1 Department of Endocrinology and University of Groningen, Groningen, The Netherlands.
2 Department of Nuclear Medicine and Molecular Imaging; University of Groningen, Groningen, The Netherlands.
Thyroid. 2019 Jan;29(1):71-78. doi: 10.1089/thy.2018.0195. Epub 2018 Dec 18.
Thyroglobulin (Tg) is an established tumor marker in differentiated thyroid carcinoma (DTC). However, Tg assays can be subject to interference by autoantibodies against Tg (TgAbs). No clinical consensus exists on the cutoff value of TgAb positivity and its relationship to Tg assay interference. The aims of this study were to investigate the most applicable cutoff value for TgAb positivity in clinical practice and to evaluate whether tumor characteristics differ between TgAb+ and TgAb- patients during ablation therapy using the manufacturer's cutoff (MCO) and institutional cutoff (ICO).
This single-center cohort study included 230 DTC patients diagnosed between January 2006 and December 2014. Serum Tg and TgAbs were measured with the Tg-IRMA (Thermo Fisher Scientific) and ARCHITECT Anti-Tg (Abbott Laboratories) assays. Patients were divided into TgAb- and TgAb+ based on the limit of detection (LoD; ≥0.07 IU/mL), functional sensitivity (FS; ≥0.31 IU/mL), MCO (≥4.11 IU/mL), and ICO (≥10 IU/mL).
All patients were TgAb+ based on the LoD; one patient was negative on FS. Fifty-five (23.9%) and 34 (14.8%) patients had TgAbs above the MCO and ICO, respectively. Histology, presence of multifocality, tumor-node-metastasis, and American Thyroid Assocation risk stratification did not differ between TgAb- and TgAb+ patients using MCO and ICO during ablation.
This study supports the use of a higher cutoff value than that of the FS for TgAb positivity in clinical settings. The LoD and FS are too sensitive to discriminate TgAb positivity and negativity in DTC patients during ablation therapy. The presence of TgAbs during ablation is not related to tumor characteristics and risk profile. This implies that TgAb positivity should not be considered a separate risk factor.
甲状腺球蛋白(Tg)是分化型甲状腺癌(DTC)的一种既定肿瘤标志物。然而,Tg 检测可能会受到针对 Tg 的自身抗体(TgAbs)的干扰。目前尚未就 TgAb 阳性的截止值及其与 Tg 检测干扰的关系达成临床共识。本研究旨在探讨在临床实践中 TgAb 阳性最适用的截止值,并评估在消融治疗中使用制造商的截止值(MCO)和机构的截止值(ICO)时,TgAb+和 TgAb-患者之间的肿瘤特征是否存在差异。
这项单中心队列研究纳入了 2006 年 1 月至 2014 年 12 月期间诊断的 230 例 DTC 患者。使用 Tg-IRMA(赛默飞世尔科技)和 ARCHITECT Anti-Tg(雅培实验室)检测试剂盒测量血清 Tg 和 TgAbs。根据检测限(LoD;≥0.07 IU/mL)、功能灵敏度(FS;≥0.31 IU/mL)、MCO(≥4.11 IU/mL)和 ICO(≥10 IU/mL),将患者分为 TgAb-和 TgAb+。
所有患者根据 LoD 均为 TgAb+;有一位患者 FS 检测为阴性。55 例(23.9%)和 34 例(14.8%)患者的 TgAbs 高于 MCO 和 ICO。使用 MCO 和 ICO 时,TgAb-和 TgAb+患者的组织学、多灶性存在、肿瘤-淋巴结-转移和美国甲状腺协会风险分层并无差异。
本研究支持在临床环境中使用高于 FS 的截止值来判断 TgAb 阳性。在 DTC 患者消融期间,LoD 和 FS 过于敏感,无法区分 TgAb 阳性和阴性。消融期间存在 TgAbs 与肿瘤特征和风险概况无关。这意味着 TgAb 阳性不应被视为单独的危险因素。