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Contrast-Enhanced Ultrasound Imaging for Diagnosing Recurrent Renal Cell Carcinoma (RCC) Post Ablation

Primary Purpose

Recurrent Renal Cell Carcinoma, Renal Cell Carcinoma

Status
Recruiting
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Sulfur Hexafluoride Lipid Microspheres
Contrast-Enhanced Ultrasound
Computed Tomography
Magnetic Resonance Imaging
Electronic Health Record Review
Sponsored by
Thomas Jefferson University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Recurrent Renal Cell Carcinoma

Eligibility Criteria

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

Inclusion Criteria: Previously received cryotherapy or microwave therapy of RCC Has available contrast enhanced (CE)-MRI or CE-CT imaging prior to ablative therapy Have previously had or are scheduled to have a contrast-enhanced MRI/CT for the monitoring of RCC recurrence within 4 weeks of the CEUS study Be at least 18 years of age Be medically stable If a female of child-bearing age, must have a negative pregnancy test Have signed Informed Consent to participate in the study Exclusion Criteria: Patients who are medically unstable, patients who are seriously or terminally ill, and patients whose clinical course is unpredictable Patients with known sensitivities to the components of Lumason Patients with severe emphysema, pulmonary vasculitis, or a history of pulmonary emboli

Sites / Locations

  • Sidney Kimmel Cancer Center at Thomas Jefferson UniversityRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Diagnostic (CEUS with MRI/CT)

Arm Description

Patients receive Lumason IV and undergo CEUS imaging with MRI/CT on study. Patients' electronic medical record is reviewed every 6 months throughout study.

Outcomes

Primary Outcome Measures

Renal cell carcinoma recurrence
Baseline imaging will be reviewed and compared to the contrast enhanced imaging to diagnose recurrence.

Secondary Outcome Measures

Improvement of diagnostic imaging using 2D contrast-enhanced ultrasound (CEUS) with magnetic resonance/ computed tomography fusion
Contrast-enhanced imaging on all patients will be evaluated by radiologists at each site to determine if it increases the ability to diagnose recurrence compared to standard imaging.
Measurement with multimodality 3D CEUS to improve detection of recurrence
3D CEUS imaging will be evaluated by radiologists at each site to determine if it improved detection of recurrence.

Full Information

First Posted
November 29, 2022
Last Updated
October 19, 2023
Sponsor
Thomas Jefferson University
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1. Study Identification

Unique Protocol Identification Number
NCT05641935
Brief Title
Contrast-Enhanced Ultrasound Imaging for Diagnosing Recurrent Renal Cell Carcinoma (RCC) Post Ablation
Official Title
Multi-Modality Detection of RCC Recurrence Post Ablation
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
November 3, 2022 (Actual)
Primary Completion Date
August 31, 2027 (Anticipated)
Study Completion Date
February 2028 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Thomas Jefferson University

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.
Yes

5. Study Description

Brief Summary
This phase II trial studies how well contrast-enhanced ultrasound (CEUS) works for diagnosing patients with renal cell cancer (RCC) that has come back (recurrent) after an ablation. Diagnostic imaging, such as CEUS, may help find and monitor long term renal cell cancer recurrence following cryo or microwave ablation.
Detailed Description
PRIMARY OBJECTIVE: I. To characterize and compare the sensitivity, specificity, positive and negative predictive value, and inter-reader agreement of 2D contrast-enhanced ultrasound (CEUS) and contrast-enhanced computed tomography (CT)/magnetic resonance imaging (MRI) for detecting recurrent or residual renal cell carcinoma (RCC) following ablation, using a combination of standard of care imaging follow-up and tissue pathology as a reference standard. SECONDARY OBJECTIVES: I. To evaluate the potential improvement to the qualitative assessments of 2D CEUS when fused with the patient's pre-treatment cross sectional imaging. II. To assess the potential added value of using multi-modality volumetric CEUS for detecting RCC recurrence post ablation. III. To explore the use of quantitative imaging parameters extracted from 2D/3D CEUS datasets to determine if this improves the overall performance of CEUS. EXPLORATORY OBJECTIVE: I. An advanced Doppler technique designed for detection of slower flow will also be investigated as a non-contrast based approach for detecting recurrent disease. OUTLINE: Patients receive Lumason intravenously (IV) and undergo CEUS imaging with MRI/CT on study. Patients' electronic medical record is reviewed every 6 months throughout study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Recurrent Renal Cell Carcinoma, Renal Cell Carcinoma

