Short-term Impacts of Endocrine Therapy on Cardiovascular and Brain Health Outcomes in Breast Cancer

Recruiting now

Conditions studied: Breast Cancer Females

In brief

Aromatase inhibitors are the most used endocrine therapy for hormone-positive breast cancer. While there is a clear linear relationship between the duration of aromatase inhibitor use and the cumulative incidence of cardiovascular events and mortality, the underlying mechanisms contributing to this risk remain unknown. This study will characterize the short-term effects of aromatase inhibitor therapy on established and novel health indices for cardiovascular diseases in breast cancer patients. Using a longitudinal case-control design this study will assess the effects of short-term (first 6 months) aromatase inhibitor use in breast cancer patients compared to age- and BMI-matched controls, aiming to determine the cardiovascular, metabolic, and behavioural health impacts of endocrine treatment during this early period. Specifically, our objectives are as follows: 1. To examine the effects of aromatase inhibitor therapy on early risk indicators for cardiovascular disease in the peripheral vasculature and heart, including blood biomarkers (lipids), blood pressure, aortic and peripheral stiffness, carotid artery stiffness and intima media thickness, endothelial function, and left ventricular ejection fraction, longitudinal strain, volumes, and mass, including the responsiveness of the cardiovascular system to an oral glucose tolerance test, in breast cancer survivors compared to controls. 2. To examine the effects of aromatase inhibitor therapy on factors related to cerebrovascular health, autonomic regulation, and cognitive function, including BDNF, heart rate variability, cerebrovascular function in response to a supine-sit-stand maneuver and squatting challenge, and a core battery of cognitive function tests, in breast cancer survivors compared to controls. 3. To examine the effects of aromatase inhibitor therapy on body composition and bone mineral density, along with assessments of glycemic regulation in response to an oral glucose tolerance test and in 24h periods of free-living (continuous glucose monitoring), in breast cancer survivors compared to controls. 4. To examine the effects of aromatase inhibitor therapy on lifestyle factors (behavioural), including diet, physical activity (including cardiorespiratory fitness), sleep, stress, and quality of life, in breast cancer survivors compared to controls. The investigators hypothesize that cardiovascular and metabolic health outcomes will be similar between breast cancer survivors and controls at baseline but will deteriorate relative to controls within the first 6 months of aromatase inhibitor therapy.

Key facts

Study ID: NCT06781762
Run by: University of Toronto
People needed: 40
Starts: 2025-06-06
Expected to finish: 2026-12-30
Last updated by the study team: 2025-10-01

Who can join

Age: any. Sex: female. Healthy volunteers: accepted.

You may qualify if…

Case group:
Biologically female
Post-menopausal with natural (no bilateral oophorectomy) amenorrhea for at least 1 year
If using hormone replacement therapy, limit of a maximum of 3 years of treatment but not within the last 6 months.
Diagnosis of stage I, II, or III breast cancer
Hormone receptor positive breast cancer
HER negative (ER+/PR+/HER-) breast cancer
Confirmed to start aromatase inhibitor therapy for the first time in next 2-3 months
Received surgery/radiation therapies
Control group:
Biologically female
Post-menopausal with natural (no bilateral oophorectomy) amenorrhea for at least 1 year
If using hormone replacement therapy, limit of a maximum of 3 years of treatment but not within the last 6 months.

You may not qualify if…

Previous treatment using tamoxifen endocrine therapy in a pre-or peri-menopausal setting
Major signs or symptoms of cardiovascular diseases, diabetes, or renal disease (taken from the American College of Sports Medicine's Guidelines for Exercise Testing and Prescription 11th edition Table 2.1: pain or discomfort in the chest, neck, jaw, arms with rest or exercise, shortness of breath at rest or with mild exertion, dizziness or syncope, loss of balance or passing out, ankle edema, palpitations or tachycardia, intermittent claudication, known heart murmur, unusual fatigue with usual activities.)
American Heart Association's absolute or relative contraindications for symptom-limited maximal exercise testing (myocardial infarction, aortic or coronary artery stenosis, heart failure, pulmonary embolism or deep vein thrombosis, inflammation of the heart (myocarditis, pericarditis, and/or endocarditis), uncontrolled cardiac arrythmia, advanced or complete electrical heart block, stroke or transient ischemia attack, blood pressure >200mmHg/100mmHg, a cancer diagnosis other than skin cancer)
Unable to provide informed consent or communicate in English
Mobility limitations to exercise testing (i.e., wheelchair, walker use, limp impeding walking)
Extreme claustrophobia

Where it is running

University of Toronto — Toronto, Ontario, Canada (enrolling)

Full record on ClinicalTrials.gov

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