About this trial
The purpose of this study is to determine whether results from a fine needle biopsy are the same as results from a larger sample that is acquired from the surgical pathology using the Thyroid GuidePx® test in patients with papillary thyroid carcinoma.
Eligibility criteria
Qualifiers
Age ≥ 18 years
A diagnosis of papillary thyroid cancer based on a fine needle biopsy (FNB) interpreted as a Bethesda V or VI cytology
A diagnosis of Atypia of Undetermined Significance (AUS) or Follicular Lesion of Undetermined Significance (FLUS) interpreted as Bethesda III or IV cytology (indeterminate nodule) ThyroSpec positive for BRAFV600E, TERT, rearrangements in BRAF, RET, NTRK1, NTRK3, RAS + TERT, RAS + EIF1AX, AKT1, PI3CA, CTNNB1, EGFR, rearrangements in ALK
Tumor size > 1 cm in maximal diameter on imaging prior to surgery
Disqualifiers
History of radiation to the neck for situations such as medical radiation, radiation exposure in a work environment (nuclear power plant/reactor), or radiation exposure through release of radioactive materials into the nearby environment from a nuclear power plant/reactor.
Unable or unwilling to have a fine needle biopsy
Unwilling to undergo thyroidectomy
Final pathology does not demonstrate papillary thyroid cancer
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Sponsors and collaborators
University of Calgary
Lead sponsor
Qualisure Diagnostics Inc.
Collaborator
Alberta Health services
Collaborator