Breast Cancer Clinical Trial
— MAGELLANOfficial title:
A Prospective Open Label Study of the Use of Magseed® Markers and Sentimag® to Localize Axillary Lymph Nodes With Biopsy-proven Metastases in Breast Cancer Patients
NCT number | NCT03796559 |
Other study ID # | US-003 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | June 13, 2019 |
Est. completion date | April 2025 |
The purpose of this study is to provide prospective evidence that the use of Magseed/Sentimag in marking axillary lymph nodes and guiding surgical localization in patients with breast cancer following neo-adjuvant chemotherapy (NAC) is effective.
Status | Recruiting |
Enrollment | 65 |
Est. completion date | April 2025 |
Est. primary completion date | December 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Age 18 years or older at time of consent - Histologically confirmed cT0-4, N1 breast cancer - Axillary lymph node metastasis with pathologic confirmation by needle biopsy - Clip placed in the sampled axillary lymph node before initiation of chemotherapy - Planned for neo-adjuvant chemotherapy prior to surgical resection - Eligible for targeted axillary dissection (defined as selective localization and removal of the clipped node and SLND) at the completion of neo-adjuvant chemotherapy - ECOG performance status 0-2 Exclusion Criteria: - Distant metastases - Inflammatory breast cancer - Prior ipsilateral axillary surgical procedure including SLND or axillary node excision - Prior history of breast cancer in the ipsilateral breast - History of lymphoma - Subject is pregnant - Previous radiation to the breast or axilla - Pacemaker or other implantable cardiac device in the ipsilateral chest wall |
Country | Name | City | State |
---|---|---|---|
United States | Baylor Medicine | Houston | Texas |
United States | MD Anderson Cancer Center | Houston | Texas |
Lead Sponsor | Collaborator |
---|---|
Endomagnetics Inc | M.D. Anderson Cancer Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Retrieval rate of clipped node and Magseed in the excised specimen | The retrieval rate of the clipped node and Magseed in the excised specimen. This is defined as the number of subjects in whom the clipped node and Magseed are retrieved in a single excised specimen divided by the total number of subjects. | Time of surgery | |
Secondary | Rates of device and serious device-related events | Rates of device-related adverse events and serious device-related adverse events | Up to 42 days post-surgery | |
Secondary | Radiologic rated ease of Magseed placement | 5 point Likert scale, very easy = 5, very difficult = 1 | Time of Magseed marker placement | |
Secondary | Radiologic placement accuracy | Success rate of seed placement (placement accuracy) | Between completion of NAC time of surgery | |
Secondary | Radiologic seed position | Success rate of maintained seed position at the completion of NAC | After completion of NAC | |
Secondary | Surgical nodes localized | Number of nodes retrieved within the surgical specimen containing the Magseed | Time of surgery | |
Secondary | Ease of surgical localization | 5 point Likert scalevery easy = 5, very difficult = 1 | Time of surgery |
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