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
210 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Diagnostic (CEUS with MRI/CT)
Arm Type
Experimental
Arm Description
Patients receive Lumason IV and undergo CEUS imaging with MRI/CT on study. Patients' electronic medical record is reviewed every 6 months throughout study.
Intervention Type
Drug
Intervention Name(s)
Sulfur Hexafluoride Lipid Microspheres
Other Intervention Name(s)
Lumason, SF6 Lipid Microspheres, Sulfur Hexafluoride Lipid-type A Microspheres
Intervention Description
Given IV
Intervention Type
Procedure
Intervention Name(s)
Contrast-Enhanced Ultrasound
Other Intervention Name(s)
CEUS
Intervention Description
Undergo CEUS
Intervention Type
Procedure
Intervention Name(s)
Computed Tomography
Other Intervention Name(s)
CAT, CAT Scan, Computed Axial Tomography, computerized axial tomography, Computerized Tomography, CT, CT SCAN, tomography
Intervention Description
Undergo CT
Intervention Type
Procedure
Intervention Name(s)
Magnetic Resonance Imaging
Other Intervention Name(s)
Magnetic Resonance, Magnetic Resonance Imaging Scan, Medical Imaging, Magnetic Resonance / Nuclear Magnetic Resonance, MR, MR Imaging, MRI, MRI Scan, NMR Imaging, NMRI, nuclear magnetic resonance imaging
Intervention Description
Undergo MRI
Intervention Type
Other
Intervention Name(s)
Electronic Health Record Review
Intervention Description
Review electronic medical record
Primary Outcome Measure Information:
Title
Renal cell carcinoma recurrence
Description
Baseline imaging will be reviewed and compared to the contrast enhanced imaging to diagnose recurrence.
Time Frame
Up to 2 years
Secondary Outcome Measure Information:
Title
Improvement of diagnostic imaging using 2D contrast-enhanced ultrasound (CEUS) with magnetic resonance/ computed tomography fusion
Description
Contrast-enhanced imaging on all patients will be evaluated by radiologists at each site to determine if it increases the ability to diagnose recurrence compared to standard imaging.
Time Frame
Up to 2 years
Title
Measurement with multimodality 3D CEUS to improve detection of recurrence
Description
3D CEUS imaging will be evaluated by radiologists at each site to determine if it improved detection of recurrence.
Time Frame
Up to 2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Previously received cryotherapy or microwave therapy of RCC Has available contrast enhanced (CE)-MRI or CE-CT imaging prior to ablative therapy Have previously had or are scheduled to have a contrast-enhanced MRI/CT for the monitoring of RCC recurrence within 4 weeks of the CEUS study Be at least 18 years of age Be medically stable If a female of child-bearing age, must have a negative pregnancy test Have signed Informed Consent to participate in the study Exclusion Criteria: Patients who are medically unstable, patients who are seriously or terminally ill, and patients whose clinical course is unpredictable Patients with known sensitivities to the components of Lumason Patients with severe emphysema, pulmonary vasculitis, or a history of pulmonary emboli
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
John Eisenbrey, PhD
Phone
215-503-5188
Email
john.eisenbrey@jefferson.edu
Facility Information:
Facility Name
Sidney Kimmel Cancer Center at Thomas Jefferson University
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
John Eisenbrey, MD
Email
john.eisenbrey@jefferson.edu

12. IPD Sharing Statement

Learn more about this trial

Contrast-Enhanced Ultrasound Imaging for Diagnosing Recurrent Renal Cell Carcinoma (RCC) Post Ablation

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