Magseed and Magtrace Localization for Breast Cancer

Breast Carcinoma Clinical Trial

Official title:

Targeted Axillary Dissection, Sentinel Biopsy, and Tumor Lesion Localization in Breast Cancer Patients Using the New Magnetic "Sentimag" Detection System

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05161507
• Other study ID #: CHIR-07-Sentimag
• Secondary ID: 05/RVO-FNOs/2020
• Status: Completed
• Start date: May 4, 2020
• Est. completion date: December 31, 2023

Study information

• Verified date: January 2024
• Source: University Hospital Ostrava
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The aim of this study is to compare the efficacy of the Sentimag localization system and its tracer Magtrace, superparamagnetic iron oxide nanoparticles, as a tracer in sentinel node biopsy in breast cancer with Tc99 in a single-center prospective study. The other part of the study will be the implantation of the smallest non-radioactive seed, Magseed, in the non-palpable breast cancer lesions. Another part of the study will be the implantation of Magseed in the positive axillary lymph nodes in patients diagnosed with clinically positive lymph nodes that will receive neoadjuvant systemic therapy.

Description:

The aim of this study is to compare the efficacy of the Sentimag localization system and its tracer Magtrace, superparamagnetic iron oxide nanoparticles, as a tracer in sentinel node biopsy in breast cancer with Tc99 in a single-center prospective study. It also aims to follow skin discoloration after Magtrace injection and describe when and how it resolves. The Magtrace will be injected preoperatively. Sentinel node biopsy will be performed and detection rates will be recorded for both methods. The other part of the study will be the implantation of the smallest non-radioactive seed, Magseed, in the non-palpable breast cancer lesions. Intraoperative localization of the seed is achieved with the use of the Sentimag probe. Another part of the study will be the implantation of Magseed in the positive axillary lymph nodes in patients diagnosed with clinically positive lymph nodes that will receive neoadjuvant systemic therapy. To accurately assess the response in the breast and the axilla, it is important that both the positive lymph node/s are marked before neoadjuvant systemic therapy to be able to locate them later on. Systemic therapy can negatively impact lymphatic drainage and hence reduce the accuracy of the sentinel lymph node biopsy (SLNB). However, when SLNB is paired with the removal of the previously positive target lymph node, a technique called Targeted Axillary Dissection, the operation becomes a lot more accurate, with lower morbidity of the patients. A part of the study is also the verification of the time stability of breast tumor labeling with Magseed in the period from the onset of neoadjuvance to the subsequent operation following the oncological pretreatment of the patient. All patients will undergo sentinel lymph node detection also by the classic detection system with Tc99. Patients receive the Magseed marker via ultrasound-guided injection into a lymph node or to non-palpable breast cancer lesion. After completion of the study, patients are followed up within 6-30 days post-surgery at our surgical clinic.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 70
• Est. completion date: December 31, 2023
• Est. primary completion date: December 31, 2021
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Histologically confirmed cT0-4 breast cancer
• Without/ With axillary lymph node metastasis with pathologic confirmation by needle biopsy
• With/ without received neoadjuvant chemotherapy prior to surgical resection

Exclusion Criteria:

• Distant metastases
• The subject is known to be pregnant
• Pacemaker of another implantable device in the chest wall
• Allergy to dextran or other iron-containing particles

Related Conditions & MeSH terms

• Breast Carcinoma
• Breast Carcinoma Metastatic in Lymph Node
• Breast Neoplasms
• Carcinoma

Intervention

Procedure:
• Magseed
Patients with the non-palpable histologically confirmed breast cancer lesion - the tumor lesion will be labeled with Magseed and patient will undergo breast-conserving surgery and sentinel lymph node detection with Tc99.
• Magtrace
Patients with the palpable histologically confirmed breast cancer lesion - The Magtrace will be injected preoperatively into the tumor and detected by Sentimag. Patient will undergo sentinel lymph node detection with Tc99 and Sentimag localization system with breast surgery.
• Axillary lymph node metastasis - needle biopsy
Patients with the histologically confirmed breast cancer lesion with Axillary lymph node metastasis with pathologic confirmation by needle biopsy - the positive axillary lymph node lesion will be labeled with Magseed before the neoadjuvant systemic therapy, and later during target axillary dissection will be performed the biopsy of labeled lymph node during breast surgery.

Locations

Country	Name	City	State
Czechia	University Hospital Ostrava	Ostrava	Moravian-Silesian Region

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital Ostrava

Country where clinical trial is conducted

Czechia, 

References & Publications (3)

Greenwood HI, Wong JM, Mukhtar RA, Alvarado MD, Price ER. Feasibility of Magnetic Seeds for Preoperative Localization of Axillary Lymph Nodes in Breast Cancer Treatment. AJR Am J Roentgenol. 2019 Oct;213(4):953-957. doi: 10.2214/AJR.19.21378. Epub 2019 Jun 5. — View Citation

Rubio IT, Diaz-Botero S, Esgueva A, Rodriguez R, Cortadellas T, Cordoba O, Espinosa-Bravo M. The superparamagnetic iron oxide is equivalent to the Tc99 radiotracer method for identifying the sentinel lymph node in breast cancer. Eur J Surg Oncol. 2015 Jan;41(1):46-51. doi: 10.1016/j.ejso.2014.11.006. Epub 2014 Nov 15. — View Citation

Zacharioudakis K, Down S, Bholah Z, Lee S, Khan T, Maxwell AJ, Howe M, Harvey J. Is the future magnetic? Magseed localisation for non palpable breast cancer. A multi-centre non randomised control study. Eur J Surg Oncol. 2019 Nov;45(11):2016-2021. doi: 10.1016/j.ejso.2019.06.035. Epub 2019 Jun 26. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Accuracy of Magseed placement	Accuracy of Magseed placement will be measured regarding its position towards the lymph node in mm. Will be defined as accurate, marginal or inadequate. Descriptive statistics will be used to summarize accuracy of placement. Other statistical methods, when appropriate, may be used for analysis.	During the surgical procedure
Primary	Surgeon-rated ease of detected lymph node localization and removal	Descriptive statistics will be used to summarize surgeon rated ease of localization.	During the surgical procedure
Primary	Number of nodes retrieved within the surgical specimen containing the Magseed	Descriptive statistics will be used to summarize number of nodes retrieved within the surgical specimen containing the Magseed.	During the surgical procedure
Primary	Surgeon-rated ease of detected labeled lesion localization and removal	Descriptive statistics will be used to summarize number of nodes retrieved within the surgical specimen containing the Magseed.	During the surgical procedure
Primary	Transcutaneous detection rate	Descriptive statistics will be used to summarize transcutaneous detection rate.	During the surgical procedure
Primary	Incidence of adverse events	Toxicity data will be summarized by frequency tables. For the toxicity endpoint, per-treated analysis will be used to include any patient who received the treatment regardless of the eligibility nor the duration or dose of the treatment received.	Up to 6 weeks post-procedure