Cicogna Julia Isabel Richter, Noguchi Sophia Yada, Cury Adriano Namo, Negra Giovanna Marcela Vieira Della, Fraga Laís de Oliveira Teles, Schalch Marcelo Soares, de Cicco Rafael, Silva Carolina Ferraz da, Padovani Rosália Do Prado
Faculdade de Ciências Médicas da Santa Casa de São Paulo (Faculty of Medical Sciences of Santa Casa de São Paulo), São Paulo, Brazil.
Irmandade da Santa Casa de Misericórdia de São Paulo, São Paulo, Brazil.
Clin Endocrinol (Oxf). 2025 Aug;103(2):260-268. doi: 10.1111/cen.15260. Epub 2025 May 4.
High-risk differentiated thyroid cancer (DTC) patients show variable outcomes. While postoperative stimulated thyroglobulin (STg) is a recognized predictive marker, the prognostic significance of unstimulated thyroglobulin (UTg) is still unexplored. This study aims to assess the prognostic value of postoperative UTg in high-risk DTC patients.
Retrospective cohort study (2015-2024) at two Brazilian tertiary hospitals.
One thousand DTC patients were identified, of which 144 were high-risk. Fifty seven patients met the inclusion criteria.
Clinical, pathological, and laboratory data were collected. Outcomes were categorized as favorable (excellent/indeterminate responses) or unfavorable (biochemical/structural incomplete responses). Receiver Operating Characteristic (ROC) curves determined cutoff values for predicting outcomes and metastases.
Significant predictors of unfavorable outcomes included advanced age (p = 0.048), larger tumor size (p = 0.002), higher UTg (p < 0.001), and STg (p < 0.001). UTg was an independent risk factor for 1-year outcomes (OR = 0.008; 95% CI: 0.001-0.088; p < 0.001). UTg cutoff of 2.1 ng/mL distinguished outcomes with high sensitivity (83.3%), specificity (96.0%), and accuracy (90.7%). A higher cutoff of 3.8 ng/mL identified metastases (sensitivity 86.4%, specificity 90.5%). UTg showed non-inferiority to stimulated thyroglobulin (STg) in predicting outcomes (p = 0.964) and metastasis (p = 0.980).
Postoperative UTg is a strong prognostic marker in high-risk DTC patients, providing a non-inferior alternative to STg with greater accessibility and fewer side effects. We propose a clinical algorithm to optimize the management of these cases. When UTg levels exceed 2.1 ng/mL, particularly higher than 3.8 ng/mL, investigation of potentially resectable metastatic foci should be considered before radioiodine therapy. Prospective studies are needed to validate this algorithm.
高危分化型甲状腺癌(DTC)患者的预后各不相同。虽然术后刺激甲状腺球蛋白(STg)是一种公认的预测标志物,但未刺激甲状腺球蛋白(UTg)的预后意义仍未得到探索。本研究旨在评估术后UTg在高危DTC患者中的预后价值。
对巴西两家三级医院进行的回顾性队列研究(2015 - 2024年)。
共识别出1000例DTC患者,其中144例为高危患者。57例患者符合纳入标准。
收集临床、病理和实验室数据。结局分为良好(优秀/不确定反应)或不良(生化/结构不完全反应)。采用受试者操作特征(ROC)曲线确定预测结局和转移的临界值。
不良结局的显著预测因素包括高龄(p = 0.048)、肿瘤较大(p = 0.002)、UTg较高(p < 0.001)和STg较高(p < 0.001)。UTg是1年结局的独立危险因素(OR = 0.008;95% CI:0.001 - 0.088;p < 0.001)。UTg临界值为2.1 ng/mL时,区分结局的灵敏度高(83.3%)、特异性高(96.0%)、准确性高(90.7%)。临界值为3.8 ng/mL时可识别转移(灵敏度86.4%,特异性90.5%)。在预测结局(p = 0.964)和转移(p = 0.980)方面,UTg显示出不劣于刺激甲状腺球蛋白(STg)。
术后UTg是高危DTC患者的一个强有力的预后标志物,是STg的非劣效替代指标,具有更高的可及性和更少的副作用。我们提出了一种临床算法以优化这些病例的管理。当UTg水平超过2.1 ng/mL,特别是高于3.8 ng/mL时,在放射性碘治疗前应考虑对潜在可切除的转移灶进行检查。需要进行前瞻性研究来验证该算法。