A Real-world Study on the Compliance of OFS-assisted Endocrine Therapy for Hormone Receptor-positive(HR+) Premenopausal Breast Cancer

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
AgeNot listed
SponsorZhejiang Cancer Hospital

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

300 Participants
are grouped into 1 trial group

Locations

This trial has no locations

Sponsors and collaborators

Zhejiang Cancer Hospital

Lead sponsor

Beijing Health Promotion Association

Collaborator