Nuklearmedizin 2012; 51(06): 217-222
DOI: 10.3413/Nukmed-0501-12-05
Original article
Schattauer GmbH

Estimation of tumour mass in patients with differentiated thyroid carcinoma using serum thyroglobulin

Abschätzung der Tumormasse bei Patienten mit differenziertem Schilddrüsenkarzinom anhand des Tumormarkers Serum-Thyreoglobulin
S. J. Rosenbaum-Krumme
1   Department of Nuclear Medicine, University Hospital Essen, Germany
,
M. Wieduwilt
1   Department of Nuclear Medicine, University Hospital Essen, Germany
,
J. Nagarajah
1   Department of Nuclear Medicine, University Hospital Essen, Germany
,
A. Bockisch
1   Department of Nuclear Medicine, University Hospital Essen, Germany
,
W. Jentzen
1   Department of Nuclear Medicine, University Hospital Essen, Germany
› Author Affiliations
Further Information

Publication History

received: 02 May 2012

accepted in revised form: 23 June 2012

Publication Date:
29 December 2017 (online)

Summary

Serum thyroglobulin (Tg) is a reliable tumour marker in follow-up of patients with differentiated thyroid carcinoma (DTC). A positive correlation between Tg level and tumour mass was recently observed, but no attempts were made to derive a numerical relation. The aim of this study was to derive a numerical relationship between serum Tg level and tumour mass that allows optimizing the diagnostic procedures. Patients, method: 78 DTC patients with tumour lesions in either 124I-NaI or 18F-FDG PET/CT were included. For each patient, the total tumour mass was determined functionally in iodine- and FDG-positive lesions as well as morphologically in only CTpositive lesions. The serum Tg level was measured under TSH stimulation prior to imaging. Regression analyses were performed to derive an approach for estimation of the total tumour mass based on Tg levels. Results: A positive correlation of serum Tg and tumour mass was confirmed and a mathematical expression was given to estimate the tumour mass along with its 95% confidence interval using only the serum Tg level. The results demonstrated that the range of predicted tumour mass was higher per serum Tg unit for iodinepositive lesions than for FDG-positive tumour lesions and was higher for follicular than for papillary thyroid carcinoma. Conclusion: This study provides an approach to estimate the tumour mass and its 95% confidence intervals in DTC patients using the serum Tg level. The range of the estimated tumour mass for a given Tg level is rather large, and therefore, the approach is of limited value in clinical application.

Zusammenfassung

Serum-Thyreoglobulin (Tg) ist ein verlässlicher Tumormarker in der Nachsorge des differenzierten Schilddrüsenkarzinoms (DTC). Eine positive Korrelation zwischen Tg-Konzentration und Tumormasse ist bekannt, jedoch wurde bislang keine numerische Beziehung hergestellt. Ziel dieser Studie war es, diese numerische Beziehung zwischen Serum-Tg-Konzentration und Tumormasse herzustellen, um den Einsatz von diagnostischen Modalitäten zu optimieren. Patienten, Methode: DTC-Patienten (n = 78) mit im 124I-NaI- oder 18F-FDGPET/ CT nachweisbaren Tumorläsionen wurden eingeschlossen. Für jeden Patienten wurde die komplette Tumormasse entweder funktionell aus Iod- oder FDG-positiven Tumorläsionen oder morphologisch bei nur CT-positiven Läsionen bestimmt. Die Serum-Tg-Konzentration wurde unmittelbar vor der Bildgebung unter TSH-Stimulation bestimmt. Zur Abschätzung der gesamten Tumormasse anhand der Tg-Konzentration wurden Regressionsanalysen durchgeführt. Ergebnis: Eine positive Korrelation zwischen Tg und Tumormasse konnte bestätigt werden und eine numerische Beziehung zur Abschätzung der Tumormasse sowie des 95%-Konfidenzintervalls auf der Basis des Serum-Tg-Spiegels konnte erstellt werden. Die Spannweite der errechneten Tumormasse pro Tg-Einheit war größer für rein Iod-positive Tumorläsionen im Vergleich zu rein FDG-positiven, ebenso war diese größer für follikuläre- im Vergleich zu papillären DTC. Schlussfolgerung: Diese Studie bietet eine Möglichkeit zur Abschätzung der Tumormasse und des 95%-Konfidenzintervalls anhand des Serum-Tg-Spielgels für DTC-Patienten. Die Spannbreite der abgeschätzten Tumormasse bei einem bestimmten Tg ist jedoch sehr groß, weshalb dieser Ansatz in der klinischen Routine von limitiertem Wert ist.

