Skip to content

Effect of (neo)Adjuvant Therapy on Lipids in Young Breast Cancer Patients

A Multicentre Prospective Cohort Study: Effect of (neo)Adjuvant Therapy on Lipids in Young Breast Cancer Patients

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06405269
Enrollment
600
Registered
2024-05-08
Start date
2024-05-06
Completion date
2029-05-01
Last updated
2025-02-14

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

Conditions

Breast Neoplasms, Lipid Profile

Brief summary

Previous studies have shown differences in the effects of different endocrine drugs on blood lipids in breast cancer, and dyslipidaemia is a major risk factor for cardiovascular disease, and it has been previously reported that the leading cause of death in postmenopausal patients with breast cancer is cardiovascular disease, but the effects of endocrine drug therapy on blood lipids in young breast cancer patients (age ≤40) are not clear. Previously, our group conducted a preliminary retrospective analysis of young patients on endocrine therapy and found that dyslipidaemia was also a common adverse effect of treatment in young breast cancer patients; therefore, dyslipidaemia induced by antineoplastic therapy not only occurs in postmenopausal patients, but is also prevalent in premenopausal and even younger patients. Therefore, this study intends to evaluate the effects of different treatment regimens on lipids in early-stage young breast cancer patients and to explore the optimal timing of lipid-lowering drug interventions to provide a basis for clinical practice.

Interventions

None listed

Sponsors

Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* ECOG score 0-1 * Resectable breast cancer * No distant metastases on postoperative imaging assessment * Patients proposed for (neo)adjuvant therapy * No previous oral lipid-lowering drugs, serum LDL-C level within normal range, i.e. LDL-C value: <3.4 mmol/L * No fatty liver by liver ultrasound/CT examination * No major organ dysfunction

Exclusion criteria

* Patients with pre-existing hyperlipidaemia, coronary heart disease, fatty liver disease, or who have received or are receiving lipid-lowering medication * Enrolled in another study or less than or equal to 4 weeks since discontinuation of other medications * Presence of severe dysfunction of vital organs * Patients with other malignancies (except cured non-melanoma skin cancer, cervical carcinoma in situ and other tumours that have been cured for at least 5 years) * Acute infectious diseases or chronic infectious diseases in active stage * History of uncontrolled epilepsy, central nervous system disease or mental disorder

Design outcomes

Primary

MeasureTime frameDescription
Proportion of patients who developed LDL-C abnormalities in 3 groups2 yearsObserve and compare differences between groups

Secondary

MeasureTime frameDescription
Proportion of patients who developed TC,LDL-C,and TG abnormalities in 3 groups2 yearsObserve and compare differences between groups
Proportion of patients developing fatty liver in 3 groups2 yearsObserve and compare differences between groups

Countries

China

Outcome results

None listed

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