NIR-Guided Sentinel Lymph Node Mapping in Melanoma
Primary Purpose
Melanoma
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
ICG Intervention
Sponsored by
About this trial
This is an interventional diagnostic trial for Melanoma focused on measuring lymph node
Eligibility Criteria
Inclusion Criteria:
- Histologically confirmed melanoma and an appropriate surgical candidate for a sentinel lymph node biopsy
- Stage of disease conducive to sentinel lymph node biopsy as determined by oncologic surgeon
- Receiving a planned lymphoscintigraphy procedure
Exclusion Criteria:
- History of allergic reactions attributed to compounds of similar chemical or biologic composition to indocyanine green, including those patients with a history of iodide or seafood allergy
- Pregnant or breast-feeding
Sites / Locations
- Beth Israel Deaconess Medical Center
- Brigham and Women's Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
ICG Intervention
Arm Description
Intraoperative NIR fluorescence imaging was performed after injection of 1.0 ml of 100 µM, 250 µM or 500 µM of ICG:HSA in four quadrants around the primary lesion. (The intervention to be administered is the ICG.)
Outcomes
Primary Outcome Measures
Feasibility
To determine the feasibility of real-time intraoperative NIR lymphatic mapping with concurrent identification of the sentinel lymph node in human melanoma using indocyanine green.
Secondary Outcome Measures
Comparison of SLN identification rate between near-infrared mapping and lymphoscintigraphy.
Full Information
NCT ID
NCT01121718
First Posted
May 6, 2010
Last Updated
February 2, 2017
Sponsor
Dana-Farber Cancer Institute
Collaborators
Beth Israel Deaconess Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT01121718
Brief Title
NIR-Guided Sentinel Lymph Node Mapping in Melanoma
Official Title
Real-Time NIR-Guided Sentinel Lymph Node Mapping in Melanoma
Study Type
Interventional
2. Study Status
Record Verification Date
February 2017
Overall Recruitment Status
Completed
Study Start Date
September 2010 (undefined)
Primary Completion Date
April 2012 (Actual)
Study Completion Date
April 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Dana-Farber Cancer Institute
Collaborators
Beth Israel Deaconess Medical Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study will try to define an appropriate dose of the investigational drug indocyanine green (ICG) in combination with near infrared (NIR) imaging to use for future studies.
ICG is a dye which has been in use since the 50s, and is approved for testing liver function and measuring blood flow from the heart. It has been used in studies to map lymphatic pathways in lung and breast cancer and information from those studies suggest it may help identify lymph nodes associated with melanoma. ICG can be detected within the body using near-infrared light cameras.
In this study the investigators are looking at how easily ICG can get to the first lymph node (sentinel lymph node [SLN]) associated with melanoma, whether the investigators can see the path of the ICG and the SLN using a near infrared camera, and what dose of ICG works the best. While the current method for SNL mapping, known as lymphoscintigraphy, is effective it does provide a small amount of radiation. This study will compare the investigators results to the standard procedure.
Detailed Description
At the time of surgery, you will undergo a lymphoscintigraphic procedure which is standard of care for patients with melanoma. You will also receive a dose of ICG mixed with human serum albumin. This will be administered in four small injections immediately around your tumor or the tumor scar if it has already been removed. Pictures of the ICG solution will be taken with the NIR camera and the progression of the dye along the lymphatic channel from your tumor to the SLN will be monitored.
As each lymph node is removed, pictures will be taken to see if the ICG dye has entered and colored that node. We will compare this technique with the results from the lymphoscintigraphy to measure accuracy.
Patients will be followed for at least one hour post injection for adverse events. The patient will then be taken off of the study. The results from each intervention will subsequently analyzed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Melanoma
Keywords
lymph node
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Model Description
This is an experimental study. All study subjects will receive the same intervention.
Masking
None (Open Label)
Masking Description
This study does not involve any masking.
Allocation
N/A
Enrollment
26 (Actual)
8. Arms, Groups, and Interventions
Arm Title
ICG Intervention
Arm Type
Experimental
Arm Description
Intraoperative NIR fluorescence imaging was performed after injection of 1.0 ml of 100 µM, 250 µM or 500 µM of ICG:HSA in four quadrants around the primary lesion. (The intervention to be administered is the ICG.)
Intervention Type
Drug
Intervention Name(s)
ICG Intervention
Other Intervention Name(s)
NIR fluorescence imaging, Sentinel Lymph Node
Intervention Description
NIR-guided sentinel lymph node mapping with indocyanine green (ICG)
Primary Outcome Measure Information:
Title
Feasibility
Description
To determine the feasibility of real-time intraoperative NIR lymphatic mapping with concurrent identification of the sentinel lymph node in human melanoma using indocyanine green.
Time Frame
We will analyze data immediately following each case, and analyze all collected data at 6 month intervals
Secondary Outcome Measure Information:
Title
Comparison of SLN identification rate between near-infrared mapping and lymphoscintigraphy.
Time Frame
We will analyze data immediately following each case, and analyze all collected data at 6 month intervals
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Histologically confirmed melanoma and an appropriate surgical candidate for a sentinel lymph node biopsy
Stage of disease conducive to sentinel lymph node biopsy as determined by oncologic surgeon
Receiving a planned lymphoscintigraphy procedure
Exclusion Criteria:
History of allergic reactions attributed to compounds of similar chemical or biologic composition to indocyanine green, including those patients with a history of iodide or seafood allergy
Pregnant or breast-feeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yolonda Colson, MD, PhD
Organizational Affiliation
Dana Faber Cancer Institute / Brigham and Women's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Beth Israel Deaconess Medical Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
Facility Name
Brigham and Women's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
Undecided
IPD Sharing Plan Description
At this time, a plan is not in place to make IPD available to other researchers.
Learn more about this trial
NIR-Guided Sentinel Lymph Node Mapping in Melanoma
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