Use of Recombinant Human Thyrotropin before Radioiodine Therapy in Patients with Advanced Differentiated Thyroid Carcinoma
M. Luster,
M. Lassmann,
H. Haenscheid,
U. Michalowski,
C. Incerti and
C. Reiners
Department of Nuclear Medicine, University of Wuerzburg (M.L.,
M.L., H.H., U.M., C.R.), D-97080 Wuerzburg, Germany; and Genzyme
Europe, 1411 DD Naarden, The Netherlands
Address all correspondence and requests for reprints to: Dr. M. Luster, Department of Nuclear Medicine, University of Wuerzburg, Josef-Schneider-Str. 2, D-97080 Wuerzburg, Germany. E-mail:
luster{at}nuklearmedizin.uni-wuerzburg.de
The use of 131I for radioablative therapy in patients with
differentiatedthyroid cancer (DTC) requires a sufficient serum
concentrationof TSH for efficient thyroid tissue uptake of iodine. We
describethe use of recombinant human TSH (rhTSH) in conjunction with
ablativeradioiodine therapy (RIT) in 11 patients (16 total treatments)
withadvanced and/or recurrent DTC (5 papillary, 6 follicular) forwhom
withdrawal of thyroid hormone suppression therapy (THST),the standard
method to increase serum TSH, was not an option.Indications for rhTSH
use in these patients included inabilityto tolerate withdrawal of
thyroid hormones due to very poorphysical condition or inability to
achieve sufficient serumTSH levels after THST withdrawal. Ten patients
had undergonethyroidectomy, and most (9 of 11) had received prior
ablativeRIT after THST withdrawal. Baseline thyroglobulin levels
rangedfrom 25 to nearly 30,000 ng/mL, reflecting the heterogeneityof
the patient population. In 7 cases (5 patients), posttherapy
thyroglobulinlevels assessed at a mean of 4.3 months (range, 210
months)after 131I therapy were decreased by at least 30%
compared topretherapy levels. In follow-up visits, an additional 3
patientsshowed marked clinical improvement or decreased or stabilized
tumorburden in whole body scans compared to pretherapy scans. Three
patientsdied of progressive disease within 2 months of therapy before
follow-upassessments occurred. No adverse events were reported among
the8 surviving patients. The results suggest that rhTSH offersa
promising alternative to THST withdrawal to allow ablativeRIT after
effective TSH stimulation in patients with advancedrecurrent DTC who
would not otherwise be able to receive thistreatment. This therapeutic
indication extends the clinicalpotential of this new agent, already
demonstrated to be effectivefor use with 131I for
diagnostic purposes.
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