The Role of Gadoxetate (Eovist) Enhanced CT in Evaluating Cholangiocarcinoma
Primary Purpose
Cholangiocarcinoma
Status
Completed
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
CT scan
Sponsored by
About this trial
This is an interventional treatment trial for Cholangiocarcinoma focused on measuring Cholangiocarcinoma
Eligibility Criteria
Inclusion Criteria:
- Subjects will be adult (age 19 or older) with suspected cholangiocarcinoma of the liver.
- Subject must be able to provide a written informed consent.
- Subject will be scheduled for gadoxetate contrast enhanced MRI scan of the liver (obtained as part of usual clinical practice).
Exclusion Criteria:
- Standard MRI safety screening criteria will be employed, and subject will be excluded if any contraindications to undergo MRI are met.
- Subjects with metallic biliary stents or multiple peripancreatic surgical clips on abdominal MDCT will be excluded.
- Subjects on hemodialysis or with glomerular filtration rate (GFR) less than 30 will be excluded.
- Subjects will not be excluded on the basis of gender, race, ethnicity, or religion.
- Subject may not be pregnant or lactating.
Sites / Locations
- University of Alabama at Birmingham
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
CT imaging
Arm Description
Patients will undergo a standard of care Gadoxetate (Eovist) MRI for cholangiocarcinoma. Patients will then be immediately placed on the CT scanner. Patients will undergo a dual energy CT of the abdomen with no additional contrast.
Outcomes
Primary Outcome Measures
Number of Subjects Where Hilar Cholangiocarcinomas Could be Visualized Using Gadoxetate Disodium Enhanced Dual Energy CT
CT scans were assessed for tumor visualization after use of Gadoxetate disodium
Secondary Outcome Measures
Full Information
NCT ID
NCT01673802
First Posted
August 13, 2012
Last Updated
April 12, 2017
Sponsor
University of Alabama at Birmingham
Collaborators
Society of Abdominal Radiology
1. Study Identification
Unique Protocol Identification Number
NCT01673802
Brief Title
The Role of Gadoxetate (Eovist) Enhanced CT in Evaluating Cholangiocarcinoma
Official Title
The Role of Gadoxetate Enhanced Spectral Dual-Energy CT in Evaluating Hilar Cholangiocarcinoma
Study Type
Interventional
2. Study Status
Record Verification Date
April 2017
Overall Recruitment Status
Completed
Study Start Date
August 2012 (undefined)
Primary Completion Date
January 2014 (Actual)
Study Completion Date
January 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Alabama at Birmingham
Collaborators
Society of Abdominal Radiology
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this project is to evaluate the role of gadoxetate (Eovist®) enhanced dual-energy CT in better evaluating perihilar cholangiocarcinoma. This pilot project aims to address a long-term pitfall in the imaging of cholangiocarcinomas, by providing higher resolution delineation of these often infiltrative tumors on single-source, Dual-Energy Spectral Multi Detector CT (MDCT), capitalizing on improved spatial resolution achievable with MDCT compared to MRI and at the same time producing a non-invasive CT cholangiogram to aid in accurate diagnosis and treatment planning of cholangiocarcinoma, particularly, the hilar variety.
Detailed Description
The purpose of this project is to evaluate the role of gadoxetate (Eovist) enhanced dual-energy CT in better evaluating perihilar cholangiocarcinoma, by exploiting the combination of the physiologic behavior of gadoxetate in liver tissue combined with the advantageous mass attenuation coefficient of Gadolinium achievable through dual energy technique. This combination of unique CT imaging sensitivity, high resolution and differential enhancement potentially allows improved visualization and detection of tumor relative to enhancing surrounding hepatic parenchyma and ductal anatomy in the hepatobiliary phase, due to the biliary excretion of the agent.
Cholangiocarcinoma is a hepatic adenocarcinoma that arises from the bile duct epithelium and is the second most prevalent liver cancer after hepatocellular carcinoma. The hilar intrahepatic variety of cholangiocarcinoma can present as an infiltrative, exophytic, or polypoid lesion. Most extra-hepatic cholangiocarcinomas are infiltrative, causing a focal stricture of the bile duct and result in proximal biliary ductal dilatation.
