Horm Metab Res 2018; 50(08): 602-608
DOI: 10.1055/a-0651-4913
Endocrine Care
© Georg Thieme Verlag KG Stuttgart · New York

Increased Numbers of Circulating Tumor Cells in Thyroid Cancer Patients

Margret Ehlers*
1   Division for Specific Endocrinology, Medical Faculty, University of Duesseldorf, Duesseldorf, Germany
,
Stephanie Allelein*
1   Division for Specific Endocrinology, Medical Faculty, University of Duesseldorf, Duesseldorf, Germany
,
Franziska Schwarz
1   Division for Specific Endocrinology, Medical Faculty, University of Duesseldorf, Duesseldorf, Germany
,
Hubertus Hautzel
2   Clinic for Nuclear Medicine, University Hospital Duesseldorf, Duesseldorf, Germany
,
Anne Kuebart
1   Division for Specific Endocrinology, Medical Faculty, University of Duesseldorf, Duesseldorf, Germany
,
Mathias Schmidt
1   Division for Specific Endocrinology, Medical Faculty, University of Duesseldorf, Duesseldorf, Germany
,
Matthias Haase
1   Division for Specific Endocrinology, Medical Faculty, University of Duesseldorf, Duesseldorf, Germany
,
Till Dringenberg
1   Division for Specific Endocrinology, Medical Faculty, University of Duesseldorf, Duesseldorf, Germany
,
Matthias Schott
1   Division for Specific Endocrinology, Medical Faculty, University of Duesseldorf, Duesseldorf, Germany
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Weitere Informationen

Publikationsverlauf

received 17. Mai 2018

accepted 25. Juni 2018

Publikationsdatum:
06. August 2018 (online)

Abstract

Circulating tumor cells (CTCs) have been shown to be a valuable prognostic marker for different solid cancers. Within the present study we quantified CTCs in thyroid cancer (TC) patients. Special focus was given to disease-free PTC patients with undetectable serum thyroglobulin (Tg) levels. Altogether, 67 TC patients (33 papillary, 20 follicular, 14 medullary) were included in the study. CTC numbers, which were normalized to 3.3×105 peripheral blood mononuclear cells, were correlated with clinical outcome. TC patients had significantly higher CTC numbers compared to controls. The number of CTCs correlated to the initial tumor stage. Importantly, in comparison to controls, differentiated TC patients with serum Tg levels<0.3 ng/ml (no evidence of tumor recurrence) revealed a significantly higher amount of CTCs, also associated to their former tumor stage. Regarding the tumor-free papillary TC (PTC) patients the number of CTCs additionally correlated to the time point of radioiodine (RI) therapy: PTC patients with RI therapies>8 years before CTC measurement had significantly higher CTC numbers compared to those with RI therapy<8 years ago. We found a clear correlation between the number of CTCs and the tumor stage. Importantly, PTC patients who are in remission may still have increased numbers of CTCs. Follow-up analyses in these patients will reveal whether these data will have a clinical impact.

* Both authors contributed equally to this work


 
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