Magseed Pro(R)/ Sentimag(R) Gen3

Endomagnetics Ltd.224 enrolled

Overview

The purpose of this study is to provide prospective evidence that the Magseed Pro® marker /Sentimag® Gen3 system is safe and effective for marking A. suspicious/biopsy-proven positive axillary lymph nodes; and B. soft tissue lesions including cancer and pre-cancerous change in the breast The devices used in this clinical trial are the Magseed Pro® marker and Sentimag® Gen3 system by Endomagnetics Limited. The Endomag Magseed Pro® Marker System is intended to be placed within the target soft tissue prior to planned surgical removal. The marker, when used in conjunction with the Sentimag® Gen 3 System, can be used as a guide for the surgeon to follow in the excision of tissue. The Sentimag® Gen3 Magnetic Localisation System when used with the Magseed family of markers is indicated to assist in localising soft tissue lesions. The study design is a multicentre international prospective, open label, study of Magseed Pro® marker and Sentimag® Gen3 system in patients with breast and/or lymph node pathology with: A. axillary lymph nodes requiring localisation prior to surgical excision (suspicious and/or biopsy proven lymph node or other pathology indicating removal) and/or B. breast lesions requiring localisation Patients will have the Magseed Pro® marker placed to mark A. surgical excision of suspicious/biopsy-proven axillary lymph node as part of a targeted lymph node biopsy procedure AND/OR B. breast lesions in patients undergoing surgical excision of the targeted breast lesion The Magseed Pro® marker will be localised using the Sentimag® Gen3 system and therafter surgically removed with the target tissue. This study will enrol 224 patients; 112 with Magseed Pro® marker placed to mark breast lesions and 112 with Magseed Pro® marker placed to mark nodes. The expected duration of enrolment is approximately 9 months across all sites with each individual subject's participation lasting approximately 1-38 weeks after enrolment.

Study Type

INTERVENTIONAL

Allocation

NON_RANDOMIZED

Purpose

OTHER

Masking

NONE

Enrollment

224

Conditions

Breast Cancer

Interventions

Magseed Pro(R) and Sentimag(R) Gen3 by EndomagneticsDEVICE

placement of Magseed Pro \& localisation with Sentimag Gen3 in axillary lymph nodes and/or breast lesions

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Participant is willing and able to give informed consent for participation in the study * Participant is aged 18 years or older at the time of consent. * Patients requiring breast lesion/axillary node marking and excision Exclusion Criteria:• Pregnant or nursing subjects and those who plan pregnancy during the clinical investigation follow-up period. A pregnancy test is required for all women of childbearing potential within 7 days before enrolment. * Presence of other anatomic or comorbid conditions, or other medical, social, or psychological conditions that, in the investigator's opinion, could limit the subject's ability to participate in the clinical trial or to comply with follow up requirements, or impact the scientific soundness of the clinical trial results * Known hypersensitivity to Nitinol * Subject has current active infection at the implantation site in the breast (per investigator discretion)

Locations (6)

Marienhospital Bottrop GmbH

Bottrop, Germany

RECRUITING

AGAPLESION Markus Frankfurter Diakonie Kliniken gGmbH

Frankfurt, Germany

RECRUITING

Technical University Munich

Munich, Germany

Outcomes

Primary Outcomes

The primary endpoints are the retrieval rates of the Magseed Pro® marker with the target lesion within the initial excised specimen for A.) axillary lymph nodes B.) breast lesions A.) axillary lymph nodes. B.) breast lesions

This is defined as the number of patients with successful Magseed Pro® marker placement as demonstrated on imaging, in whom the Magseed Pro® marker and the associated lymph node and/ or lesion is retrieved, divided by the total number of subjects.

Time frame: time of surgery

Secondary Outcomes

Tissue response (unexpected and expected)

EXPECTED Early (up to 2 days) - acute inflammation in the form of neutrophils with lymphocytes and some associated haemorrhage. Late (\>2 days) - active chronic inflammation in the form of neutrophils, lymphocytes, macrophages together with a fibroblastic response. Likely a foreign body reaction with increased numbers of histiocytes and some multinucleated giant cells. Possible granuloma formation (foreign body type). Scattered eosinophils. Later scarring (after 1-2 weeks) with fibrosis. Possible fat necrosis. UNEXPECTED Early and Late - • Very florid fibroblastic response with granulation tissue formation that mimics malignancy (nodular fasciitis-like), which may need immunohistochemical tests to differentiate between reactive chan

Time frame: time of surgery

Presence of unexpected histological tissue response for short- and long-term use of Magseed Pro marker

UNEXPECTED HISTOLOGICAL RESPONSE Early and Late - • Very florid fibroblastic response with granulation tissue formation that mimics malignancy (nodular fasciitis-like), which may need immunohistochemical tests to differentiate between reactive chan

Time frame: time of surgery

Rate of device-related AE's and SAE's

Time frame: through study completion, an average of 38 weeks

Central Contacts

Matt Womack, Dr

CONTACT

+447851247439 mwomack@endomag.com

Tanja Odeneg, Dr

CONTACT

+441223652604 todeneg@endomag.com

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.

