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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05575440
Other study ID # 20-010573
Secondary ID NCI-2022-03071
Status Recruiting
Phase
First received
Last updated
Start date April 22, 2022
Est. completion date May 1, 2026

Study information

Verified date October 2023
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Description:

PRIMARY OBJECTIVES: I. 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. II. 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 24
Est. completion date May 1, 2026
Est. primary completion date May 1, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Computed Tomography
Undergo a PET/CT scan
Radiation:
Fluorine F 18 Tetrafluoroborate
Given IV
Procedure:
Positron Emission Tomography
Undergo a PET/CT scan
Other:
Survey Administration
Ancillary studies

Locations

Country Name City State
United States Mayo Clinic in Rochester Rochester Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Descriptive summaries of detected lesions 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. Up to 2 years
Primary Conspicuities and diagnostic confidence scores for a given lesion 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. Up to 2 years
Secondary True positive and negative lesions 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. Up to 2 years
Secondary Impact of PET on clinical management in differentiated thyroid cancer (DTC) patients 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. Up to 2 years
Secondary Inter-reader reproducibility 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. Up to 2 years
See also
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Terminated NCT03506048 - Lenvatinib and Iodine Therapy in Treating Patients With Radioactive Iodine-Sensitive Differentiated Thyroid Cancer Phase 2
Recruiting NCT04759911 - Selpercatinib Before Surgery for the Treatment of RET-Altered Thyroid Cancer Phase 2
Active, not recruiting NCT03914300 - Testing the Combination of Cabozantinib, Nivolumab, and Ipilimumab (CaboNivoIpi) for Advanced Differentiated Thyroid Cancer Phase 2
Recruiting NCT05003856 - Radiofrequency Ablation for the Treatment of Benign or Low Risk Thyroid Nodule N/A

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