MR Lymphography and Magnetic Sentinel Lymph Node Biopsy in Melanoma Patients (MelaDiff)
Primary Purpose
Melanoma (Skin)
Status
Not yet recruiting
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Magnetic sentinel lymph node biopsy by use of Magtrace®, in combination with SentiMag® and DiffMag
Sponsored by
About this trial
This is an interventional diagnostic trial for Melanoma (Skin) focused on measuring Magnetic sentinel lymph node biopsy (SLNB), Lymph node detection, Lymph node staging, MR lymphography, Super paramagnetic iron-oxide (SPIO) nanoparticles
Eligibility Criteria
Inclusion Criteria:
- Patients with melanoma of the upper or lower extremities scheduled for SLNB;
- Willing to & able to write informed consent from the subject prior to participation;
- Willing to & capable of following study procedures;
- Is older than 18 years;
- Speaks and understand the Dutch language
Exclusion Criteria:
- Intolerance / hypersensitivity to iron or dextran compounds
- Pregnant or lactating patients;
- Patients having a pacemaker.
- Patients non eligible for MRI investigation (pacemakers or other implantable devices in the chest wall and/or lower body, claustrophobic, etc.)
Sites / Locations
- Medisch Spectrum Twente
- Ziekenhuisgroep Twente (ZGT)
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
MelaDiff
Arm Description
Patients with melanoma of the extremities included in the protocol. Preoperative, patients will receive two MRI-scans and a magnetic tracer injection at the primary tumor site. During surgery, SLNs will be detected using two types of magnetometers (SentiMag® & DiffMag) in combination with Magtrace®, in addition to the standard procedure.
Outcomes
Primary Outcome Measures
True positive/False negative rate for a magnetic SLN detection measured by DiffMag system compared to radioactive detection.
Determining the feasibility of SLN detection/localization in melanoma patients using a magnetic tracer (Magtrace®) and hand-held magnetometer DiffMag.
True positive/False negative rate for a magnetic SLN detection measured by Sentimag system compared to radioactive detection.
Determining the feasibility of SLN detection/localization in melanoma patients using a magnetic tracer (Magtrace®) and hand-held magnetometer Sentimag.
Secondary Outcome Measures
True positive/False negative rate for metastatic SLN using ex vivo MRI
Determining the feasibility of LN mapping with preoperative SPIO-enhanced MR lymphography and examining the use of SPIO-enhanced MR lymphography for LN staging.
True positive/False negative rate for metastatic SLN using in vivo MRI
Determining the feasibility of LN mapping with preoperative SPIO-enhanced MR lymphography and examining the use of SPIO-enhanced MR lymphography for LN staging.
Full Information
NCT ID
NCT05569707
First Posted
September 17, 2022
Last Updated
October 3, 2022
Sponsor
University of Twente
1. Study Identification
Unique Protocol Identification Number
NCT05569707
Brief Title
MR Lymphography and Magnetic Sentinel Lymph Node Biopsy in Melanoma Patients
Acronym
MelaDiff
Official Title
MR Lymphography and Magnetic Sentinel Lymph Node Biopsy in Melanoma Patients Measured With DiffMag
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
January 2023 (Anticipated)
Primary Completion Date
January 2024 (Anticipated)
Study Completion Date
March 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Twente
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The sentinel lymph nodes (SLNs) are the first lymph nodes (LNs) to drain the tumor site and therefore the first LNs to bare metastases. Hence the importance to investigate these LNs for the best treatment strategy. Current-standard-of-care for melanoma patients with a melanoma stage of pT1b or higher, involve a surgical procedure, referred to as SLN biopsy (SLNB). The SLNB procedure involves a combined detection procedure using a radio-active tracer and blue dye followed by surgical dissection and evaluation of the LNs at the histopathology department. Due to the use of radioisotopes, this procedure suffers from several disadvantages such as limited availability, strict rules and regulations, degradation time in patient and radioactive load for user and patient.
To overcome the limitations of a radioactive tracer, a magnetic SLNB was developed which is facilitated by super paramagnetic iron-oxide (SPIO) nanoparticles. This potentially offers numerous benefits making surgery planning more flexible: no exposure to radiation, easy accessibility of the tracer, long shelf life and long half time in the patient. However, the currently available magnetometer for intraoperative detection of SPIO-enhanced LNs is hampered by a relatively low detection depth, biological noise, and effects of surgical equipment. Therefore, surgeons need to switch to plastic or carbon equipment and the system needs to be balanced prior to each measurement, which increases the surgery time.
