Dynamic Contrast Enhancement Computed Tomography for Evaluating Tumor Perfusion in Patients With Metastatic Renal Cell Carcinoma Receiving Targeted Therapies: Renal Cell Carcinoma (RCC) Scramble
Primary Purpose
Renal Cell Carcinoma
Status
Active
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Perfusion CT scan
Sponsored by
About this trial
This is an interventional diagnostic trial for Renal Cell Carcinoma focused on measuring RCC, Kidney cancer, Metastatic renal cell carcinoma, mRCC, Dynamic contrast enhanced CT, DCE-CT, Tumor perfusion
Eligibility Criteria
Inclusion Criteria:
- Patient must be enrolled or being considered for enrollment on protocol 2010-0085.
- Patients must have metastatic renal cell carcinoma (RCC).
- Age >/= 18 years.
- Subjects must have adequate renal function as defined by serum creatinine < 1.5x upper limit of normal.
Exclusion Criteria:
- Radiotherapy: Subjects may not have received prior radiotherapy to the index lesion within 4 weeks
- Female subjects who are pregnant or lactating.
- Female subjects of childbearing potential (unless they have a negative serum or urine pregnancy test within 3 days prior to start of study treatment).
- Allergy to CT contrast media requiring the administration of steroid prophylaxis.
Sites / Locations
- University of Texas MD Anderson Cancer Center
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
DCE-CT Scans
Arm Description
DCE-CT = Dynamic contrast enhanced CT - DCE-CT scans 4 weeks prior to and 8 weeks after starting treatment on study 2010-0085.
Outcomes
Primary Outcome Measures
Tumor Blood Flow (BF) Reduction
Changes in perfusion parameters assessed at first re-staging (approximately 8 weeks) and shortly after initiating therapy (2 - 7 days), for three different therapies using organ-directed DCE-CT tumor assessments. Tumor BF of index lesions computed using commercially available software (GE CT perfusion) using the same index lesion assessed on follow-up scans.
Secondary Outcome Measures
Progression Free Survival (PFS)
PFS is calculated from the start of the study until disease progression.
Full Information
NCT ID
NCT01224288
First Posted
October 18, 2010
Last Updated
June 5, 2023
Sponsor
M.D. Anderson Cancer Center
1. Study Identification
Unique Protocol Identification Number
NCT01224288
Brief Title
Dynamic Contrast Enhancement Computed Tomography for Evaluating Tumor Perfusion in Patients With Metastatic Renal Cell Carcinoma Receiving Targeted Therapies: Renal Cell Carcinoma (RCC) Scramble
Official Title
Dynamic Contrast Enhancement Computed Tomography for Evaluating Tumor Perfusion in Patients With Metastatic Renal Cell Carcinoma Receiving Targeted Therapies: Companion to Protocol 2010-0085
Study Type
Interventional
2. Study Status
Record Verification Date
June 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 2011 (Actual)
Primary Completion Date
April 30, 2025 (Anticipated)
Study Completion Date
April 30, 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
M.D. Anderson Cancer Center
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This is a companion protocol to MD Anderson Cancer Center study 2010-0085 (Sequential Therapy in Advanced Renal Cell Carcinoma Therapy: The "START" Trial).
The goal of this clinical research study is to learn if dynamic contrast enhanced computed tomography (DCE-CT) scans can help researchers learn if the study drug received as part of study 2010-0085 (either everolimus, bevacizumab, or pazopanib) is working.
Detailed Description
To perform a DCE-CT scan, a small amount of a special dye (called "CT contrast medium") is injected by vein into the body. Several CT images are then taken over a few minutes to learn how much dye spreads outside of the tumor. This can show how much blood flows to and from the tumor. By performing DCE-CT scans after several weeks on treatment, researchers may learn if changes in blood flow may be a sign that the treatment is working.
Study Procedures:
If you are found to be eligible to take part in this study, you will have a DCE-CT scan to check the status of the disease at the following times:
Within about 4 weeks before you begin treatment on study 2010-0085.
Eight (8) weeks after starting treatment on study 2010-0085.
Before each of the DCE-CT scans are performed, blood (about 1 tablespoon) will be drawn to check your kidney function.
If your doctor thinks it is needed, you will also have a standard-of-care CT scan at these timepoints to check the status of the disease.
Length of Study:
Your participation in this study will be over after the scan(s) 8 weeks after starting treatment on study 2010-0085. You will be taken off of this study if you leave the 2010-0085 study early.
This is an investigational study. The DCE-CT scan is commercially available. Using DCE-CT scans to check the status of kidney cancer is investigational.
Up to 120 patients will take part in this study. All will be enrolled at MD Anderson.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Renal Cell Carcinoma
Keywords
RCC, Kidney cancer, Metastatic renal cell carcinoma, mRCC, Dynamic contrast enhanced CT, DCE-CT, Tumor perfusion
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
120 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
DCE-CT Scans
Arm Type
Experimental
Arm Description
DCE-CT = Dynamic contrast enhanced CT - DCE-CT scans 4 weeks prior to and 8 weeks after starting treatment on study 2010-0085.
Intervention Type
Procedure
Intervention Name(s)
Perfusion CT scan
Intervention Description
DCE-CT scans 4 weeks prior to and 8 weeks after starting treatment on study 2010-0085.
Primary Outcome Measure Information:
Title
Tumor Blood Flow (BF) Reduction
Description
Changes in perfusion parameters assessed at first re-staging (approximately 8 weeks) and shortly after initiating therapy (2 - 7 days), for three different therapies using organ-directed DCE-CT tumor assessments. Tumor BF of index lesions computed using commercially available software (GE CT perfusion) using the same index lesion assessed on follow-up scans.
Time Frame
From 4 weeks prior to first dose to 8 weeks post treatment
Secondary Outcome Measure Information:
Title
Progression Free Survival (PFS)
Description
PFS is calculated from the start of the study until disease progression.
Time Frame
3 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient must be enrolled or being considered for enrollment on protocol 2010-0085.
Patients must have metastatic renal cell carcinoma (RCC).
Age >/= 18 years.
Subjects must have adequate renal function as defined by serum creatinine < 1.5x upper limit of normal.
Exclusion Criteria:
Radiotherapy: Subjects may not have received prior radiotherapy to the index lesion within 4 weeks
Female subjects who are pregnant or lactating.
Female subjects of childbearing potential (unless they have a negative serum or urine pregnancy test within 3 days prior to start of study treatment).
Allergy to CT contrast media requiring the administration of steroid prophylaxis.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chaan Ng, MD
Organizational Affiliation
M.D. Anderson Cancer Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Texas MD Anderson Cancer Center
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
12. IPD Sharing Statement
Links:
URL
http://www.mdanderson.org
Description
University of Texas MD Anderson Cancer Center Website
Learn more about this trial
Dynamic Contrast Enhancement Computed Tomography for Evaluating Tumor Perfusion in Patients With Metastatic Renal Cell Carcinoma Receiving Targeted Therapies: Renal Cell Carcinoma (RCC) Scramble
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