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Genomic Profiling of Nodular Thyroid Disease and Thyroid Cancer

Registry for Genomic Profiling of Nodular Thyroid Disease and Thyroid Cancer

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03170804
Enrollment
200
Registered
2017-05-31
Start date
2017-01-01
Completion date
2020-01-01
Last updated
2017-05-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Thymic Carcinoma, Thyroid Cancer, Thyroid Diseases, Thyroid Nodule

Brief summary

The purpose of this registry is to collect uniform genomics-centered data on patients with nodular thyroid disease and cancer in a prospective fashion. After initial clinical evaluation patients with thyroid nodules will undergo standard ultrasonographic evaluation and a needle biopsy of the thyroid (fine needle aspiration (FNA) or core biopsy) as clinically indicated. Biopsy samples will be evaluated cyto-pathologically. A molecular/genomic profiling will be obtained using Thyroseq v2 test. Surgical treatment will be performed as per clinically determined indications. Standard surgical pathology will be processed and reported per the institutional policy and procedures. A molecular/genomic profiling will be obtained using Thyroseq v2 on the surgical specimen. All patients undergoing thyroid nodule work-up may be enrolled. The registry will collect patient demographic and clinical data, cytopathology reports, and surgical pathology reports and slides (if/when a review is required).

Detailed description

This is an open-ended prospective registry. The patients who were diagnosed with thyroid nodules will have a complete clinical and US evaluation. Thyroid nodule biopsy indication and FNA vs core biopsy choices will be made entirely on the clinical grounds, by the managing physicians. Thyroid nodule biopsies may be performed at a participating medical or surgical endocrinology office. Following standard cytologic examination a molecular testing using Thyroseq will be performed. The biopsy results will be categorized according to Bethesda scoring system. Category I is non-diagnostic FNA and will require a repeat FNA. Category II is benign cytology, categories III, IV and V are the indeterminate group, and category VI is malignant cytology. The FNA analysis of registry patients will be collected under six groups. Thyroseq molecular testing may be deferred if not felt needed following cytology. 1. Cytology(benign) / Thyroseq(-) 2. Cytology(benign) / Thyroseq(+) 3. Cytology(indeterminate) / Thyroseq(-) 4. Cytology(indeterminate) / Thyroseq(+) 5. Cytology(Malignant) / Thyroseq(-) 6. Cytology(Malignant) / Thyroseq(+). Thyroid operation indication and lobectomy vs total thyroidectomy choices will be made entirely on the clinical grounds, by the managing physicians. The routine histopathology will be processed and reported as per the institutional protocols. The molecular testing of the preoperatively biopsied and intraoperatively and postoperatively identified lesions will be performed, as indicated. The registry is open to all interested physicians involved in thyroid patient care and interested in participating

Interventions

None listed

Sponsors

Aventura Hospital and Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients will be eligible for registry enrollment if they are undergoing thyroid nodule work-up.

Exclusion criteria

* Patients will not be eligible for registry enrollment if a work-up beyond clinical evaluation is not indicated.

Design outcomes

Primary

MeasureTime frameDescription
prognostic value of Thyroseq v2 molecular/genomic profilingan average of 1 yearThe purpose of this registry is to collect uniform data on patients with nodular thyroid disease and thyroid cancer in a prospective fashion. Data collected will primarily be analyzed for diagnostic and prognostic value of Thyroseq v2 molecular/genomic profiling.

Countries

United States

Contacts

Primary ContactSeza Gulec, MD
sgulec@fiu.edu7866930821

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026