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Clinical use of Molecular Data in Thyroid Nodules and Cancer

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ENDOCRINE SOC
DOI: 10.1210/clinem/dgad282

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thyroid cancer; differentiated thyroid cancer; mutations; gene; molecular testing; targeted therapy

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Advancements in molecular genetics have led to diagnostic tests, prognostic markers, and therapeutic agents for thyroid cancer. Genetic alterations in MAPK and PI3K/Akt pathways play a key role in differentiated thyroid cancer. Molecular tests like ThyroSeq v.3, Afirma Gene Sequencing Classifier, and ThyGeNEXT/ThyraMIR have been developed for diagnosing indeterminate thyroid nodules. They have high sensitivities and negative predictive values, reducing unnecessary surgeries. Molecular testing is also important for targeted therapy options and managing advanced disease.
Over the past 3 decades, advances in the molecular genetics of thyroid cancer (TC) have been translated into diagnostic tests, prognostic markers, and therapeutic agents. The main drivers in differentiated TC pathogenesis are single-point mutations and gene fusions in components of the Mitogen-activated protein kinase (MAPK) and phosphoinositide-3-kinase-protein kinase B/Akt (PI3K/Akt) pathways. Other important genetic alterations in the more advanced types of TC include TERT promoter, TP53, EIF1AX, and epigenetic alterations. Using this knowledge, several molecular tests have been developed for cytologically indeterminate thyroid nodules. Currently, 3 commercially available tests are in use including a DNA/RNA-based test (ThyroSeq v.3), an RNA-based test (Afirma Gene Sequencing Classifier), and a hybrid DNA/miRNA test, ThyGeNEXT/ThyraMIR. These tests are mostly used to rule out malignancy in Bethesda III and IV thyroid nodules because they all have high sensitivities and negative predictive values. Their common use, predominantly in the United States, has resulted in a significant reduction in unnecessary thyroid surgeries for benign nodules. Some of these tests also provide information on the underlying molecular drivers of TC; this may support decision making in initial TC management planning, although this practice has not yet been widely adopted. More importantly, molecular testing is essential in patients with advanced disease before using specific mono-kinase inhibitors (eg, selpercatinib for RET-altered TC) because these drugs are ineffective in the absence of a specific molecular target. This mini-review discusses the utilization of molecular data in the clinical management of patients with thyroid nodules and TC in these different clinical situations.

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