Exploring an Alternative Pre-operative SLN Mapping Method Using a Magnetic Tracer and MRI for Melanoma Patients (SCARLETT)
Primary Purpose
Melanoma
Status
Recruiting
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Diagnostic Test: Sentinel node mapping using MRI
Sponsored by
About this trial
This is an interventional diagnostic trial for Melanoma focused on measuring Magnetic tracer, Sentinel lymph node, Melanoma, MRI
Eligibility Criteria
Inclusion Criteria:
- Patients ≥18 years of age at the time of consent;
- Histological confirmed melanoma (patient must have primary cutaneous melanoma with Breslow thickness ≥ 0.8-2.0mm with or without ulceration or <0.8mm with ulceration (pT1b - pT2b, AJCC 8th edition));
- Indication for wide local excision (margin 1 cm) and SLN procedure;
- Patients should be willing and able to provide informed consent.
Exclusion Criteria:
- Intolerance/hypersensitivity to 99mTc-nanocolloid, PB, iron or dextran compounds;
- Iron overload disease;
- Pregnant or breast-feeding women;
- Previous surrounded lymph node surgery;
- Patients with head and neck melanomas;
- Standard MRI exclusion criteria;
- Implantable (electrical) devices (e.g. pacemaker, cochlear implants, neurostimulator);
- Any other metal implants;
- Claustrophobia;
- MR-incompatible prosthetic heart valves;
- Patients who are unable or refuse to provide informed consent.
Sites / Locations
- Zuyderland Medical CenterRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Melanoma patients
Arm Description
All patients will undergo lymphatic mapping with SPIO, 99mTc and PB.
Outcomes
Primary Outcome Measures
The diagnostic accuracy of SPIO/MRI and LS+SPECT/CT and 99mTc to identify SLN
The diagnostic accuracy of SPIO/MRI and LS+SPECT/CT and 99mTc to identify SLN will be expressed as sensitivity and specificity, and positive and negative predictive values, including their 95% exact binomial confidence intervals. MRI image analyses will be performed by two independent professionals.
Secondary Outcome Measures
The diagnostic accuracy of SPIO/magnetometer and PB, 99mTc and Gamma probe
The diagnostic accuracy of SPIO/magnetometer and PB, 99mTc and Gamma probe will be expressed as sensitivity and specificity, and positive and negative predictive values, including their 95% exact binomial confidence intervals .
Comparison between 99mTc injection + LS + SPECT/CT time vs SPIO injection + MRI
Time/duration of 99mTc injection + LS + SPECT/CT and time/duration of SPIO injection + MRI will be compared
Number of post-injection (skin) reactions, complication and adverse events
Descriptive only
Full Information
NCT ID
NCT05145829
First Posted
November 3, 2021
Last Updated
January 24, 2023
Sponsor
Zuyderland Medisch Centrum
1. Study Identification
Unique Protocol Identification Number
NCT05145829
Brief Title
Exploring an Alternative Pre-operative SLN Mapping Method Using a Magnetic Tracer and MRI for Melanoma Patients
Acronym
SCARLETT
Official Title
Exploring an Alternative Pre-operative Sentinel Lymph Node Mapping Method Using a Magnetic Tracer and MRI for Melanoma Patients
Study Type
Interventional
2. Study Status
Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 1, 2022 (Actual)
Primary Completion Date
September 1, 2024 (Anticipated)
Study Completion Date
September 1, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Zuyderland Medisch Centrum
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Sentinel lymph node biopsy (SLNB) is crucial in the management of malignant melanoma treatment and is currently performed by pre-operatively inject a colloid nanomaterial labeled with Technetium (99mTc) as radioactive tracer. Intra-operatively, Patent Blue (PB) will be injected to improve the visualization of the lymphatic tract. However, current pre-operative SLN mapping technique is associated with disadvantages as radiation exposure for both patients and health care staff and logistic challenges, because of time constraints due to short half-live time of 99mTc.
Superparamagnetic iron oxide (SPIO) is a non-radioactive technique using a magnetic tracer (Magtrace® (Endomagnetics Ltd.)) to identify SLNs. Several studies showed that SPIO is non-inferior to dual tracing with 99mTc and PB in breast cancer patients. SPIO is expected to be non-inferior to dual tracing with 99mTc and PB in melanoma patients. However, further research is needed to demonstrate the use of SPIO in pre-operative MRI scanning.
The primary objective of this study is to evaluate the feasibility and diagnostic accuracy of pre-operative MRI scanning using SPIO compared to lymphoscintigraphy (LS) and single-photon emission computed tomography/computed tomography (SPECT/CT) using 99mTc for identifying SLN status in melanoma patients.
Detailed Description
Rationale: Sentinel lymph node biopsy (SLNB) is crucial in the management of malignant melanoma treatment and is currently performed by pre-operatively inject a colloid nanomaterial labeled with Technetium (99mTc) as radioactive tracer. Intra-operatively, Patent Blue (PB) will be injected to improve the visualization of the lymphatic tract. However, current pre-operative SLN mapping technique is associated with disadvantages as radiation exposure for both patients and health care staff and logistic challenges, because of time constraints due to short half-live time of 99mTc.
