Department of Pathology, Duke University Medical Center, Durham, North Carolina.
Cancer Cytopathol. 2018 Jul;126(7):471-480. doi: 10.1002/cncy.21993. Epub 2018 Apr 10.
The ThyroSeq mutational panel and Afirma gene expression classifier (GEC) are used to risk stratify cytologically indeterminate thyroid nodules. In the current study, the authors evaluated the performance of these tests within the context of ultrasonographic features and with the incorporation of the noninvasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTP) nomenclature.
The authors reviewed nodules using ThyroSeq or Afirma GEC testing. For nodules that were surgically resected, both tests were studied within the context of ultrasound findings, comparing performance stratified by the 2015 American Thyroid Association guideline (ATA 2015) sonographic patterns and assessing the positive predictive value (PPV) of these tests both including and excluding NIFTP in the malignant category.
A total of 304 cases were identified, 119 of which were resected. All cases that met the criteria for NIFTP on excision demonstrated either high-risk mutations on ThyroSeq or a "suspicious" result on Afirma GEC. When NIFTP cases were shifted from the malignant to nonmalignant category, the PPV of "positive" tests for both ThyroSeq and Afirma GEC decreased from 42.9% to 14.3% (an absolute decrease of 28.6%) and 30.1% to 25.3% (an absolute decrease of 4.8%), respectively. No cases of malignancy were found in the ATA 2015 "very low suspicion" group, even with a "suspicious" Afirma GEC result.
Both the ThyroSeq and Afirma GEC tests demonstrated decreases in the PPV when NIFTP was considered nonmalignant. In the era of NIFTP, a "positive" test result for either the Afirma GEC or ThyroSeq should be interpreted in light of clinical factors and should not exclude conservative (ie, lobectomy) surgical management. ATA 2015 "very low suspicion" nodules, even with "suspicious" Afirma GEC results, were not found to demonstrate malignancy in this series. Cancer Cytopathol 2018. © 2018 American Cancer Society.
ThyroSeq 突变面板和 Afirma 基因表达分类器(GEC)用于对细胞学不确定的甲状腺结节进行风险分层。在本研究中,作者评估了这些检测在超声特征背景下的表现,并纳入了非侵袭性滤泡性甲状腺肿瘤伴乳头状核特征(NIFTP)命名法。
作者使用 ThyroSeq 或 Afirma GEC 检测对结节进行了回顾。对于接受手术切除的结节,根据 2015 年美国甲状腺协会指南(ATA 2015)的超声模式对这两种检测进行了分层,并评估了这些检测在纳入和排除恶性分类中的 NIFTP 时的阳性预测值(PPV)。
共确定了 304 例病例,其中 119 例接受了切除。所有符合 NIFTP 标准的切除病例均在 ThyroSeq 上显示高风险突变,或在 Afirma GEC 上显示“可疑”结果。当将 NIFTP 病例从恶性转移到非恶性类别时,ThyroSeq 和 Afirma GEC 的“阳性”检测的 PPV 分别从 42.9%降至 14.3%(绝对下降 28.6%)和从 30.1%降至 25.3%(绝对下降 4.8%)。在 ATA 2015 年的“非常低可疑”组中未发现恶性肿瘤病例,即使 Afirma GEC 结果可疑。
当 NIFTP 被认为是非恶性时,ThyroSeq 和 Afirma GEC 检测的 PPV 均降低。在 NIFTP 时代,Afirma GEC 或 ThyroSeq 的“阳性”检测结果应根据临床因素进行解释,不应排除保守(即,叶切除术)手术管理。在本系列中,即使 Afirma GEC 结果可疑,ATA 2015 年的“非常低可疑”结节也未发现恶性肿瘤。癌症细胞病理学 2018. © 2018 美国癌症协会。