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

Sponsor
Thomas Jefferson University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05641935
Collaborator
(none)
210
1
1
62.9
3.3

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Drug: Sulfur Hexafluoride Lipid Microspheres
  • Procedure: Contrast-Enhanced Ultrasound
  • Procedure: Computed Tomography
  • Procedure: Magnetic Resonance Imaging
  • Other: Electronic Health Record Review
Phase 2

Detailed Description

PRIMARY OBJECTIVE:
  1. 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:
  1. To evaluate the potential improvement to the qualitative assessments of 2D CEUS when fused with the patient's pre-treatment cross sectional imaging.

  2. To assess the potential added value of using multi-modality volumetric CEUS for detecting RCC recurrence post ablation.

  3. 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:
  1. 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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
210 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Multi-Modality Detection of RCC Recurrence Post Ablation
Actual Study Start Date :
Nov 3, 2022
Anticipated Primary Completion Date :
Aug 31, 2027
Anticipated Study Completion Date :
Feb 1, 2028

Arms and Interventions

Arm Intervention/Treatment
Experimental: Diagnostic (CEUS with MRI/CT)

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

Drug: Sulfur Hexafluoride Lipid Microspheres
Given IV
Other Names:
  • Lumason
  • SF6 Lipid Microspheres
  • Sulfur Hexafluoride Lipid-type A Microspheres
  • Procedure: Contrast-Enhanced Ultrasound
    Undergo CEUS
    Other Names:
  • CEUS
  • Procedure: Computed Tomography
    Undergo CT
    Other Names:
  • CAT
  • CAT Scan
  • Computed Axial Tomography
  • computerized axial tomography
  • Computerized Tomography
  • CT
  • CT SCAN
  • tomography
  • Procedure: Magnetic Resonance Imaging
    Undergo MRI
    Other Names:
  • 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
  • Other: Electronic Health Record Review
    Review electronic medical record

    Outcome Measures

    Primary Outcome Measures

    1. Renal cell carcinoma recurrence [Up to 2 years]

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

    Secondary Outcome Measures

    1. Improvement of diagnostic imaging using 2D contrast-enhanced ultrasound (CEUS) with magnetic resonance/ computed tomography fusion [Up to 2 years]

      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.

    2. Measurement with multimodality 3D CEUS to improve detection of recurrence [Up to 2 years]

      3D CEUS imaging will be evaluated by radiologists at each site to determine if it improved detection of recurrence.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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 2 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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Sidney Kimmel Cancer Center at Thomas Jefferson University Philadelphia Pennsylvania United States 19107

    Sponsors and Collaborators

    • Thomas Jefferson University

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Thomas Jefferson University
    ClinicalTrials.gov Identifier:
    NCT05641935
    Other Study ID Numbers:
    • 22F.825
    First Posted:
    Dec 8, 2022
    Last Update Posted:
    Dec 8, 2022
    Last Verified:
    Nov 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 8, 2022