About this trial
The goal of this observational study is to observe the long-term prognosis of patients with early HR-positive premenopausal breast cancer. The study also aims to understand the compliance with and reasons for discontinuing adjuvant OFS endocrine therapy under different combination regimens.
The main questions it aims to answer are:
1. What are the rates of compliance with and reasons for discontinuation of adjuvant OFS endocrine therapy? 2. What is the impact of OFS treatment duration on patient prognosis?
Participants, who are already receiving OFS treatment as part of their regular medical care, will have their demographic data, treatment status, clinical outcomes, and adverse events collected over time.
Eligibility criteria
Qualifiers
Female breast cancer patients who were premenopausal at the time of surgery.
Newly diagnosed patients with invasive breast cancer, tumor node metastasis(TNM) stage I-III.
HR-positive (defined as ER ≥ 10% and/or progesterone receptor(PR) ≥ 10%).
Patients who have undergone radical mastectomy and are planning to receive OFS treatment.
Disqualifiers
Simultaneously participating in another blinded clinical study.
Presence of other active malignant tumors or multiple primary cancers.
Pregnant or lactating women.
Other conditions that the investigator deems unsuitable for inclusion in the study.
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Locations
Sponsors and collaborators
Zhejiang Cancer Hospital
Lead sponsor
Beijing Health Promotion Association
Collaborator