A new and effective way to localize SPIOs is differential magnetometry (DiffMag). This patented detection principle, developed by MD&I group at University of Twente (UT), utilizes the nonlinear magnetic response of nanoparticles. An additional advantage of SPIOs is their visibility on MRI, which could provide mapping the SLNs preoperatively. Especially in patients with melanomas on the abdomen or back this would be very useful to see which lymph node stations are connected to the melanoma. In addition, studies have shown that SPIOs are absorbed into lymph nodes in different ways, depending on the presence of metastases. SPIO-enhanced MR lymphography could therefore provide an opportunity for a non-invasive preoperative assessment of nodal status.
In this pilot study the investigators want to evaluate the clinical use of the DiffMag handheld probe. Moreover, the investigators want to map the lymph nodes (metastases) preoperatively using MR lymphography.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Melanoma (Skin)
Keywords
Magnetic sentinel lymph node biopsy (SLNB), Lymph node detection, Lymph node staging, MR lymphography, Super paramagnetic iron-oxide (SPIO) nanoparticles
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
MelaDiff
Arm Type
Other
Arm Description
Patients with melanoma of the extremities included in the protocol. Preoperative, patients will receive two MRI-scans and a magnetic tracer injection at the primary tumor site. During surgery, SLNs will be detected using two types of magnetometers (SentiMag® & DiffMag) in combination with Magtrace®, in addition to the standard procedure.
Intervention Type
Device
Intervention Name(s)
Magnetic sentinel lymph node biopsy by use of Magtrace®, in combination with SentiMag® and DiffMag
Intervention Description
In addition to the standard procedure, SLNs will be detected using two types of magnetometers (SentiMag® & DiffMag) in combination with SPIO particles (Magtrace®).
Primary Outcome Measure Information:
Title
True positive/False negative rate for a magnetic SLN detection measured by DiffMag system compared to radioactive detection.
Description
Determining the feasibility of SLN detection/localization in melanoma patients using a magnetic tracer (Magtrace®) and hand-held magnetometer DiffMag.
Time Frame
through study completion, an average of 1 year
Title
True positive/False negative rate for a magnetic SLN detection measured by Sentimag system compared to radioactive detection.
Description
Determining the feasibility of SLN detection/localization in melanoma patients using a magnetic tracer (Magtrace®) and hand-held magnetometer Sentimag.
Time Frame
through study completion, an average of 1 year
Secondary Outcome Measure Information:
Title
True positive/False negative rate for metastatic SLN using ex vivo MRI
Description
Determining the feasibility of LN mapping with preoperative SPIO-enhanced MR lymphography and examining the use of SPIO-enhanced MR lymphography for LN staging.
Time Frame
through study completion, an average of 1 year
Title
True positive/False negative rate for metastatic SLN using in vivo MRI
Description
Determining the feasibility of LN mapping with preoperative SPIO-enhanced MR lymphography and examining the use of SPIO-enhanced MR lymphography for LN staging.
Time Frame
through study completion, an average of 1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with melanoma of the upper or lower extremities scheduled for SLNB;
Willing to & able to write informed consent from the subject prior to participation;
Willing to & capable of following study procedures;
Is older than 18 years;
Speaks and understand the Dutch language
Exclusion Criteria:
Intolerance / hypersensitivity to iron or dextran compounds
Pregnant or lactating patients;
Patients having a pacemaker.
Patients non eligible for MRI investigation (pacemakers or other implantable devices in the chest wall and/or lower body, claustrophobic, etc.)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Anke Christenhusz, MSc
Phone
+3153 489 1592
Email
a.christenhusz@utwente.nl
First Name & Middle Initial & Last Name or Official Title & Degree
Lejla Alic, PhD
Phone
+3153 489 1592
Email
l.alic@utwente.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lejla Alic, PhD
Organizational Affiliation
University of Twente
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Anneriet Dassen, PhD
Organizational Affiliation
Medisch Spectrum Twente Enschede
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medisch Spectrum Twente
City
Enschede
Country
Netherlands
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anneriet Dassen
Facility Name
Ziekenhuisgroep Twente (ZGT)
City
Hengelo
Country
Netherlands
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Daniëlle de Leeuw
12. IPD Sharing Statement
Plan to Share IPD
No
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MR Lymphography and Magnetic Sentinel Lymph Node Biopsy in Melanoma Patients
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