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High-resolution Magnetic Resonance Imaging (MRI) Scans to Look for Spread of Melanoma to Nearby Lymph Nodes

Primary Purpose

Melanoma

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
High-resolution contrast-enhanced MRI scan
Sponsored by
Redwood Regional Medical Group
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Melanoma focused on measuring melanoma, lymph nodes, magnetic resonance imaging, screening, detection

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • history of invasive cutaneous melanoma stages 1-3 within 2 years of treatment of the melanoma by primary excision
  • eligible whether or not a sentinel lymph node biopsy or regional lymph node dissection has been performed
  • adequate renal function (creatinine 2 or less)
  • life expectancy 2 years of more

Exclusion Criteria:

  • history of severe claustrophobia precluding MRI scans
  • known hypersensitivity or other contraindication to gadolinium contrast
  • known presence of metastatic melanoma at sites beyond regional lymph nodes (stage 4)

Sites / Locations

  • Redwood Regional Medical Group

Outcomes

Primary Outcome Measures

Assessment of the sensitivity and specificity of high-resolution MRI scans of regional lymph nodes compared to results from regional lymph node biopsy.

Secondary Outcome Measures

Full Information

First Posted
April 19, 2007
Last Updated
November 8, 2014
Sponsor
Redwood Regional Medical Group
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1. Study Identification

Unique Protocol Identification Number
NCT00463892
Brief Title
High-resolution Magnetic Resonance Imaging (MRI) Scans to Look for Spread of Melanoma to Nearby Lymph Nodes
Official Title
A Phase II Study of High-resolution Contrast-enhanced MRI of Regional Lymph Nodes in Patients With Clinically Localized Invasive Melanoma
Study Type
Interventional

2. Study Status

Record Verification Date
November 2014
Overall Recruitment Status
Completed
Study Start Date
June 2007 (undefined)
Primary Completion Date
November 2011 (Actual)
Study Completion Date
June 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Redwood Regional Medical Group

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The study is designed to see if a high-resolution MRI scan of lymph node areas near where a melanoma has been removed from the skin can pick up the spread of melanoma to those lymph nodes with a high degree of accuracy.
Detailed Description
When a melanoma of the skin is diagnosed, there is some chance it can spread to nearby lymph nodes, and from there to other parts of the body. Currently, patients with melanoma at low risk for spreading to lymph nodes do not get the lymph nodes assessed except by a physical exam. Those at high risk for spreading to lymph nodes get one or more lymph nodes removed surgically to check for melanoma spread. But physical exam alone will often miss small areas of melanoma in lymph nodes; removal of lymph nodes by surgery is painful and can cause complications. Neither assessment tool is optimal. This study is designed to see if use of very high-resolution contrast-enhanced MRI scans of lymph node areas near the primary melanoma site in the skin can accurately detect small areas of melanoma spread to those lymph nodes. If this turns out to be the case, in the future, MRI scans could potentially be an alternative for assessing lymph nodes, compared to physical exams alone or surgical removal of the lymph nodes. In this study, patients with low risk melanoma will receive very high-resolution MRI scans of nearby lymph nodes every 6 months for 5 years of follow-up. If the MRI looks abnormal, the lymph nodes will be biopsied, and results from the biopsy compared to the results from the MRI. Patients with high risk melanoma will get a baseline MRI of the nearby lymph nodes, and then one or more lymph nodes will be removed (usually by sentinel lymph node biopsy) regardless of the MRI results. Again, results from the biopsy will be compared to the results from the MRI. MRI's will still be repeated every 6 months to assess whether lymph nodes not removed at surgery develop any changes. We plan to enroll 200 patients on this study and by the end of the study will have a measure of the sensitivity and specificity of high-resolution MRI scans in the detection of melanoma involvement of regional lymph nodes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Melanoma
Keywords
melanoma, lymph nodes, magnetic resonance imaging, screening, detection

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Procedure
Intervention Name(s)
High-resolution contrast-enhanced MRI scan
Intervention Description
High-resolution contrast-enhanced MRI scan of regional lymph nodes every 6 months on study
Primary Outcome Measure Information:
Title
Assessment of the sensitivity and specificity of high-resolution MRI scans of regional lymph nodes compared to results from regional lymph node biopsy.
Time Frame
5 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: history of invasive cutaneous melanoma stages 1-3 within 2 years of treatment of the melanoma by primary excision eligible whether or not a sentinel lymph node biopsy or regional lymph node dissection has been performed adequate renal function (creatinine 2 or less) life expectancy 2 years of more Exclusion Criteria: history of severe claustrophobia precluding MRI scans known hypersensitivity or other contraindication to gadolinium contrast known presence of metastatic melanoma at sites beyond regional lymph nodes (stage 4)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter Brett, M.D.
Organizational Affiliation
Redwood Regional Medical Group
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
David Feinberg, M.D., Ph.D.
Organizational Affiliation
Redwood Regional Medical Group
Official's Role
Principal Investigator
Facility Information:
Facility Name
Redwood Regional Medical Group
City
Sebastopol
State/Province
California
ZIP/Postal Code
95472
Country
United States

12. IPD Sharing Statement

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High-resolution Magnetic Resonance Imaging (MRI) Scans to Look for Spread of Melanoma to Nearby Lymph Nodes

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