Actively Recruiting
The Association Between Age-related Peripheral Blood Components and Treatment Efficacy in Breast Cancer
Led by Fudan University · Updated on 2026-01-21
120
Participants Needed
1
Research Sites
68 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study is a single-center, prospective/retrospective, observational clinical research designed to compare the differences in peripheral blood components between young and elderly HR+HER2- breast cancer patients, and to identify peripheral blood components that may affect the prognosis of young HR+HER2- breast cancer patients. The study population consists of early-stage HR+HER2- breast cancer patients receiving neoadjuvant therapy. Eligible patients who require neoadjuvant treatment will be enrolled in the study. Retrospective data and samples will be collected based on existing patient medical records and tissue biobank samples. Prospective data collection will be based on routine clinical treatment during the study period and will continue until the patient completes neoadjuvant therapy and undergoes primary tumor surgery, or until the study is prematurely terminated. HR+HER2- breast cancer patients receiving neoadjuvant therapy will be divided into young and elderly groups. Peripheral blood samples will be collected at baseline (T0, prior to treatment) and after two cycles of neoadjuvant therapy (T1). Paired baseline tumor biopsy samples and/or surgical tumor samples will also be collected. Peripheral blood and tumor samples will undergo appropriate tests. The study respects the investigator's choice of treatment, without specifying which drugs should be used, the dosage, the administration mode (including monotherapy, combination therapy, or sequential therapy), or the duration of treatment.
CONDITIONS
Official Title
The Association Between Age-related Peripheral Blood Components and Treatment Efficacy in Breast Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Signed informed consent according to local regulations
- Age 18 years or older
- Female
- Histologically or cytologically confirmed breast cancer
- Breast cancer determined by immunohistochemistry to be estrogen receptor-positive or progesterone receptor-positive with at least 1% of cells expressing estrogen receptors and HER2-negative
You will not qualify if you...
- Presence of distant metastasis
- History of other malignancies except basal cell carcinoma or squamous cell carcinoma of the skin, cervical carcinoma in situ, or cancers disease-free for more than 5 years after treatment
- Participation in another clinical trial within 30 days before starting neoadjuvant treatment and receiving investigational drugs or treatments
- Immunodeficiency or HIV infection
- Severe dysfunction of heart, lung, liver, or kidneys
- Uncontrolled or active infections
- Pregnant or breastfeeding women
AI-Screening
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Trial Site Locations
Total: 1 location
1
Fudan University Shanghai Cancer Center Shanghai, China, 200032
Shanghai, Shanghai Municipality, China, 200032
Actively Recruiting
Research Team
Z
Zhimin Shao, MD, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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