Quantitative Imaging Biomarkers for Sarcoma
Primary Purpose
Sarcoma
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
DCE and DWI MRI
Surgery
Sponsored by
About this trial
This is an interventional diagnostic trial for Sarcoma focused on measuring Dynamic Contrast Enhanced MRI, Diffusion Weighted MRI, Magnetic Resonance Imaging (MRI)
Eligibility Criteria
Inclusion Criteria:
- New diagnosis of de novo sarcoma of all histologies (including soft tissue sarcoma, osteosarcoma, Ewing sarcoma, and chondrosarcoma) confirmed by biopsy
- Scheduled to be treated with surgical resection at the sarcoma or cancer center of participating sites
- Availability of the patient's medical information
- Provide written informed consent for the study
- Eighteen years of age or older
- Ability to remain motionless in MRI scanner for approximately 40 minutes
Exclusion Criteria:
Patients with contra-indications for contrast enhanced MR exam, including:
- Cardiac pacemaker or pacemaker wiring in situ
- Cerebral clips or metal artificial cardiac valves
- Ossicle prosthesis
- Conditions that could produce a dangerous situation in the presence of a strong magnetic field: line metallic implants, shrapnel, inability to lie still, and conditions that can worsen inside confined spaces (severe claustrophobia, psychosis)
- Acute or chronic severe renal disease as determined by glomerular filtration rate (GFR) < 30 ml/min/1.73m2
- Pregnancy or breastfeeding
Sites / Locations
- Columbia University Medical Center
- Huntsman Cancer Institute, University of Utah
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
DCE and DWI MRI group
Arm Description
Patients will undergo a baseline MR exam at enrollment within 4 weeks prior to scheduled surgery, which will include DW-MRI and DCE-MRI prior to surgery and tumor tissue collection.
Outcomes
Primary Outcome Measures
Correlation coefficient of Ktrans (DCE MR parameter) and Apparent Diffusion Coefficient (ADC) (DWI MR parameter) with microvessel density obtained from histopathology.
The primary endpoint of this study is to evaluate the correlation of the estimated in vivo Dynamic Contrast Enhanced and Diffusion weighted MRI parameters with ex vivo histopathologic measurements obtained from tumor tissue. Correlation coefficient (range: -1 to 1).
Secondary Outcome Measures
Full Information
NCT ID
NCT02579980
First Posted
October 15, 2015
Last Updated
March 22, 2019
Sponsor
Columbia University
Collaborators
National Cancer Institute (NCI)
1. Study Identification
Unique Protocol Identification Number
NCT02579980
Brief Title
Quantitative Imaging Biomarkers for Sarcoma
Official Title
Development of Quantitative Imaging Biomarkers for Evaluating Sarcoma Patients
Study Type
Interventional
2. Study Status
Record Verification Date
March 2019
Overall Recruitment Status
Completed
Study Start Date
October 2015 (Actual)
Primary Completion Date
December 2017 (Actual)
Study Completion Date
December 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Columbia University
Collaborators
National Cancer Institute (NCI)
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
Unless a cancer quickly gets smaller with radiation or chemotherapy, the investigators cannot tell if the treatment is working or not. In this research program, two techniques using magnetic resonance imaging (MRI) scanning will be tested in people who have sarcomas, which are rare cancers starting in muscle, tendons, and bones. These particular MRI tests are called dynamic contrast enhanced MRI and diffusion weighted MRI. These MRI scans allow visualization of how sarcomas are different from the normal organs of the body. These MRI tests will tell us the location of sarcoma and its proximity to other structures, as well as correlation of imaging with pathological characteristics after surgery
Detailed Description
Dynamic Contrast Enhanced MRI (DCE-MRI) and Diffusion Weighted MRI (DW-MRI) are imaging approaches that are being utilized in preclinical evaluation as well as clinical trials. DW-MRI is a technique for quantifying the increase in water diffusion caused by cellular necrosis or apoptosis in tumors within days of therapy. DCE-MRI is frequently used in preclinical and early clinical trial assessment of anti-angiogenic and vascular disrupting compounds, also within hours of therapeutic intervention. Evidence of drug efficacy and dose-dependent response has been demonstrated with certain angiogenesis inhibitors. It may also provide useful information for identifying early disease progression, independent of the treatment modality. While these approaches provide additional