Molecular diagnosis of residual and recurrent thyroid cancer by amplification of thyroglobulin messenger ribonucleic acid in peripheral blood

Citation
Md. Ringel et al., Molecular diagnosis of residual and recurrent thyroid cancer by amplification of thyroglobulin messenger ribonucleic acid in peripheral blood, J CLIN END, 83(12), 1998, pp. 4435-4442
Citations number
52
Categorie Soggetti
Endocrynology, Metabolism & Nutrition","Endocrinology, Nutrition & Metabolism
Journal title
JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
ISSN journal
0021972X → ACNP
Volume
83
Issue
12
Year of publication
1998
Pages
4435 - 4442
Database
ISI
SICI code
0021-972X(199812)83:12<4435:MDORAR>2.0.ZU;2-3
Abstract
Serum thyroglobulin measurement by immunoassay is used to detect residual o r recurrent thyroid cancer after thyroid ablation. However, the usefulness of immunoassay is limited by both the requirement for thyroid hormone withd rawal to attain optimal test sensitivity and interference by antithyroglobu lin antibodies. To circumvent these problems, we amplified thyroglobulin me ssenger ribonucleic acid (mRNA) in peripheral blood using RT-PCR and compar ed the accuracy of this test to serum thyroglobulin immunoassay in patients with thyroid cancer. Thyroglobulin mRNA. was amplified from peripheral blood of 77 patients who had undergone thyroidectomy for well differentiated thyroid cancer, 68 of w hom while taking thyroid hormone for TSH suppression. Patient staging was b ased on the most recent radioiodine scan after thyroid hormone withdrawal. Ten normal control subjects were also studied. Among patients taking T-4, thyroglobulin mRNA was detected in 26 of 33 pati ents with either thyroid bed or metastatic iodine-avid tissue on most recen t withdrawal scan (79%), whereas serum thyroglobulin was detected in 12 of these 33 patients (36%; P < 0.001). Thyroglobulin mRNA was detected in 7 of 35 patients (20%) with negative radioiodine scans, 12 of 19 patients (63%) with radioiodine uptake in the thyroid bed, and all 14 patients with metas tases, including 2 patients with antithyroglobulin antibodies. Thyroglobuli n mRNA was detected in all 10 normal subjects. Epithelioid cells that stain ed strongly with antithyroglobulin antibodies were identified in blood. Detection of circulating thyroglobulin mRNA is a more sensitive marker of r esidual thyroid tissue or cancer than immunoassay for serum thyroglobulin, particularly in patients treated with thyroid hormone or who have circulati ng antithyroglobulin antibodies.