Exp Clin Endocrinol Diabetes 2011; 119(6): 348-352
DOI: 10.1055/s-0030-1269881
Article

© J. A. Barth Verlag in Georg Thieme Verlag KG Stuttgart · New York

Do Thyroid Cancer Patients with Basal Undetectable Tg Measured by Current Immunoassays Require rhTSH Testing?

G. Díaz-Soto1 , 2 , M. Puig-Domingo1 , I. Martínez-Pino3 , M. J. Martínez de Osaba4 , M. Mora1 , F. Rivera-Fillat4 , I. Halperin1
  • 1Servei de Endocrinologia i Nutrició, Hospital Clínic, Barcelona, Spain
  • 2Servicio de Endocrinología y Nutrición, Hospital Clínico de Valladolid, Spain. Centro de Investigación de Endocrinología y Nutrición Clínica (IEN). Facultad de Medicina de Valladolid, Spain
  • 3Centro Nacional de Epidemiología, Instituto de Salud Carlos III, Madrid, Spain. CIBER de Epidemiología y Salud Pública (CIBERESP)
  • 4Centre de Diagnostic Biomèdic, Hospital Clínic, Barcelona, Spain
Further Information

Publication History

received 13.09.2010 first decision 26.10.2010

accepted 23.11.2010

Publication Date:
24 January 2011 (online)

Abstract

Objective: To evaluate the predictive value of disease free status of basal thyroglobulin (Tg) in differentiated thyroid carcinoma (DTC).

Design: Basal and recombinant human TSH (rhTSH) stimulated Tg measured with a commercial immunoassay (Liaison DiaSorin, Italial), neck ultrasonography (US) and fine needle aspiration cytology if required were performed in DTC patients followed prospectively for 6.8 years in a university hospital. 92 consecutive DTC patients were included. 74 patients with basal and stimulated Tg <1.0 ng/ml and Tg antibodies and US negative were considered as disease-free and persistent/recurrent disease was detected in 18 patients. In 25/74 disease-free patients rhTSH test was repeated within one year.

Results: 63/92 patients had undetectable basal Tg (<0.5 ng/ml), with rhTSH-Tg <0.5 ng/ml in 52, in 6 rhTSH-Tg between 0.5 and 1 ng/ml, in 2 between 1–2 ng/ml (disease-free after 3 years of follow-up) and >2.0 ng/ml (mean 4.1±2.4 ng/ml) in another 3, with US lymphatic metastasis confirmed histologically. Disease-free state was predicted with a sensitivity (S) of 66.7% and specificity (Sp) of 75.7% for basal Tg-0.5 ng/ml, and S 100% and Sp 85.1% for stimulated Tg-0.92. rhTSH test and US were repeated within one year in 25 disease-free patients with Tg<1.0 ng/ml. No further elevation below 1 ng/ml was observed.

Conclusions: Low risk patients with undetectable basal Tg measured with current commercially available immunoassays should be followed with at least one rhTSH stimulated Tg and neck US because of the insufficient predictive value for recurrence/persistent disease of basal Tg.

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Correspondence

Dr. G. Díaz-Soto

Hospital Clinico de Valladolid

Servicio de Endocrinología

C/Ramon y Cajal n 3. 47004

Valladolid

Spain

Phone: +34/983/24 00 00 ext: 21 615

Fax: +34/934/51 66 38

Email: diazsotogonzalo@gmail.com

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