Guy's Hospital

London, United Kingdom

RECRUITING

Royal Marsden Hospital

London, United Kingdom

RECRUITING

University Hospital South Manchester

Manchester, United Kingdom

RECRUITING

Retrieval rate for all lesions

Retrieval rate for all lesions (including target, non-target lesions and multiple lesions per patient) out of the total number of lesions with a Magseed Pro® marker placement. Non-target lesions include additional marked lesions which weren't defined as the target for the primary endpoint and any marked lesions from patients undergoing long term node retrieval.

Time frame: time of surgery

Retrieval rate for all nodes

Retrieval rate for all nodes (including multiple nodes per patient where applicable) out of the total number of nodes with a Magseed Pro® marker placement.

Time frame: time of surgery

Per lesion retrieval rate for target excised specimens

Time frame: time of surgery

Per lesion retrieval rate for all excised specimens

Time frame: time of surgery

Per lesion retrieval rate for all lesion

Time frame: time of surgery

Per lesion retrieval rate for all nodes

Time frame: time of surgery

Per patient retrieval rate for Magseed Pro® marker placed prior to neo-adjuvant therapy and retrieved post neo-adjuvant therapy

Time frame: time of surgery

Per lesion retrieval rate for Magseed Pro® marker placed prior to neo-adjuvant therapy and retrieved post neo-adjuvant therapy.

Time frame: time of surgery

Per patient retrieval rate for Magseed Pro® marker where retrieval surgery is within 30 days of placement.

Time frame: time of surgery

Per lesion retrieval rate for Magseed Pro® marker where retrieval surgery is within 30 days of placement.

Time frame: time of surgery

Per patient retrieval rate for Magseed Pro® marker where retrieval surgery is greater than 30 days after placement

Time frame: time of surgery

Per lesion retrieval rate for Magseed Pro® marker where retrieval surgery is greater than 30 days after placement.

Time frame: time of surgery

Per lesion retrieval rate for target excised specimens (i.e., lesions plus nodes) where Magtrace® Tracer is present in the target node or in the region of the target lesion.

Time frame: time of surgery

Per lesion retrieval rate for all excised specimens (i.e., lesions plus nodes) where Magtrace® Tracer is present in the target node or in the region of the target lesion.

Time frame: time of surgery

Per lesion retrieval rate for target lesions where Magtrace® Tracer is present in the region of the target lesion.

Time frame: time of surgery

Per lesion retrieval rate for all lesions where Magtrace® Tracer is present in the region of the lesion.

Time frame: time of surgery

Per node retrieval rate for target nodes where Magtrace® Tracer is present in the target node.

Time frame: time of surgery

Per node retrieval rate for all nodes where Magtrace® Tracer is present in the node.

er node retrieval rate for all nodes where Magtrace® Tracer is present in the node.

Time frame: time of surgery

Interventionist rated ease of Magseed Pro® marker placement by the interventionist

5 point Likert scale, very easy = 5, very difficult = 1

Time frame: seed placement

Rate of deployment failure

A Magseed Pro is not deployed from the needle, or is accidentally deployed prior to use in the patient • Success rate of seed placement: * Accurate: Within the breast lesion or clipped lymph node. For lesions less than 5 mm in size the marker may not necessarily be within the excised specimen but should be within 10mm1 of the lesion. * Inadequate: Not in the targeted lesion or clipped lymph node determined by placement imaging requiring additional marker placement

Time frame: seed placement

Surgeon rated ease of intra-operative localisation

5 point Likert scalevery easy = 5, very difficult = 1

Time frame: time of surgery

Magtrace® Tracer counts for excised lymph nodes during SLNB procedures

Time frame: time of surgery

Re-excision rate (i.e., second procedure required). With reason for second procedure.

Time frame: time of surgery

Success rate of maintained marker position at the time of removal as determined by specimen X-ray and or Sentimag Gen3 system.

* Accurate: Magseed Pro® marker within the target lesion or marked lymph node. * Inadequate: Magseed Pro® marker not within the target lesion or marked lymph node

Time frame: time of surgery