While magnetic resonance (MR) cholangiography is diagnostic in the majority of patients with malignant hilar strictures, evaluation is limited by spatial resolution and in some patients, the inability to have an MRI scan. Standard Multi Detector CT (MDCT) using iodinated contrast agents, on the other hand, is limited in evaluation of cholangiocarcinomas, due to the lack of consistent enhancement of the tumor with iodinated contrast.
Single-source, Dual-Energy (SSDE) Spectral MDCT utilizes a single fast switching x-ray beam source to acquire near simultaneous data sets at two different photon energies during a single acquisition. Data is acquired at 80 kilovolt peak (kVp) and 140 kVp with image reconstruction achievable as a selectable monochromatic presentation over a range of 40 - 140 kiloelectron volt (keV), typically 70-78 keV for diagnostic image presentation. At lower tube voltage, the frequency of photoelectric interactions increases exponentially and is strongly dependent on the atomic number. Therefore, for substances with higher atomic number, such as iodine and gadolinium the increased frequency of photoelectric and k-edge interactions at low tube voltage substantially increases CT attenuation, thus improving contrast. Gadolinium is further unique with k-edge attenuation at approximately 53 keV, within the available monochromatic reconstruction range, thus allowing for significant greater detectability. Additional material decomposition technique allows for unique material presentation and analysis such as gadolinium/ water pair analysis with high spatial resolution.
Dual-Energy technology is limited by the types of contrast agents currently available, all based on Iodine. Gadoxetate (Eovist) is a relatively new Gadolinium based MRI contrast agent that is capable of producing not only standard appearing MRI images in the hepatic arterial and portal venous phases, but also provides an opportunity to better visualize the bile ducts and liver parenchyma as it is excreted by the liver into the biliary system during the hepatobiliary phase.
This pilot project aims to address a long-term pitfall in the imaging of cholangiocarcinomas, by providing higher resolution delineation of these often infiltrative tumors on single-source, Dual-Energy Spectral MDCT, capitalizing on improved spatial resolution achievable with MDCT compared to MRI and at the same time producing a non-invasive CT cholangiogram to aid in accurate diagnosis and treatment planning of cholangiocarcinoma, particularly, the hilar variety.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cholangiocarcinoma
Keywords
Cholangiocarcinoma
7. Study Design
Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Single Group Assignment
Model Description
Single arm study, with dose adjustment.
Masking
None (Open Label)
Allocation
N/A
Enrollment
18 (Actual)
8. Arms, Groups, and Interventions
Arm Title
CT imaging
Arm Type
Experimental
Arm Description
Patients will undergo a standard of care Gadoxetate (Eovist) MRI for cholangiocarcinoma. Patients will then be immediately placed on the CT scanner. Patients will undergo a dual energy CT of the abdomen with no additional contrast.
Intervention Type
Drug
Intervention Name(s)
CT scan
Other Intervention Name(s)
Dual Energy CT
Intervention Description
Gadoxetate (Eovist) enhanced dual energy CT
Primary Outcome Measure Information:
Title
Number of Subjects Where Hilar Cholangiocarcinomas Could be Visualized Using Gadoxetate Disodium Enhanced Dual Energy CT
Description
CT scans were assessed for tumor visualization after use of Gadoxetate disodium
Time Frame
24 hrs
10. Eligibility
Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Subjects will be adult (age 19 or older) with suspected cholangiocarcinoma of the liver.
Subject must be able to provide a written informed consent.
Subject will be scheduled for gadoxetate contrast enhanced MRI scan of the liver (obtained as part of usual clinical practice).
Exclusion Criteria:
Standard MRI safety screening criteria will be employed, and subject will be excluded if any contraindications to undergo MRI are met.
Subjects with metallic biliary stents or multiple peripancreatic surgical clips on abdominal MDCT will be excluded.
Subjects on hemodialysis or with glomerular filtration rate (GFR) less than 30 will be excluded.
Subjects will not be excluded on the basis of gender, race, ethnicity, or religion.
Subject may not be pregnant or lactating.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John V Thomas, MD
Organizational Affiliation
University of Alabama at Birmingham
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Alabama at Birmingham
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35294
Country
United States
12. IPD Sharing Statement
Learn more about this trial
The Role of Gadoxetate (Eovist) Enhanced CT in Evaluating Cholangiocarcinoma
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