Valderrabano Pablo, Khazai Laila, Leon Marino E, Thompson Zachary J, Ma Zhenjun, Chung Christine H, Hallanger-Johnson Julie E, Otto Kristen J, Rogers Kara D, Centeno Barbara A, McIver Bryan
Department of Head and Neck-Endocrine OncologyH. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA
Department of Anatomic PathologyH. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Endocr Relat Cancer. 2017 Mar;24(3):127-136. doi: 10.1530/ERC-16-0512. Epub 2017 Jan 19.
ThyroSeq v2 claims high positive (PPV) and negative (NPV) predictive values in a wide range of pretest risks of malignancy in indeterminate thyroid nodules (ITNs) (categories B-III and B-IV of the Bethesda system). We evaluated ThyroSeq v2 performance in a cohort of patients with ITNs seen at our Academic Cancer Center from September 2014 to April 2016, in light of the new diagnostic criteria for non-invasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTP). Our study included 182 patients (76% female) with 190 ITNs consecutively tested with ThyroSeq v2. Patient treatment followed our institutional thyroid nodule clinical pathway. Histologies of nodules with follicular variant papillary thyroid carcinoma or NIFTP diagnoses were reviewed, with reviewers blinded to molecular results. ThyroSeq v2 performance was calculated in nodules with histological confirmation. We identified a mutation in 24% (45) of the nodules. Mutations in were the most prevalent (21), but the positive predictive value of this mutation was much lower (31%) than that in prior reports. In 102 resected ITNs, ThyroSeq v2 performance was as follows: sensitivity 70% (46-88), specificity 77% (66-85), PPV 42% (25-61) and NPV 91% (82-97). The performance in B-IV nodules was significantly better than that in B-III nodules (area under the curve 0.84 vs 0.57, respectively; = 0.03), where it was uninformative. Further studies evaluating ThyroSeq v2 performance are needed, particularly in B-III.
ThyroSeq v2在不确定甲状腺结节(ITN)(贝塞斯达系统的B-III和B-IV类)的广泛恶性肿瘤预测试风险中具有较高的阳性(PPV)和阴性(NPV)预测值。鉴于具有乳头样核特征的非侵袭性滤泡性甲状腺肿瘤(NIFTP)的新诊断标准,我们评估了2014年9月至2016年4月在我们学术癌症中心就诊的ITN患者队列中ThyroSeq v2的性能。我们的研究纳入了182例患者(76%为女性),他们连续接受了ThyroSeq v2检测,共检测了190个ITN。患者的治疗遵循我们机构的甲状腺结节临床路径。对具有滤泡变异型乳头状甲状腺癌或NIFTP诊断的结节组织学进行了回顾,审阅者对分子结果不知情。在组织学确诊的结节中计算ThyroSeq v2的性能。我们在24%(45个)的结节中发现了突变。 中的突变最为普遍(21个),但该突变的阳性预测值远低于先前报告(31%)。在102个切除的ITN中,ThyroSeq v2的性能如下:敏感性70%(46-88),特异性77%(66-85),PPV 42%(25-61),NPV 91%(82-97)。B-IV类结节中的性能明显优于B-III类结节(曲线下面积分别为0.84和0.57; = 0.03),在B-III类结节中该检测无信息价值。需要进一步研究评估ThyroSeq v2的性能,特别是在B-III类结节中。