Section of Endocrine Surgery, UCLA David Geffen School of Medicine, Los Angeles, CA, USA.
Division of Endocrinology, Diabetes, and Metabolism, UCLA David Geffen School of Medicine, Los Angeles, CA, USA.
J Clin Endocrinol Metab. 2021 Mar 8;106(3):e1240-e1247. doi: 10.1210/clinem/dgaa887.
Molecular testing to refine the diagnosis of cytologically indeterminate thyroid nodules has become increasingly popular, but data on long-term durability of test results and the rate of delayed operation are limited.
Determine the delayed rate of surgical resection in indeterminate nodules with benign/negative molecular testing and the risk of false-negative molecular test results.
Prospective follow-up of the Gene Expression Classifier vs Targeted Next-Generation Sequencing in the Management of Indeterminate Thyroid Nodules randomized controlled trial comparing the diagnostic test performance of Afirma Gene Expression Classifier and ThyroSeq v2.
University of California, Los Angeles.
Patients who underwent thyroid biopsy with indeterminate (Bethesda III/IV) cytology (April 2016 to July 2017).
Ultrasound surveillance.
False-negative rate of molecular testing.
Of 95 indeterminate nodules with negative/benign molecular test results, 12 nodules underwent immediate resection (11 benign nodules, 1 noninvasive follicular thyroid neoplasm nodule with papillary-like nuclear features). Nonoperative management was pursued for 83 (87.4%) nodules. The median surveillance was 26.7 months. Ten nodules were resected during surveillance and malignancy was identified in 4 nodules (overall false-negative rate of 5.8%). In the 4 malignant nodules that underwent delayed operation, surgery was prompted by sonographic changes during surveillance.
The majority of indeterminate nodules with negative molecular testing have a stable clinical course over 3 years of follow-up, but our finding of a 6% false-negative rate highlights the importance of continuing sonographic surveillance. Long-term studies are needed to determine the optimal length of follow-up.
为了更精确地诊断细胞学不确定的甲状腺结节,对其进行分子检测的做法越来越普及,但有关长期检测结果稳定性和延迟手术率的数据却有限。
明确良性/阴性分子检测结果的不确定甲状腺结节延迟手术率和假阴性分子检测结果的风险。
对比 Afirma 基因表达分类器和 ThyroSeq v2 的诊断测试性能,对“基因表达分类器与靶向下一代测序在不确定甲状腺结节管理中的应用”(Gene Expression Classifier vs Targeted Next-Generation Sequencing in the Management of Indeterminate Thyroid Nodules,GEMINI)随机对照试验进行前瞻性随访。
加利福尼亚大学洛杉矶分校。
行甲状腺活检的不确定(Bethesda III/IV)细胞学患者(2016 年 4 月至 2017 年 7 月)。
超声监测。
分子检测的假阴性率。
95 个阴性/良性分子检测结果的不确定结节中,有 12 个结节立即行切除术(11 个良性结节,1 个具乳头状核特征的非侵袭性滤泡甲状腺肿瘤结节)。83 个(87.4%)未行手术,中位随访时间为 26.7 个月。10 个结节在随访期间接受了手术,其中 4 个结节发现恶性肿瘤(总的假阴性率为 5.8%)。在 4 个延迟手术的恶性结节中,手术是基于随访期间的超声变化而进行的。
大多数阴性分子检测结果的不确定结节在 3 年的随访中具有稳定的临床过程,但我们发现有 6%的假阴性率,这突出了继续进行超声监测的重要性。需要进行长期研究以确定最佳的随访时间。