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Journal of Clinical Endocrinology & Metabolism, doi:10.1210/jc.2004-1550
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The Journal of Clinical Endocrinology & Metabolism Vol. 90, No. 1 79-83
Copyright © 2005 by The Endocrine Society

Recombinant Human Thyrotropin Markedly Changes the 131I Kinetics during 131I Therapy of Patients with Nodular Goiter: An Evaluation by a Randomized Double-Blinded Trial

Viveque Egsgaard Nielsen, Steen Joop Bonnema, Henrik Boel-Jørgensen, Annegrete Veje and Laszlo Hegedüs

Departments of Endocrinology and Metabolism (V.E.N., S.J.B., L.H.) and Nuclear Medicine (H.B.-J., A.V.), Odense University Hospital, DK-5000 Odense, Denmark

Address all correspondence and requests for reprints to: Viveque Egsgaard Nielsen, M.D., Department of Endocrinology and Metabolism, Odense University Hospital, DK-5000 Odense C, Denmark. E-mail: viveque.egsgaard{at}ouh.fyns-amt.dk.

The present study compares, in a randomized double-blinded design, the expected and the actual absorbed thyroid radioactive dose in response to 0.3 mg recombinant human (rh)TSH (n = 35) or placebo (n = 28) given 24 h before 131I therapy in patients with nodular goiter (median volume, 69 ml; range, 20–440 ml). The 131I activity calculation was based on thyroid 131I uptake (RAIU) at 24 and 96 h after a tracer dose of 0.5 MBq 131I. After 131I therapy, 24- and 96-h RAIU were repeated allowing a more exact assessment of the actual absorbed thyroid dose. The median 131I activity was 617 and 632 MBq, respectively, in the rhTSH and the placebo group. At baseline, the 24- and 96-h RAIU and the expected thyroid dose were 32.8 ± 9.1%, 32.1 ± 8.2%, and 96.3 ± 16.3 Gy, respectively, in the rhTSH group and 35.7 ± 11.8%, 35.2 ± 11.3%, and 94.1 ± 18.5 Gy, respectively, in the placebo group (P value not significant between groups). After 131I therapy, the 24- and 96-h RAIU and the actual absorbed thyroid dose were 46.9 ± 11.7%, 45.0 ± 12.1%, and 136.7 ± 47.9 Gy, respectively, in the rhTSH group and 33.0 ± 11.4%, 31.0 ± 11.3%, and 76.9 ± 27.5 Gy, respectively, in the placebo group (P < 0.001 between groups). Comparing the expected with the actual absorbed thyroid dose, this corresponds to a mean increase of 36.4% (95% confidence interval, 21.3–53.4) in the rhTSH group and a decrease of 21.5% (95% confidence interval, –33.9 to –6.6) in the placebo group (P < 0.001), equivalent to an increase of 73.8% in the absorbed thyroid dose in the rhTSH-treated group. We have thus for the first time shown that stimulation with rhTSH before 131I therapy not only hinders the decrease in the thyroid RAIU observed with conventional 131I therapy but in fact also significantly enhances the absorbed thyroid dose. Whether this also leads to a significant increase in goiter size reduction needs additional study.




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