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Implementing geriatric assessment for dose optimization of CDK4/6 inhibitors in older breast cancer patients
Örebro Univ, Fac Med & Hlth, Dept Oncol, Örebro, Sweden..ORCID iD: 0000-0001-6059-0194
Hosp Prato, Azienda USL Toscana Ctr, Dept Oncol, Florence, Italy..
St Andrews Gen Hosp Patras, Dept Med Oncol, Patras, Greece..
Akershus Univ Hosp, Dept Oncol, Lorenskog, Norway..
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2024 (English)In: Future Oncology, ISSN 1479-6694, E-ISSN 1744-8301, Vol. 20, no 37, p. 2937-2948Article in journal (Refereed) Published
Abstract [en]

Current evidence from both randomized trials and real-world studies suggests that older patients with advanced hormone receptor-positive/HER2-negative (HR+/HER2) breast cancer derive clinical benefit from the addition of CDK4/6 inhibitors to endocrine therapy. However, a higher risk for adverse events due to CDK4/6 inhibitors among older patients is evident, leading to a trend of initiating CDK4/6 inhibitors at lower dose in clinical practice, though without evidence. The aim of the IMPORTANT-trial, a pragmatic, multinational, open-label, partly decentralized randomized trial is to investigate whether lower starting dose of CDK4/6 inhibitors combined with endocrine therapy is comparable to full dose in older (>= 70 years old) patients with advanced HR+/HER2- breast cancer who are assessed as vulnerable or frail based on comprehensive geriatric assessment.

Place, publisher, year, edition, pages
Taylor & Francis, 2024. Vol. 20, no 37, p. 2937-2948
Keywords [en]
advanced breast cancer, CDK4/6 inhibitors, comprehensive geriatric assessment, lower dose, randomized
National Category
Cancer and Oncology Geriatrics
Identifiers
URN: urn:nbn:se:uu:diva-548565DOI: 10.1080/14796694.2024.2413841ISI: 001337572800001PubMedID: 39431459Scopus ID: 2-s2.0-85207255072OAI: oai:DiVA.org:uu-548565DiVA, id: diva2:1931640
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EU, Horizon Europe, 101104589Available from: 2025-01-27 Created: 2025-01-27 Last updated: 2025-01-27Bibliographically approved

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Lindman, HenrikSchiza, Aglaia

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