Evaluation of 18F-TFB PET/CT Scan in Patients With Differentiated Thyroid Cancer

Sponsor
Mayo Clinic (Other)
Overall Status
Recruiting
CT.gov ID
NCT05575440
Collaborator
(none)
24
1
36.3
0.7

Study Details

Study Description

Brief Summary

This phase II study evaluates F-18 tetrafluoroborate (18F-TFB) PET/CT scan in patients with differentiated thyroid cancer. Diagnostic imaging is necessary for planning treatment, monitoring therapy response, and identifying sites of recurrent or metastatic disease in differentiated thyroid cancer. 18F-TFB PET/CT may accurately detect recurrent and metastatic thyroid cancer lesions, with the potential to provide information for patient management that is better than the current standard of care imaging practices.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Computed Tomography
  • Radiation: Fluorine F 18 Tetrafluoroborate
  • Procedure: Positron Emission Tomography
  • Other: Survey Administration

Detailed Description

PRIMARY OBJECTIVES:
  1. Evaluate fluorine F 18 tetrafluoroborate (18F-TFB) positron emission tomography (PET)/computed tomography (CT) imaging in patients with intermediate or high risk differentiated thyroid cancer (DTC) and compare to the current clinical standard.

  2. Assess the impact of 18F-TFB PET/CT on clinical management.

OUTLINE:

Patients receive fluorine F 18 tetrafluoroborate intravenously (IV) and undergo PET/CT scan on study.

Study Design

Study Type:
Observational
Anticipated Enrollment :
24 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Evaluation of F-18 Tetrafluoroborate (18F-TFB) PET/CT in Patients With Differentiated Thyroid Cancer
Actual Study Start Date :
Apr 22, 2022
Anticipated Primary Completion Date :
May 1, 2024
Anticipated Study Completion Date :
May 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Observational (18F-TFB PET/CT)

Patients receive fluorine F18 tetrafluoroborate IV and undergo PET/CT scan on study.

Procedure: Computed Tomography
Undergo a PET/CT scan
Other Names:
  • CAT
  • CAT Scan
  • Computed Axial Tomography
  • Computerized Axial Tomography
  • Computerized Tomography
  • CT
  • CT Scan
  • tomography
  • Radiation: Fluorine F 18 Tetrafluoroborate
    Given IV
    Other Names:
  • 18F-Tetrafluoroborate
  • 18F-TFB
  • Procedure: Positron Emission Tomography
    Undergo a PET/CT scan
    Other Names:
  • Medical Imaging, Positron Emission Tomography
  • PET
  • PET Scan
  • Positron Emission Tomography Scan
  • Positron-Emission Tomography
  • proton magnetic resonance spectroscopic imaging
  • Other: Survey Administration
    Ancillary studies

    Outcome Measures

    Primary Outcome Measures

    1. Descriptive summaries of detected lesions [Up to 2 years]

      Descriptive summaries of detected lesions (presence/absence) will include counts and proportions at the patient and lesion level. Overall concordance of these measures across modalities will be estimated using Cohen's kappa with 95% confidence intervals generated by clustered bootstrapping. Per-lesion analysis of detection rates by modality will be performed using cluster-adjusted McNemar's test, accounting for the paired nature of the data (i.e., two scans) and potential within-sample correlation for patients with multiple lesions.

    2. Conspicuities and diagnostic confidence scores for a given lesion [Up to 2 years]

      Conspicuities and diagnostic confidence scores for a given lesion will be averaged across readers. Descriptive summaries of these scores will include medians and interquartile ranges. Concordance of these measures across modality will be evaluated using Lin's concordance correlation coefficient with 95% confidence intervals generated by clustered bootstrapping. Differences in conspicuities and diagnostic confidence scores will be tested using cluster-adjusted Wilcoxon signed-rank tests.

    Secondary Outcome Measures

    1. True positive and negative lesions [Up to 2 years]

      Given true positive and negative lesions determined by histopathology and/or imaging, clinical and laboratory follow-up, we will estimate sensitivity, specificity, net present value, and positive predictive value on a per-lesion and patient basis for 18F TFB PET/CT and 123I single-photon emission computerized tomography/CT along with the corresponding two-sided 95% confidence intervals. The confidence intervals will be constructed using clustered bootstrapping.

    2. Impact of PET on clinical management in differentiated thyroid cancer (DTC) patients [Up to 2 years]

      The impact of PET on clinical management in DTC patients will be evaluated using descriptive statistics. Evidence of discordance among the modalities will be assessed using a McNemar- Bowker test of symmetry.

    3. Inter-reader reproducibility [Up to 2 years]

      Inter-reader reproducibility will be assessed for positivity at the patient level and region level (nominal) as well as standardized uptake values (SUVs) for positive lesions (quantitative). Reproducibility will be reported using the Fleiss' Kappa test for multiple readers for positivity and Pearson intra-class correlation for SUVs.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Subject has biopsy-proven papillary or follicular thyroid cancer

    • Subject is clinically indicated for 123I-SPECT/CT total body iodine (TBI) scan

    • Subject agrees to undergo 18F-TFB PET/CT scan following TBI scan

    • Karnofsky performance status of >= 50 (or Eastern Cooperative Oncology Group [ECOG]/World Health Organization [WHO] equivalent)

    • Subject is able to be scanned - able to lie still on SPECT/CT and PET/CT scanner table for up to 65 minutes (min)

    • Age 18 or older

    • Ability to understand a written informed consent document, and the willingness to sign it

    • Subject is not pregnant

    Exclusion Criteria:
    • Contrast-enhanced CT within 4 last weeks

    • Amiodarone within last 4 months

    • Ingested iodine, kelp tablets, Lugols iodine, or potassium iodide (SSKI) within 2 weeks

    • Unable to lie flat, still or tolerate a PET scan

    • Applied betadine, iodoform, or quick tanning products to skin within last two weeks

    • If using medication withdrawal for stimulation, then exclude if thyroid stimulating hormone (TSH) level < 25

    • Taken anti-thyroid medication within 1 week

    • Subject is breastfeeding

    • Positive pregnancy test

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Mayo Clinic in Rochester Rochester Minnesota United States 55905

    Sponsors and Collaborators

    • Mayo Clinic

    Investigators

    • Principal Investigator: Stephen Broski, Mayo Clinic in Rochester

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Mayo Clinic
    ClinicalTrials.gov Identifier:
    NCT05575440
    Other Study ID Numbers:
    • 20-010573
    • NCI-2022-03071
    First Posted:
    Oct 12, 2022
    Last Update Posted:
    Jan 6, 2023
    Last Verified:
    Nov 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 6, 2023