDemirci, Ayşe
dc.contributor.authorKeskinkılıç, Merve
dc.contributor.authorBaytemür, Naziyet Köse
dc.contributor.authorYılmaz, Funda
dc.contributor.authorSelvi, Oğuzhan
dc.contributor.authorErdem, Dilek
dc.contributor.authorAvşar, Esin
dc.contributor.authorPaksoy, Nail
dc.contributor.authorDemir, Necla
dc.contributor.authorGöksu, Sema Sezgin
dc.contributor.authorTürker, Sema
dc.contributor.authorBayram, Ertuğrul
dc.contributor.authorÇelebi, Abdüssamet
dc.contributor.authorYılmaz, Hatice
dc.contributor.authorKuzu, Ömer Faruk
dc.contributor.authorKahraman, Seda
dc.contributor.authorGökmen, İvo
dc.contributor.authorSakin, Abdullah
dc.contributor.authorAlkan, Ali
dc.contributor.authorNayır, Erdinç
dc.contributor.authorUğraklı, Muzaffer
dc.contributor.authorAcar, Ömer
dc.contributor.authorErtürk, İsmail
dc.contributor.authorDemir, Hacer
dc.contributor.authorAslan, Ferit
dc.contributor.authorSönmez, Özlem
dc.contributor.authorKorkmaz, Taner
dc.contributor.authorCelayir, Özde Melisa
dc.contributor.authorKaradağ, İbrahim
dc.contributor.authorKayıkçıoğlu, Erkan
dc.contributor.authorŞakalar, Teoman
dc.contributor.authorÖktem, İlker Nihat
dc.contributor.authorEren, Tülay
dc.contributor.authorUrul, Enes
dc.contributor.authorMocan, Eda Eylemer
dc.contributor.authorKalkan, Ziya
dc.contributor.authorYıldırım, Nilgün
dc.contributor.authorErgün, Yakup
dc.contributor.authorAkagündüz, Baran
dc.contributor.authorKarakaya, Serdar
dc.contributor.authorKut, Engin
dc.contributor.authorTeker, Fatih
dc.contributor.authorDemirel, Burçin Çakan
dc.contributor.authorKaraboyun, Kubilay
dc.contributor.authorAlmuradova, Elvina
dc.contributor.authorÜnal, Olçun Ümit
dc.contributor.authorOyman, Abdilkerim
dc.contributor.authorIşık, Deniz
dc.date.accessioned2026-10-18T20:26:44.205650111Z
dc.date.available2026-10-18T20:26:44.205650111Z
dc.date.issued2023
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).
dc.description.sponsorshipSpecial thanks to Turkish Oncology Group (TOG) - Breast Cancer Consortium.
dc.identifier.doi10.1186/s12885-023-10609-8
dc.identifier.issn1471-2407
dc.identifier.issue1
dc.identifier.pmcidPMC9912535
dc.identifier.pmid36765293
dc.identifier.scopus2-s2.0-85147894207
dc.identifier.startpage136
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/11732
dc.identifier.volume23
dc.language.isoen
dc.publisherBioMed Central Ltd
dc.relation.ispartofBMC Cancer
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAdvanced breast cancer
dc.subjectCyclin-dependent kinase
dc.subjectEndocrine treatment
dc.subjectEverolimus
dc.subjectFulvestrant
dc.subjectHormonotherapy
dc.subjectPalbociclib
dc.subjectRibociclib
dc.subjectAntineoplastic Combined Chemotherapy Protocols
dc.subjectBreast Neoplasms
dc.subjectDisease Progression
dc.subjectFemale
dc.subjectHumans
dc.subjectProtein Kinase Inhibitors
dc.subjectReceptor, ErbB-2
dc.subjectcyclin dependent kinase 4
dc.subjectcyclin dependent kinase 6
dc.subjectcyclin dependent kinase inhibitor
dc.subjectmammalian target of rapamycin
dc.subjectantineoplastic agent
dc.subjectepidermal growth factor receptor 2
dc.subjectprotein kinase inhibitor
dc.subjectadult
dc.subjectaged
dc.subjectArticle
dc.subjectcancer chemotherapy
dc.subjectcancer combination chemotherapy
dc.subjectcancer growth
dc.subjectcancer therapy
dc.subjectcontrolled study
dc.titleEfficacy of subsequent treatments in patients with hormone-positive advanced breast cancer who had disease progression under CDK 4/6 inhibitor therapy
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus23
rdl.departmentDepartment of Medical Oncology, Erzincan Binali Yıldırım University, Erzincan, Turkey.
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexPUBMED