A retrospective analysis of molecular testing in cytologically indeterminate thyroid nodules with histologic correlation: Experience at a heterogenous multihospital system

Author:

Sura Gloria H.12ORCID,Thrall Michael J.1ORCID,Rogers John1,Hodjat Parsa1,Christensen Paul1,Cubb Trisha D.3,Khadra Helmi S.4,Thomas Jessica S.1,Jacobi Elizabeth M.1ORCID

Affiliation:

1. Department of Pathology and Genomic Medicine Houston Methodist Hospital Houston Texas USA

2. Department of Pathology and Laboratory Medicine The University of Texas MD Anderson Cancer Center Houston Texas USA

3. Department of Endocrinology Houston Methodist Hospital Houston Texas USA

4. Department of Surgery Houston Methodist Hospital Houston Texas USA

Abstract

AbstractIntroductionThyroid malignancy is one of the most common types of cancer in developed nations. Currently, fine‐needle aspiration cytology (FNAC) is the most practical screening test for thyroid nodules. However, cytologically indeterminate samples comprise approximately 15%–30% of cases. These include cases classified as atypia of undetermined significance (AUS), follicular neoplasm (FN), and suspicious for malignancy (SFM). Indeterminate cases can be sent for molecular testing for more definitive classification to help guide management and prevent overtreatment of benign thyroid nodules. We conducted a retrospective review on molecular testing of indeterminate thyroid FNAC and reviewed subsequent histologic diagnoses in resection specimens to assess how molecular testing supported a diagnosis and its effect on clinical management of patients at our institution.MethodsA retrospective chart review was performed on all thyroid FNAC specimens, corresponding molecular testing, and subsequent surgical resection specimens over a 6‐year period.ResultsA total of 10,253 thyroid FNAC were performed in our hospital system during our study period, of which 10% (n = 1102/10,253) had indeterminate FNAC results. Molecular testing was performed in 16% (n = 178/1102) of indeterminate cytology cases. Genetic alterations were identified in 39% (n = 69/178) of the cases sent for molecular testing. The majority of cytologically indeterminate cases sent for molecular testing were follicular‐patterned lesions and their corresponding resection specimens revealed mostly low grade follicular derived neoplasms (i.e., follicular adenoma, non‐invasive follicular thyroid neoplasm with papillary‐like nuclear features, and follicular variant of papillary thyroid carcinoma). Of the cases with identified genetic alterations, 75% (n = 52/69) were treated surgically. In cases with no genetic alterations identified, only 18% (n = 20/109) were treated surgically.Discussion/ConclusionMolecular testing on cytologically indeterminate thyroid nodules can help provide a more accurate risk of malignancy assessment in patients with lesions that are difficult to diagnosis based solely on FNAC morphology. The types of genetic alterations identified in the resected thyroid lesions were consistent with what has been previously described in the literature. Additionally, we found that in the patients with indeterminate thyroid FNAC with adjunct molecular testing, more than half did not undergo surgical resection. This finding emphasizes the value of adding molecular testing in patients, particularly when attempting to reduce unnecessary surgical intervention.

Publisher

Wiley

Subject

General Medicine,Histology,Pathology and Forensic Medicine

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