Implementing geriatric assessment for dose optimization of CDK4/6 inhibitors in older breast cancer patients

Antonis Valachis, Laura Biganzoli, Athina Christopoulou, Kamilla Fjemeros, Elena Fountzila, Jürgen Geisler, Raquel Gomez-Bravo, Peeter Karihtala , Paris Kosmidis, Angelos Koutras, Helena Linardou, Henrik Lindman, Iván Martínez-Ballestero, Anna Belén Rodríguez, Icro Meattini, Montserrat Munoz-Mateu, Mukhrizah Othman, Amanda Psyrri, Emanuela Risi, Aglaia SchizaNikolaos Spathas, Meri Utriainen , Luca Visani, Soledad Ballesteros, Ioannis Basdekis, Susanne Dieroff Hay, Theo Fotis, Samuel Fricker, Gimon de Graaf, Marit Jenset, Tim Kanters, Kostas Lampropoulos, Christiana Markou, Kalliopi Mastoraki, Christina Nanou, José Manuel Reales Aviles, Marianne Santaholma , Thanos Kosmidis

Research output: Contribution to journalArticlepeer-review

Abstract

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.
Original languageEnglish
Pages (from-to)1-12
JournalFuture Oncology
DOIs
Publication statusPublished - 21 Oct 2024

Keywords

  • advanced breast cancer
  • CDK4/6 inhibitors
  • comprehensive geriatric assessment
  • lower dose
  • randomized

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