functional information, they have yet to be validated in sarcoma patients. This study seeks to develop a standardized protocol for performing DCE-MRI and DW-MRI and implement this in a clinical trial of patients with sarcomas who will have surgical resection as part of their standard care. This will allow the accuracy of in vivo MRI measurements to be directly compared to histology as ground truth. The study will also determine the reproducibility of these techniques using repeat baseline imaging as well as evaluate the quantitative changes in these parameters before and after therapy and correlate with histopathology. The collaboration between Columbia University and the University of Utah for this project will allow the existing quantitative MRI approaches to be expanded to a multi-center setting, and will establish a paradigm infrastructure for future expansion to larger scale multi-center therapeutic trials in sarcoma.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sarcoma
Keywords
Dynamic Contrast Enhanced MRI, Diffusion Weighted MRI, Magnetic Resonance Imaging (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
32 (Actual)
8. Arms, Groups, and Interventions
Arm Title
DCE and DWI MRI group
Arm Type
Experimental
Arm Description
Patients will undergo a baseline MR exam at enrollment within 4 weeks prior to scheduled surgery, which will include DW-MRI and DCE-MRI prior to surgery and tumor tissue collection.
Intervention Type
Procedure
Intervention Name(s)
DCE and DWI MRI
Intervention Description
Dynamic Contrast Enhanced MRI (DCE-MRI) and Diffusion Weighted MRI (DW-MRI): DW-MRI is a technique for quantifying the increase in water diffusion caused by cellular necrosis or apoptosis in tumors within days of therapy. DCE-MRI is frequently used in preclinical and early clinical trial assessment of anti-angiogenic and vascular disrupting compounds, also within hours of therapeutic intervention.
Intervention Type
Procedure
Intervention Name(s)
Surgery
Other Intervention Name(s)
Tumor resection
Intervention Description
Standard of care procedure for sarcoma patients
Primary Outcome Measure Information:
Title
Correlation coefficient of Ktrans (DCE MR parameter) and Apparent Diffusion Coefficient (ADC) (DWI MR parameter) with microvessel density obtained from histopathology.
Description
The primary endpoint of this study is to evaluate the correlation of the estimated in vivo Dynamic Contrast Enhanced and Diffusion weighted MRI parameters with ex vivo histopathologic measurements obtained from tumor tissue. Correlation coefficient (range: -1 to 1).
Time Frame
through study completion, an average of 4 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
New diagnosis of de novo sarcoma of all histologies (including soft tissue sarcoma, osteosarcoma, Ewing sarcoma, and chondrosarcoma) confirmed by biopsy
Scheduled to be treated with surgical resection at the sarcoma or cancer center of participating sites
Availability of the patient's medical information
Provide written informed consent for the study
Eighteen years of age or older
Ability to remain motionless in MRI scanner for approximately 40 minutes
Exclusion Criteria:
Patients with contra-indications for contrast enhanced MR exam, including:
Cardiac pacemaker or pacemaker wiring in situ
Cerebral clips or metal artificial cardiac valves
Ossicle prosthesis
Conditions that could produce a dangerous situation in the presence of a strong magnetic field: line metallic implants, shrapnel, inability to lie still, and conditions that can worsen inside confined spaces (severe claustrophobia, psychosis)
Acute or chronic severe renal disease as determined by glomerular filtration rate (GFR) < 30 ml/min/1.73m2
Pregnancy or breastfeeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lawrence H Schwartz, MD
Organizational Affiliation
James Picker Professor and Chairman Department of Radiology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Columbia University Medical Center
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States
Facility Name
Huntsman Cancer Institute, University of Utah
City
Salt Lake City
State/Province
Utah
ZIP/Postal Code
84112
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Links:
URL
http://qibawiki.rsna.org/index.php?title=DCE-MRI_tech_ctte
Description
DCE-MRI Technical Committee. DCE-MRI Quantification Profile, Quantitative Imaging Biomarkers Alliance (QIBA). Version 1.0. Publicly Reviewed Version. QIBA.
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Quantitative Imaging Biomarkers for Sarcoma
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