分化型甲状腺癌患者超灵敏与高灵敏测定法预测受刺激甲状腺球蛋白水平的比较

Jinsun Jang, Hyun Joo Kim, Seunggyun Ha, Kyong Yeun Jung, Gyeongseo Jung, Sun Wook Cho, Do Joon Park, Gi Jeong Cheon, Young Joo Park
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引用次数: 0

摘要

背景:甲状腺球蛋白(Tg)测定是监测分化型甲状腺癌(DTC)患者的重要方面。本研究比较了超灵敏Tg (ultraTg)和高灵敏Tg (hsTg)测定在预测无促甲状腺激素刺激时受刺激Tg水平的性能。方法:共纳入268例行甲状腺全切除术、放射性碘治疗或I-123诊断扫描的DTC患者。采用hsTg (BRAHMS Dynotest Tg-plus)和ultraTg (RIAKEY Tg免疫放射测定法)测定未受刺激和受刺激的Tg水平。分析各检测方法与未受刺激Tg水平预测受刺激Tg≥1 ng/mL能力的相关性。结果:hsTg与ultraTg呈强相关(R=0.79, P0.23 ng/mL);3例在3.4 ~ 5.8年内发生结构性复发。2例患者hsTg反应良好,但ultraTg反应不确定或生化反应不完全。结论:与hsTg相比,UltraTg在预测阳性刺激Tg水平和潜在复发方面具有更高的敏感性。但其特异性较低,可能导致生化不完全反应的分类更为频繁。对于hsTg低于临界值的临床可疑病例,UltraTg可能是有益的,但其更广泛的适用性需要进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of Ultrasensitive and Highly Sensitive Assay to Predict Stimulated Thyroglobulin Levels Using Unstimulated Levels in Differentiated Thyroid Cancer Patients.

Background: Thyroglobulin (Tg) measurement is an essential aspect of monitoring for differentiated thyroid cancer (DTC) patients. This study compared the performances of ultrasensitive Tg (ultraTg) and highly sensitive Tg (hsTg) assays in predicting stimulated Tg levels without thyroid-stimulating hormone stimulation.

Methods: Overall, 268 DTC patients who had undergone total thyroidectomy and either radioiodine treatment or I-123 diagnostic scanning were included. Unstimulated and stimulated Tg levels were measured using hsTg (BRAHMS Dynotest Tg-plus) and ultraTg (RIAKEY Tg immunoradiometric assay) assays. Correlations of each assay with the ability of unstimulated Tg levels to predict stimulated Tg ≥1 ng/mL were analyzed.

Results: hsTg and ultraTg showed a strong correlation (R=0.79, P<0.01); the correlation was weaker in Tg antibody-positive patients (R=0.52). UltraTg demonstrated higher sensitivity in predicting stimulated Tg ≥1 ng/mL compared with hsTg. The optimal cut-off for ultraTg was 0.12 ng/mL (sensitivity, 72.0%; specificity, 67.2%). hsTg at 0.105 ng/mL had lower sensitivity (39.8%) but higher specificity (91.5%). Eight discordant cases with low hsTg (<0.2 ng/mL) but elevated ultraTg (>0.23 ng/mL) were identified; three developed structural recurrence within 3.4 to 5.8 years. Two patients had an excellent response according to hsTg but an indeterminate or biochemical incomplete response according to ultraTg.

Conclusion: UltraTg demonstrated higher sensitivity in predicting positive stimulated Tg levels and potential recurrence compared with hsTg. However, its lower specificity may lead to more frequent classifications of biochemical incomplete response. UltraTg may be beneficial in clinically suspicious cases where hsTg falls below the cut-off, but its broader applicability requires further investigation.

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