Clinical Application of ctDNA Dynamic Monitoring in Neoadjuvant Therapy for HER2-positive Breast Cancer Patients
- Sponsor
- The First Affiliated Hospital with Nanjing Medical University
- Study ID
- NCT06479460
- Status
- Recruiting
Conditions
- Breast Cancer
- Circulating Tumor DNA
- HER2-positive Breast Cancer
- Neoadjuvant
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- ctDNA-MRD — DIAGNOSTIC_TESTThis study is an observational non intervention study that only tests peripheral blood samples from different treatment nodes of the subjects, without interfering with the normal clinical diagnosis and treatment process of the patients.
Study Details
1. To explore the predictive value of ctDNA in HER2 positive breast cancer neoadjuvant therapy population; 2. To evaluate the prognostic value of ctDNA in HER2 positive breast cancer neoadjuvant therapy population.
Key Dates
- First listed
- Jun 28, 2024
- Start date
- Mar 8, 2024
- Status verified
- Jul 2024
- Primary completion
- May 31, 2025
- Completion
- Mar 31, 2026
Study Design
- Enrollment
- 50 participants (estimated)
Primary Outcome Measure
Postoperative pathological pCR rate [ Time Frame: 2024.3 -- 2026. 3 ]
Central Contacts
- Zhihone Zhang, Doctor of Medicine18013348615
- Jing Wu, Doctor of Medicine18013348615
Find similar trials
Related Studies
- Collection of Blood From Patients With CancerRecruiting · National Cancer Institute (NCI) · Bethesda, Maryland
- Harvesting Cells for Experimental Cancer TreatmentsEnrolling By Invitation · National Cancer Institute (NCI) · Bethesda, Maryland
- High Risk Breast Clinic: Protocol for Women at Increased Risk for Developing Breast CancerRecruiting · Carol Fabian, MD · Kansas City, Kansas
- Follow-Up Study of Subjects Previously Enrolled in Poxviral Vector Gene Transfer StudiesRecruiting · National Cancer Institute (NCI) · Bethesda, Maryland