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七种血清甲状腺球蛋白检测方法在甲状腺乳头状癌和滤泡状癌患者随访中的比较

Comparison of seven serum thyroglobulin assays in the follow-up of papillary and follicular thyroid cancer patients.

作者信息

Schlumberger M, Hitzel A, Toubert M E, Corone C, Troalen F, Schlageter M H, Claustrat F, Koscielny S, Taieb D, Toubeau M, Bonichon F, Borson-Chazot F, Leenhardt L, Schvartz C, Dejax C, Brenot-Rossi I, Torlontano M, Tenenbaum F, Bardet S, Bussière F, Girard J J, Morel O, Schneegans O, Schlienger J L, Prost A, So D, Archambeaud F, Ricard M, Benhamou E

机构信息

Institut Gustave Roussy, Rue Camille Desmoulins, 94805 Villejuif Cédex, France.

出版信息

J Clin Endocrinol Metab. 2007 Jul;92(7):2487-95. doi: 10.1210/jc.2006-0723. Epub 2007 Apr 10.

Abstract

BACKGROUND

Serum thyroglobulin (Tg) is the marker of differentiated thyroid cancer after initial treatment and TSH stimulation increases its sensitivity for the diagnosis of recurrent disease.

AIM

The goal of the study is to compare the diagnostic values of seven methods for serum Tg measurement for detecting recurrent disease both during L-T4 treatment and after TSH stimulation.

METHODS

Thyroid cancer patients who had no evidence of persistent disease after initial treatment (total thyroidectomy and radioiodine ablation) were studied at 3 months on L-T4 treatment (Tg1) and then at 9-12 months after withdrawal or recombinant human TSH stimulation (Tg2). Sera with anti-Tg antibodies or with an abnormal recovery test result were excluded from Tg analysis with the corresponding assay. The results of serum Tg determination were compared to the clinical status of the patient at the end of follow-up.

RESULTS

Thirty recurrences were detected among 944 patients. A control 131I total body scan had a low sensitivity, a low specificity, and a low clinical impact. Assuming a common cutoff for all Tg assays at 0.9 ng/ml, sensitivity ranged from 19-40% and 68-76% and specificity ranged from 92-97% and 81-91% for Tg 1 and Tg2, respectively. Using assays with a functional sensitivity at 0.2-0.3 ng/ml, sensitivity was 54-63% and specificity was 89% for Tg1. Using the two methods with a lowest functional sensitivity at 0.02 and 0.11 ng/ml resulted in a higher sensitivity for Tg1 (81% and 78%), but at the expense of a loss of specificity (42% and 63%); finally, for these two methods, using an optimized functional sensitivity according to receiver operating characteristic curves at 0.22 and 0.27 ng/ml resulted in a sensitivity at 65% and specificity at 85-87% for Tg1.

CONCLUSION

Using an assay with a lower functional sensitivity may give an earlier indication of the presence of Tg in the serum on L-T4 treatment and may be used to study the trend in serum Tg without performing any TSH stimulation. Serum Tg determination obtained after TSH stimulation still permits a more reliable assessment of cure and patient's reassurance.

摘要

背景

血清甲状腺球蛋白(Tg)是分化型甲状腺癌初始治疗后的标志物,促甲状腺激素(TSH)刺激可提高其对复发疾病诊断的敏感性。

目的

本研究的目的是比较七种血清Tg检测方法在L-T4治疗期间和TSH刺激后对检测复发疾病的诊断价值。

方法

对初始治疗(甲状腺全切术和放射性碘消融)后无持续性疾病证据的甲状腺癌患者在L-T4治疗3个月时进行研究(Tg1),然后在停药或重组人TSH刺激后9-12个月时进行研究(Tg2)。含抗Tg抗体或恢复试验结果异常的血清被排除在相应检测方法的Tg分析之外。将血清Tg测定结果与随访结束时患者的临床状况进行比较。

结果

在944例患者中检测到30例复发。对照131I全身扫描的敏感性、特异性及临床影响均较低。假设所有Tg检测的共同临界值为0.9 ng/ml,Tg1和Tg2的敏感性分别为19%-40%和68%-76%,特异性分别为92%-97%和81%-91%。使用功能敏感性为0.2-0.3 ng/ml的检测方法,Tg1的敏感性为54%-63%,特异性为89%。使用功能敏感性最低的两种方法(分别为0.02和0.11 ng/ml),Tg1的敏感性更高(分别为81%和78%),但以特异性降低为代价(分别为42%和63%);最后,对于这两种方法,根据受试者操作特征曲线将功能敏感性优化至0.22和0.27 ng/ml时,Tg1的敏感性为65%,特异性为85%-87%。

结论

使用功能敏感性较低的检测方法可能会更早提示L-T4治疗期间血清中Tg的存在,可用于研究血清Tg的变化趋势而无需进行任何TSH刺激。TSH刺激后进行血清Tg测定仍能更可靠地评估治愈情况并让患者安心。

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