About this trial
The use of neoadjuvant chemotherapy in breast cancer is expanding in the recent decade. Patients with good response to neoadjuvant chemotherapy could benefit from de-escalation of breast and axilla operation. However, breast tumor and involved axillary lymph node should be marked before the commencement of chemotherapy. This could facilitate subsequent operative planning and intraoperative assessment of disease response. This study aims to evaluate the feasibility of magnetic marker localization for non-palpable breast cancer and targeted axillary dissection in patients with node-positive breast cancer following neoadjuvant therapy
Eligibility criteria
Qualifiers
All patients with cT1-3N1 invasive ductal carcinoma planned for neoadjuvant chemotherapy and/or target therapy
mentally competent to give informed consent
Agreed to proceed with curative operation after chemotherapy and tentatively keen for breast conservative surgery and targeted axillary dissection after neoadjuvant chemotherapy
Radiologically 1-3 ipsilateral axillary lymph node metastases confirmed by cytology or biopsy
Disqualifiers
Presence of distant metastasis, inflammatory breast cancers, multi-centric breast cancers
History of previous ipsilateral axillary surgery or irradiation
Hypersensitivity to dextran compounds or iron
Iron overload disease
Trial design
Treatments tested in this trial
- Magnetic seed localization
Treatment groups
Sponsors and collaborators
The University of Hong Kong
Lead sponsor
Endomagnetics Ltd.
Collaborator