Axillary Lymph Node Metastasis

2

Review clinical trials related to Axillary Lymph Node Metastasis. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

A Prospective Multicenter Study of the TuFEst-LN Model for Axillary Lymph Node Status Assessment in Breast Cancer

Through the research of this project, we expect to validate the clinical utility of the TuFEst-LN model in assessing axillary lymph node status in breast cancer patients. Specifically, we aim to prospectively validate its ability to identify pathologically node-negative patients among clinically and radiologically assessed cN0 patients undergoing upfront surgery ,and explore the predictive value of the TuFEst-LN model combined with preoperative MRI for ypN status assessment in initially node-positive patients following neoadjuvant therapy.

Participants needed: 400
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Second Affiliated Hospital, Zhejiang University, School of MedicineUpdated: Aug 10, 2026Locations: 1Duration: 1 Year
Eligibility criteria

Histologically confirmed invasive breast cancer. [+14]

Pregnancy or breastfeeding. [+8]

Status: Not yet recruiting

Ultrasound Monitoring of Clipped Lymph Nodes to Predict Axillary Response After Chemotherapy in Breast Cancer

This study aims to evaluate whether longitudinal multimodal ultrasound can accurately predict axillary pathological response in breast cancer patients who receive neoadjuvant chemotherapy. In this study, patients with biopsy-proven metastatic axillary lymph nodes will have a metallic clip placed in the positive node before chemotherapy. During and after treatment, the clipped lymph node will be monitored by ultrasound, including gray-scale imaging, shear wave elastography, and contrast-enhanced ultrasound. The changes in the morphological and functional features of the clipped node will be analyzed to establish a predictive model for axillary pathological complete response. The results are expected to help identify patients who may safely avoid unnecessary axillary lymph node dissection and improve individualized surgical decision-making.

Participants needed: 150
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Sun Yat-Sen Memorial Hospital of Sun Yat-Sen UniversityUpdated: May 19, 2026Locations: 1
Eligibility criteria

Female patients aged 18 years or older.

Bilateral breast cancer.