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Study identifier: NCT07273357 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Aspects of Adjuvant CDK4/6 Inhibitors in Older Breast Cancer Patients - Focusing on Geriatric Screening

Condition: Geriatric Assessment · Adjuvant Drug Therapy · Breast Cancer Early Stage Breast Cancer (Stage 1-3)  ·  Sponsor: Region Jönköping County

PhaseN/A
Planned participants200
Who can joinAll sexes, 70 Years to no upper limit
Healthy volunteersNo

About this study

Older breast cancer patients should not be categorically excluded from adjuvant therapies, including the recommended CDK4/6 inhibitors (CDK4/6i) administered in combination with endocrine therapy. Nevertheless, this population frequently presents with comorbidities that may increase susceptibility to treatment-related toxicities, including impacts on quality of life, which must be carefully considered when selecting therapeutic regimens. Given the limited representation of older patients in the clinical trials behind the recommendations for adjuvant CDK4/6i therapy, coupled with the uncertain magnitude of clinical benefit and the reported rates of toxicity and treatment discontinuation, it is essential to critically evaluate both efficacy and safety in this specific patient subgroup. National and international guidelines recommend the integration of geriatric assessments into routine clinical practice to facilitate individualized treatment decisions; however, such assessments are not yet widely implemented in many oncology departments and are not routinely in use to guide adjuvant CDK4/6i therapy. This study aims to investigate the implementation of geriatric assessments in older breast cancer patients (≥70 years) and to examine multiple dimensions of CDK4/6i treatment in this cohort, including short- and medium-term effects on quality of life, dose intensity, and clinical outcomes. By doing so, the investigators seek to more accurately delineate the benefits and risks of ad…

This description comes directly from the study's public registry record.

Talk to the study team

Christine Lundgren, MD  ·  +46102422907  ·  christine.lundgren@rjl.se

Always discuss trial participation with your own doctor first.

Locations (5)

Department of OncologyGävle, SwedenRecruiting
Department of OncologyJönköping, SwedenRecruiting
Department of OncologyKalmar, SwedenRecruiting
Department of OncologyLinköping, SwedenRecruiting
Department of OncologyÖrebro, SwedenNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT07273357