 
  • References

  • 1 Bachelot A, Cailleux AF, Klain M. et al. Relationship between tumor burden and serum thyroglobulin level in patients with papillary and follicular thyroid carcinoma. Thyroid 2002; 12: 707-711.
  • 2 Cooper DS, Doherty GM, Haugen BR. et al. Revised American Thyroid Association management guidelines for patients with thyroid nodules and differentiated thyroid cancer. Thyroid 2009; 19: 1167-1214.
  • 3 Dietlein A, Scheidhauer K, Voth E. et al. Fluorine-18 fluorodeoxyglucose positron emission tomography and iodine-131 whole-body scintigraphy in the follow-up of differentiated thyroid cancer. Eur J Nucl Med 1997; 24: 1342-1348.
  • 4 Dralle H, Schwarzrock R, Lang W. et al. Comparison of histology and immunohistochemistry with thyroglobulin serum levels and radioiodine uptake in recurrences and metastases of differentiated thyroid carcinomas. Acta Endocrinol (Copenh) 1985; 108: 504-510.
  • 5 Eustatia-Rutten CF, Smit JW, Romijn JA. et al. Diagnostic value of serum thyroglobulin measurements in the follow-up of differentiated thyroid carcinoma, a structured meta-analysis. Clin Endocrinol (Oxf) 2004; 61: 61-74.
  • 6 Giovanella L, Ceriani L, De Palma D. et al. Relationship between serum thyroglobulin and 18FDG-PET/CT in 131I-negative differentiated thyroid carcinomas. Head Neck 2012; 34: 626-631.
  • 7 Giovanella L, Suriano S, Ceriani L. et al. Papillary carcinoma simultaneously involving thyroid, neck lymph-nodes, ovary and bone marrow. Nuklearmedizin 2010; 49: N66-N68.
  • 8 Görges R, Bockisch A. Thyroglobulin as Specific Tumor Marker in Differentiated Thyroid Cancer. Biersack HJ, Grünwald F. Thyroid Cancer.. Berlin, Heidelberg: Springer; 2005: 221-232.
  • 9 Jentzen W, Freudenberg L, Eising EG. et al. Optimized 124I PET dosimetry protocol for radioiodine therapy of differentiated thyroid cancer. J Nucl Med 2008; 49: 1017-1023.
  • 10 Jentzen W, Freudenberg L, Eising EG. et al. Segmentation of PET volumes by iterative image thresholding. J Nucl Med 2007; 48: 108-114.
  • 11 Jentzen W, Weise R, Kupferschläger J. et al. Iodine-124 PET dosimetry in differentiated thyroid cancer: recovery coefficient in 2D and 3D modes for PET(/CT) systems. Eur J Nucl Med Mol Imaging 2008; 35: 611-623.
  • 12 Kloos RT. Approach to the patient with a positive serum thyroglobulin and a negative radioiodine scan after initial therapy for differentiated thyroid cancer. J Clin Endocrinol Metab 2008; 93: 1519-1525.
  • 13 Marcocci C, Pacini F, Elisei R. et al. Clinical and biologic behavior of bone metastases from differentiated thyroid carcinoma. Surgery 1989; 106: 960-966.
  • 14 Müller-Gärtner HW, Schneider C. Clinical evaluation of tumor characteristics predisposing serum thyroglobulin to be undetectable in patients with differentiated thyroid cancer. Cancer 1988; 61: 976-998.
  • 15 Pacini F, Schlumberger M, Dralle H. et al. European consensus for the management of patients with differentiated thyroid carcinoma of the follicular epithelium. Eur J Endocrinol 2006; 154: 787-780.
  • 16 Pittas AG, Adler M, Fazzari M. et al. Bone metastases from thyroid carcinoma: clinical characteristics and prognostic variables in one hundred forty six patients. Thyroid 2000; 10: 261-268.
  • 17 Proye CA, Dromer DH, Camaille BM. et al. Is it still worthwhile to treat bone metastases from differentiated thyroid carcinoma with radioactive iodine?. World J Surg 1992; 16: 640-646.
  • 18 Schönberger J, Rüschoff J, Grimm D. et al. Glucose transporter 1 gene expression is related to thyroid neoplasms with an unfavorable prognosis: an immunohistochemical study. Thyroid 2002; 12: 747-754.
  • 19 Szanto J, Vincze B, Sinkovics I. et al. Postoperative thyroglobulin level determination to follow up patients with highly differentiated thyroid cancer. Oncology 1989; 46: 99-104.
  • 20 Tylski P, Stute S, Grotus N. et al. Comparative assessment of methods for estimating tumor volume and standardized uptake value in 18F-FDG PET. J Nucl Med 2010; 51: 268-276.
  • 21 Vera P, Kuhn-Lansoy C, Edet-Sanson A. et al. Does recombinant human thyrotropin-stimulated positron emission tomography with [18F]fluoro-2-deoxy-D-glucose improve detection of recurrence of well-differentiated thyroid carcinoma in patients with low serum thyroglobulin?. Thyroid 2010; 20: 15-23.
  • 22 Wang W, Larson SM, Fazzari M. et al. Prognostic value of (18F) fluorodeoxyglucose positron emission tomographic scanning in patients with thyroid cancer. J Clin Endocrinol Metab 2000; 85: 1107-1113.