Zhang Lin, Smola Brian, Lew Madelyn, Pang Judy, Cantley Richard, Pantanowitz Liron, Heider Amer, Jing Xin
Department of Pathology and Clinical Laboratories, University of Michigan, Ann Arbor, Michigan, USA.
Diagn Cytopathol. 2021 Aug;49(8):921-927. doi: 10.1002/dc.24765. Epub 2021 May 22.
Afirma gene expression classifier (GEC) is an adjunct to thyroid fine needle aspiration shown to improve pre-operative risk assessment and reduce unnecessary surgery of indeterminate thyroid nodules. Genomic sequencing classifier (GSC) is a newer version aiming to improve specificity and positive predictive value (PPV) of Afirma testing. There are limited studies comparing GSC vs GEC. This study was undertaken to compare these classifiers in terms of diagnostic performance and effect on clinical management of indeterminate thyroid nodules.
The study cohort consisted of patients with thyroid nodules that had a recurrent cytologic diagnosis of atypia of undetermined significance/follicular lesion of undetermined significance (AUS/FLUS) and were tested by either GEC or GSC. Patient demographics, nodule size, and clinical follow-up were recorded. Benign call rate (BCR) of Afirma testing, rate of subsequent surgery (RSS), rate of histology-confirmed malignancy (RHM), as well as diagnostic sensitivity, specificity, PPV, negative predicative value (NPV), and accuracy were calculated and compared between GSC and GEC cohorts.
Among 264 AUS/FLUS thyroid nodules, 127 and 137 were tested with GEC and GSC, respectively. Compared to GEC, GSC demonstrated increased BCR (77.3% vs 52%), decreased RSS (31.4% vs 51.2%), greater RHM (29% vs 9.8%) associated with a suspicious Afirma result, as well as improved specificity (82.8% vs 54.5%), PPV (29% vs 9.8%), and diagnostic accuracy (83.9% vs 56.7%), while maintaining high sensitivity and NPV.
Afirma GSC substantially improved BCR, RSS, RHM, and diagnostic performance, enhancing appropriate triage and thereby helped avoid unnecessary surgery in AUS/FLUS thyroid nodules.
Afirma基因表达分类器(GEC)是甲状腺细针穿刺活检的辅助手段,已证实可改善术前风险评估并减少不确定甲状腺结节的不必要手术。基因组测序分类器(GSC)是一个较新的版本,旨在提高Afirma检测的特异性和阳性预测值(PPV)。比较GSC与GEC的研究有限。本研究旨在比较这两种分类器在诊断性能以及对不确定甲状腺结节临床管理的影响方面的差异。
研究队列包括甲状腺结节患者,这些患者的细胞学诊断反复为意义不明确的非典型性/意义不明确的滤泡性病变(AUS/FLUS),并接受了GEC或GSC检测。记录患者的人口统计学信息、结节大小和临床随访情况。计算并比较GSC和GEC队列中Afirma检测的良性检出率(BCR)、后续手术率(RSS)、组织学确诊恶性肿瘤率(RHM),以及诊断敏感性、特异性、PPV、阴性预测值(NPV)和准确性。
在264个AUS/FLUS甲状腺结节中,分别有127个和137个接受了GEC和GSC检测。与GEC相比,GSC显示出更高的BCR(77.3%对52%)、更低的RSS(31.4%对51.2%)、与可疑Afirma结果相关的更高RHM(29%对9.8%),以及更高的特异性(82.8%对54.5%)、PPV(29%对9.8%)和诊断准确性(83.9%对56.7%),同时保持高敏感性和NPV。
Afirma GSC显著改善了BCR、RSS、RHM和诊断性能,加强了合理的分类,从而有助于避免AUS/FLUS甲状腺结节的不必要手术。