Please use this identifier to cite or link to this item: https://repository.southwesthealthcare.com.au/swhealthcarejspui/handle/1/4410
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dc.contributor.authorWigston, Lucas-
dc.contributor.authorMorris, Ali-
dc.contributor.authorWen Lok, Sheau-
dc.contributor.authorBaron-Hay, Sally-
dc.contributor.authorde Boer, Richard-
dc.contributor.authorBoyle, Frances-
dc.contributor.authorCollins, Ian M.-
dc.contributor.authorCuff, Katharine-
dc.contributor.authorGately, Lucy-
dc.contributor.authorGeorgiou, Chloe-
dc.contributor.authorGreenberg, Sally-
dc.contributor.authorKarki, Bhaskar-
dc.contributor.authorMok, Kelly-
dc.contributor.authorMorton, Catherine-
dc.contributor.authorNottage, Michelle-
dc.contributor.authorRainey, Natalie-
dc.contributor.authorTorres, Javier-
dc.contributor.authorTung, Iris-
dc.contributor.authorWong, Vanessa-
dc.contributor.authorJude, Evon-
dc.contributor.authorGibbs, Peter-
dc.contributor.authorNott, Louise-
dc.date.accessioned2026-08-06T23:38:14Z-
dc.date.available2026-08-06T23:38:14Z-
dc.date.issued2026-07-30-
dc.identifier.issnOnline ISSN: 1445-5994en
dc.identifier.issnPrint ISSN: 1444-0903en
dc.identifier.urihttps://repository.southwesthealthcare.com.au/swhealthcarejspui/handle/1/4410-
dc.description.abstractBackground Hormone receptor-positive, HER2− breast cancer (HR+/HER2−) represents most advanced breast cancer (ABC) cases. Patients with visceral metastases are considered to have aggressive disease, historically treated with first-line chemotherapy (CT). However, trials (RIGHT Choice, PADMA, ABIGAIL) have demonstrated that cyclin-dependent kinase 4/6 inhibitors (CDK4/6i) combined with endocrine therapy (ET) provide superior efficacy and tolerability in this setting. Aims To compare outcomes between first-line CDK4/6i + ET and CT in Australian patients with HR+/HER2− ABC and visceral metastases. Methods Data were obtained from the ARORA registry, a prospective observational study capturing real-world outcomes for Australian patients with HR+/HER2− ABC. Eligible patients were aged ≥18 years, with visceral metastases diagnosed after 1 January 2020, and received first-line systemic therapy. Participants were stratified by initial treatment: CT, ET + CDK4/6i or ET monotherapy. ET monotherapy was analysed as a separate cohort and excluded from comparative progression-free survival (PFS) and overall survival (OS) analyses. Primary endpoints were (1) OS: time from metastatic diagnosis to death and (2) PFS: time to progression on first-line therapy. Results A total of 418 patients were included, with a median age of 56 years and median follow-up of 12 months. The majority of patients (73.7%) received first-line CDK4/6i + ET. Compared with CT, CDK4/6i + ET yielded significantly longer PFS (20.0 vs 11.9 months, P = 0.0006). A trend towards improved OS was observed (28.6 vs 22.9 months, P = 0.1399). Conclusion This real-world analysis reinforces CDK4/6i + ET as the preferred first-line treatment for HR+/HER2− ABC with visceral metastases. While selection bias cannot be excluded, these findings support the shift away from routine first-line CT. Ongoing follow-up will clarify the OS impact.en
dc.subjectHR+/KER2-en
dc.subjectCDK4/6en
dc.subjectInhibitorsen
dc.subjectVisceralen
dc.subjectMetastasesen
dc.subjectChemotherapyen
dc.subjectEndocrine Therapyen
dc.subjectOncologyen
dc.titleReal-world outcomes in patients with hormone receptor positive, human epidermal growth factor receptor 2 receptor-negative advanced breast cancer and visceral metastases at baseline – advanced hormone receptor positive breast cancer registry in Australiaen
dc.typeJournal Articleen
dc.publisher.placeMelbourne, Australiaen
dc.identifier.journaltitleInternal Medicine Journalen
dc.accession.number10.1111/imj.70544en
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/full/10.1111/imj.70544en
dc.identifier.databaseWileyen
dc.identifier.notesEarly View Online Version of Record before inclusion in an issue.en
dc.format.pages9en
dc.identifier.importdoi10.1111/imj.70544en
dc.type.studyortrialCohort Studyen
dc.contributor.swhauthorCollins, Ian M.-
dc.relation.departmentOncology-
Appears in Collections:SWH Staff Publications

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