Gene Expression Classifier vs Targeted Next-Generation Sequencing in the Management of Indeterminate Thyroid Nodules

被引:42
作者
Livhits, Masha J. [1 ]
Kuo, Eric J. [1 ]
Leung, Angela M. [2 ,3 ]
Rao, Jianyu [4 ]
Levin, Mary [4 ]
Douek, Michael L. [5 ]
Beckett, Katrina R. [5 ]
Zanocco, Kyle A. [1 ]
Cheung, Dianne S. [2 ]
Gofnung, Yaroslav A. [2 ]
Smooke-Praw, Stephanie [2 ]
Yeh, Michael W. [1 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Sect Endocrine Surg, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Div Endocrinol Diabet & Metab, Los Angeles, CA 90095 USA
[3] VA Greater Los Angeles Healthcare Syst, Div Endocrinol Diabet & Metab, Los Angeles, CA 90073 USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, David Geffen Sch Med, Dept Radiol, Los Angeles, CA 90095 USA
关键词
ENCAPSULATED FOLLICULAR VARIANT; ASSOCIATION GUIDELINES; UNITED-STATES; TASK-FORCE; CANCER; PERFORMANCE; DIAGNOSIS; CARCINOMA; AFIRMA; NEOPLASM;
D O I
10.1210/jc.2017-02754
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Molecular testing has reduced the need for diagnostic hemithyroidectomy for indeterminate thyroid nodules. No studies have directly compared molecular testing techniques. Objective: Compare the diagnostic performance of Afirma Gene Expression Classifier (GEC) with that of ThyroSeq v2 next-generation sequencing assay. Design: Parallel randomized trial, monthly block randomization of patients with Bethesda III/IV cytology to GEC or ThyroSeq v2. Setting: University of California, Los Angeles. Participants: Patients who underwent thyroid biopsy (April 2016 to June 2017). Intervention: Testing with GEC or ThyroSeq v2. Main Outcome Measure: Molecular test performance. Results: Of 1372 thyroid nodules, 176 (13%) had indeterminate cytology and 149 of 157 eligible indeterminate nodules (95%) were included in the study. Of nodules tested with GEC, 49% were suspicious, 43% were benign, and 9% were insufficient. Of nodules tested with ThyroSeq v2, 19% were mutation positive, 77% were mutation negative, and 4% were insufficient. The specificities of GEC and ThyroSeq v2 were 66% and 91%, respectively (P = 0.002); the positive predictive values of GEC and ThyroSeq v2 were 39% and 57%, respectively. Diagnostic hemithyroidectomy was avoided in 28 patients tested with GEC (39%) and 49 patients tested with ThyroSeq v2 (62%). Surveillance ultrasonography was available for 46 nodules (45 remained stable). Conclusions: ThyroSeq v2 had higher specificity than Afirma GEC and allowed more patients to avoid surgery. Long-term surveillance is necessary to assess the false-negative rate of these particular molecular tests. Further studies are required for comparison with other available molecular diagnostics and for newer tests as they are developed.
引用
收藏
页码:2261 / 2268
页数:8
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