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Spots Global Cancer Trial Database for Randomized Trial Comparing Performance of Molecular Markers for Indeterminate Thyroid Nodules

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Trial Identification

Brief Title: Randomized Trial Comparing Performance of Molecular Markers for Indeterminate Thyroid Nodules

Official Title: Randomized Trial Comparing Performance of Molecular Markers for Indeterminate Thyroid Nodules

Study ID: NCT02681328

Conditions

Thyroid

Study Description

Brief Summary: The purpose of this study is to compare the performance of Afirma GSC and ThyroSeq v.3 in indeterminate thyroid nodules to determine which test can allow more patients to avoid unnecessary surgery and preserve quality of life. In the initial phase of this study, the performance of Afirma GEC and ThyroSeq v.2 were compared.

Detailed Description: 1. All patients undergoing thyroid FNA within the UCLA Health System will be randomized at the time of FNA to a single molecular test (GSC or ThyroSeq v.3). In the previous phase of the study, patients were randomized to the previous versions of a single molecular test (GEC or ThyroSeq v.2). 2. During the FNA, a sample will be collected for the molecular test. 3. If the cytology results are indeterminate (Bethesda categories 3 or 4), the molecular test will be reflexively sent off. 4. We will help patients with indeterminate thyroid nodules to establish care with an endocrinologist, if they do not already have one. The physicians will make treatment recommendations using best practices and incorporating the results of the molecular test. We anticipate that most patients with a positive molecular test will undergo surgery, while the majority with a negative test will be surveiled. 5. Patients who undergo surgery will have histopathologic evaluation of the thyroid, which will determine whether the index thyroid nodule was benign or malignant. 6. Patients who do not undergo surgery will have a followup ultrasound at 6 and 12 months, or sooner at the discretion of the treating physician. 7. We will assess thyroid-specific quality of life at baseline (following initial diagnosis of an indeterminate thyroid nodule) and during followup (at 6 and 12 months) using the short version of Thyroid-Related Patient-Reported Outcome.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Jonsson Comprehensive Cancer Center at UCLA, Los Angeles, California, United States

Contact Details

Name: Masha Livhits, MC

Affiliation: Visiting Assistant Professor

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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