Skip to content

Early Changes in Metabolic Health in Breast Cancer Patients Initiating Endocrine Therapy

Early Breast Cancer, Endocrine Therapy Initiation, and Early Metabolic Health Changes: a Prospective Follow-up Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06623903
Acronym
EMETA
Enrollment
112
Registered
2024-10-02
Start date
2024-11-01
Completion date
2025-07-31
Last updated
2024-10-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Early Breast Cancer, Estrogen Receptor Positive Breast Cancer, Metabolic Health

Keywords

Early breast cancer, Metabolic health, Endocrine therapy

Brief summary

This clinical trial aims to investigate early metabolic health changes in early breast cancer patients that initiate antihormone therapy. Furthermore, how these changes are affected by estrogen level, treatment type, and patient characteristics. The hypothesis is, that initiation of antihormone therapy for early breast cancer patients is associated with an early deterioration in metabolic health after 3 months. This includes increased BMI (Body Mass Index), waist- and hip circumference, blood pressure, blood sugars, and lipids compared to when the patients initiate antihormone therapy. Concurrently, estradiol levels are expected to decrease. An estimated 112 patients initiating antihormone therapy at the Dept. of Oncology, Aarhus University Hospital (AUH) will be included in the study over 6 months from autumn 2024. Patients will have a metabolic screening on the day of initiating antihormone therapy and at 3-month antihormone treatment follow-up. The two metabolic screenings each consists of biometric measurements and a blood sample.

Detailed description

Metabolic health, closely tied to overweight and type 2 diabetes, significantly influences disease risks, notably breast cancer. With over 2.5 billion overweight adults globally, the prevalence of associated health concerns is escalating. Breast cancer, the leading cause of female cancer-related mortality, is intricately linked to metabolic factors, including overweight and diabetes, particularly affecting estrogen receptor-positive tumors. Conversely, endocrine therapy as breast cancer treatment can exacerbate metabolic issues, increasing weight gain and the risk of type 2 diabetes. Despite its efficacy in reducing recurrence risk, endocrine therapy is associated with adverse metabolic effects, including elevated cholesterol levels. Estrogen, pivotal in metabolic homeostasis, remains poorly understood in the context of endocrine therapy and metabolic disruptions. This prospective study aims to elucidate this relationship, focusing on the initiation of endocrine therapy, metabolic health, and estradiol levels among early-stage breast cancer patients. Early breast cancer patients initiating endocrine therapy at Aarhus University Hospital from autumn 2024 and six months ahead will be extended an invitation for study participation, with immediate measurements. Metabolic health will be analyzed through weight, hip and waist circumference measurements, blood sugar, cholesterol, and estrogen at baseline and 3-month follow-up. Thorough data collection, including demographics, treatment modalities, and cancer characteristics, ensures a comprehensive understanding of this complex interplay. With 112 projected participants, this study aims to shed light on the intricate connections between endocrine therapy, patient characteristics, and metabolic health changes. Through this comprehensive approach, the investigators aim to enhance patient care and understanding of managing metabolic health alongside breast cancer treatment.

Interventions

None listed

Sponsors

Danish Cancer Society
CollaboratorOTHER
Aarhus University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥18 years * Invasive ER+ breast cancer * No diabetes treatment * Planned for initiation of any adjuvant endocrine therapy.

Exclusion criteria

* Pregnancy or lactation, * Psychological, familial, sociological, or geographical conditions potentially hampering compliance with the study protocol and follow-up schedule; these conditions will be discussed with the patient before registration in the trial.

Design outcomes

Primary

MeasureTime frameDescription
Body Mass Index3 months (from initiation of endocrine therapy to 3 month treatment follow-up)A change in Body Mass Index (Height and weight combined, kg/m2)
Metabolic health changes3 months (from initiation of endocrine therapy to 3 month treatment follow-up)A change (deterioration or improvement) in metabolic health compared to baseline. Defined by a change in at least one of the below mentioned parameters.
Waist and hip circumference3 months (from initiation of endocrine therapy to 3 month treatment follow-up)A change in waist- and hip circumference compared to baseline
Blood pressure3 months (from initiation of endocrine therapy to 3 month treatment follow-up)A change in blood pressure compared to baseline
HbA1c3 months (from initiation of endocrine therapy to 3 month treatment follow-up)A change in circulating levels of glycated hemoglobin (HbA1c)
Cholestrerol3 months (from initiation of endocrine therapy to 3 month treatment follow-up)A change in blood cholesterol compared to baseline
Triglycerides3 months (from initiation of endocrine therapy to 3 month treatment follow-up)A change in triglycerides compared to baseline
LDL3 months (from initiation of endocrine therapy to 3 month treatment follow-up)A change in low-density lipoprotein (LDL) compared to baseline.
HDL3 months (from initiation of endocrine therapy to 3 month treatment follow-up)A change in and high-density lipoprotein (HDL) compared to baseline

Secondary

MeasureTime frameDescription
Estrogen level3 months (from initiation of endocrine therapy to 3 month treatment follow-up)Changes in circulating estrogen compared to baseline

Countries

Denmark

Contacts

Primary ContactLærke S Nissen, BS.c., Research Year Student
laenis@rm.dk(+45) 61 11 29 28
Backup ContactSigne Borgquist, Clinical Chair Professor, Ph.D
Signe.borgquist@auh.rm.dk(+45) 91 16 72 94

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026