Superparamagnetic iron oxide (SPIO) is a non-radioactive technique using a magnetic tracer (Magtrace® (Endomagnetics Ltd.)) to identify SLNs. Several studies showed that SPIO is non-inferior to dual tracing with 99mTc and PB in breast cancer patients. SPIO is expected to be non-inferior to dual tracing with 99mTc and PB in melanoma patients. However, further research is needed to demonstrate the use of SPIO in pre-operative MRI scanning.
Objective: The primary objective of this study is to evaluate the feasibility and diagnostic accuracy of pre-operative MRI scanning using SPIO compared to lymphoscintigraphy (LS) and single-photon emission computed tomography/computed tomography (SPECT/CT) using 99mTc for identifying SLN status in melanoma patients. A secondary objective is to assess the feasibility and diagnostic accuracy of SPIO/magnetometer (Sentimag®, Endomagnetics Ltd.) in comparison with dual trace gold standard (99mTc and PB) in SLN procedures in melanoma patients.
Study design: A prospective single-arm feasibility study will be performed at the department of Surgical oncology at Zuyderland Medical Center Sittard, the Netherlands.
Study population: Adult patients (≥18 years) with primary melanoma stage I-II and an indication for wide local excision (1 cm) and SLN procedure will be included in the study.
Intervention (if applicable): All patients will undergo lymphatic mapping with a SPIO tracer (Magtrace®), 99mTc and PB.
Main study parameters/endpoints: The concordance in SLN detection rate (sensitivity and specificity) of SPIO/MRI and LS and SPECT/CT using 99mTc.
The concordance in SLN detection rate (sensitivity and specificity) of SPIO/magnetometer and the gold standard dual trace technique using 99mTc/Gamma probe and PB. Additionally, the number of post-injection (skin) reactions, complication and adverse events will be noted.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Melanoma
Keywords
Magnetic tracer, Sentinel lymph node, Melanoma, MRI
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Melanoma patients
Arm Type
Experimental
Arm Description
All patients will undergo lymphatic mapping with SPIO, 99mTc and PB.
Intervention Type
Diagnostic Test
Intervention Name(s)
Diagnostic Test: Sentinel node mapping using MRI
Intervention Description
Sentinel lymph node mapping in melanoma patients using a magnetic tracer and MRI
Primary Outcome Measure Information:
Title
The diagnostic accuracy of SPIO/MRI and LS+SPECT/CT and 99mTc to identify SLN
Description
The diagnostic accuracy of SPIO/MRI and LS+SPECT/CT and 99mTc to identify SLN will be expressed as sensitivity and specificity, and positive and negative predictive values, including their 95% exact binomial confidence intervals. MRI image analyses will be performed by two independent professionals.
Time Frame
Before surgery (MRI scanning and scintigraphy)
Secondary Outcome Measure Information:
Title
The diagnostic accuracy of SPIO/magnetometer and PB, 99mTc and Gamma probe
Description
The diagnostic accuracy of SPIO/magnetometer and PB, 99mTc and Gamma probe will be expressed as sensitivity and specificity, and positive and negative predictive values, including their 95% exact binomial confidence intervals .
Time Frame
During SLNB (surgery)
Title
Comparison between 99mTc injection + LS + SPECT/CT time vs SPIO injection + MRI
Description
Time/duration of 99mTc injection + LS + SPECT/CT and time/duration of SPIO injection + MRI will be compared
Time Frame
During SLNB (surgery)
Title
Number of post-injection (skin) reactions, complication and adverse events
Description
Descriptive only
Time Frame
At 10-14 days and at 3 months after the procedure
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients ≥18 years of age at the time of consent;
Histological confirmed melanoma (patient must have primary cutaneous melanoma with Breslow thickness ≥ 0.8-2.0mm with or without ulceration or <0.8mm with ulceration (pT1b - pT2b, AJCC 8th edition));
Indication for wide local excision (margin 1 cm) and SLN procedure;
Patients should be willing and able to provide informed consent.
Exclusion Criteria:
Intolerance/hypersensitivity to 99mTc-nanocolloid, PB, iron or dextran compounds;
Iron overload disease;
Pregnant or breast-feeding women;
Previous surrounded lymph node surgery;
Patients with head and neck melanomas;
Standard MRI exclusion criteria;
Implantable (electrical) devices (e.g. pacemaker, cochlear implants, neurostimulator);
Any other metal implants;
Claustrophobia;
MR-incompatible prosthetic heart valves;
Patients who are unable or refuse to provide informed consent.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
James van Bastelaar, MD, PhD
Phone
0884597777
Email
j.vanbastelaar@zuyderland.nl
First Name & Middle Initial & Last Name or Official Title & Degree
Loeki Aldenhoven, MSc
Phone
0884597777
Email
l.aldenhoven@zuyderland.nl
Facility Information:
Facility Name
Zuyderland Medical Center
City
Sittard
State/Province
Limburg
ZIP/Postal Code
6162BG
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
James van Bastelaar, MD, PhD
Phone
0031884597777
Email
j.vanbastelaar@zuyderland.nl
First Name & Middle Initial & Last Name & Degree
Loeki Aldenhoven, MSc
Phone
0031884597777
Email
l.aldenhoven@zuyderland.nl
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Exploring an Alternative Pre-operative SLN Mapping Method Using a Magnetic Tracer and MRI for Melanoma Patients
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