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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorMayo Clinic

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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)

Disqualifiers

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

Trial population

Subjects have biopsy-proven papillary or follicular thyroid cancer and is clinically indicated for 123I-single-photon emission computerized tomography (I-SPECT)/CT total body iodine (TBI) scan

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Computed Tomography

    Procedure/Surgery

    Undergo a PET/CT scan

  • Fluorine F 18 Tetrafluoroborate

    Radiation

    Given IV

  • Positron Emission Tomography

    Procedure/Surgery

    Undergo a PET/CT scan

  • Survey Administration

    Other intervention

    Ancillary studies

Treatment groups

24 Participants
are divided into 1 treatment group
Group A: Observational (18F-TFB PET/CT)4 interventions

Trial outcomes

Primary outcomes

1

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.

Time frame
Up to 2 years
2

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.

Time frame
Up to 2 years

Secondary outcomes

1

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.

Time frame
Up to 2 years
2

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.

Time frame
Up to 2 years
3

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.

Time frame
Up to 2 years

Other outcomes

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