Zusammenfassung
Thyreoglobulin (hTg) bzw. Kalzitonin (hCt) sind etablierte humorale Tumormarker für
die Therapieüberwachung und Nachsorge der behandelten thyreoidalen Follikelzell- bzw.
C-Zell-Karzinome. Hierfür besitzen diese Analyten eine im Vergleich zu vielen anderen
Tumormarkern hohe diagnostische Spezifität, die mit dem Ausmaß der Radikalität der
Schilddrüsenablation zunimmt. In den letzten Jahren werden Assays mit zunehmender
funktioneller Sensitivität angeboten, die allerdings mit neuen Herausforderungen an
die labortechnische Durchführung, die Qualitätssicherung sowie die Interpretation
der im „ultrasensitiven” Bereich messbaren Werte einhergehen. Ohnehin sind hTg und
hCt als relativ anspruchsvolle Laborparameter anzusehen. Die Messergebnisse sind zum
Teil deutlich abhängig von diversen In-vivo- und In-vitro-Einflussfaktoren, aber auch
bei konstanten Rahmenbedingungen ist die Vergleichbarkeit der gemessenen Werte zwischen
verschiedenen Assays nicht ohne weiteres garantiert. Hinsichtlich der hCt-Bestimmung
bieten Assays mit weitgehend selektiver Erfassung der monomeren (reifen) Kalzitoninform
den Vorteil einer weiteren Steigerung der diagnostischen Spezifität. Abgesehen von
der Überwachung der wegen eines Schilddrüsenkarzinom behandelten Patienten wird die
hCt-Bestimmung von zahlreichen Fachgesellschaften auch bei der Dignitätsabklärung
thyreoidaler Raumforderungen als gerechtfertigt angesehen, wohingegen die hTg-Bestimmung
nicht als Routinemaßnahme zur Schilddrüsenknotenabklärung in die Leitlinien aufgenommen
wurde. Die hTg-Bestimmung kann aber bei der Evaluierung bestimmter benigner Schilddrüsenprozesse
indiziert sein wie der Differenzialdiagnose der konnatalen Hypothyreose, der Abklärung
einer vermuteten faktitiellen Hyperthyreose oder als Aktivitätsmarker für destruierende
Schilddrüsenprozesse wie der subakuten oder Amiodaron-induzierten Thyreoiditis.
Abstract
Thyroglobulin and calcitonin are established humoral tumor markers for therapy monitoring
and follow up of thyroid cancer of follicular origin or medullary thyroid cancer,
respectively. In comparison to many other tumor markers these analytes offer a high
diagnostic specificity, which increases with the radicalness of thyroid ablation.
Over the last years, assays with rising functional sensitivity became commercially
available, being however a challenge in respect to laboratory performance, quality
assurance and medical judgement in the „ultrasensitive” range of detectable concentrations.
Anyway, hTg and hCT must be considered to be ambitious laboratory parameters. The
results considerably depend on various in vivo and in vitro influences, and even under
constant conditions, different assays may not necessarily produce identical results.
hCt assays that measure the monomer (mature) calcitonin form have the advantage of
an enhancement of the diagnostic specificity. Apart from follow up investigations
in treated MTC patients, a couple of medical societies assume hCt measurement to be
justified in the presence of a thyroid nodule. In contrast, guidelines do not recommend
hTg measurement as a routine procedure for the assessment of the malignancy of thyroid
nodules. However, hTg measurement may have an indication in differential diagnosis
of connatal hypothyroidism, in assumed thyrotoxicosis factitia and as a marker of
destructive thyroidal disease like subacute or amiodarone-induced thyroiditis.
Schlüsselwörter
Thyreoglobulin (hTg) - Kalzitonin (hCt) - differenziertes Schilddrüsenkarzinom - medulläres
Schilddrüsenkarzinom - Nachsorge - Schilddrüsenknoten
Key words
thyroglobulin (hTg) - calcitonin (hCt) - differentiated thyroid cancer - medullary
thyroid cancer - restaging - thyroid nodule
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PD Dr. Rainer Görges
Klinik für Nuklearmedizin
Universitätsklinikum Essen
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