Judicious use of recombinant TSH in the management of differentiated thyroid carcinoma
Objective To evaluate the feasibility of using recombinant human TSH (rhTSH) in conjunction with 131 I to treat patients with differentiated thyroid carcinoma. Methods Between July 2003 and April 2009, 14 patients [mean age, 39.1 years (range 14–71 years)], of whom seven were treated for remnant abl...
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Veröffentlicht in: | Annals of nuclear medicine 2010-10, Vol.24 (8), p.609-615 |
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Sprache: | eng |
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Zusammenfassung: | Objective
To evaluate the feasibility of using recombinant human TSH (rhTSH) in conjunction with
131
I to treat patients with differentiated thyroid carcinoma.
Methods
Between July 2003 and April 2009, 14 patients [mean age, 39.1 years (range 14–71 years)], of whom seven were treated for remnant ablation and seven for irresectable or metastatic disease, received rhTSH-aided
131
I therapy. None had an adequate rise in TSH. The mean
131
I dosage administered was 5206.3 MBq. Baseline thyroglobulin/anti-thyroglobulin (Tg/anti-Tg) and TSH levels were documented. rhTSH (0.9 mg) was given intramuscularly on days 1 and 2, and TSH levels were recorded.
131
I was given when the TSH level rose to >30 μIU/ml. Tg/anti-Tg levels were measured at 3-month intervals. A
131
I whole-body scan (
131
I scan) was performed 6 or 12 months after treatment.
Results
The baseline median valid Tg and TSH levels were 76.2 ng/ml (range 14.1 to >30000) and 3.63 μIU/ml (range 1.36–11.0), respectively. The rise in TSH level was 34.8–96.9 μIU/ml after the first rhTSH injection and 33.1 to >75 μIU/ml after the second injection. The post-therapy
131
I scan showed uptake at disease sites in all patients, indicating the initial empirical adequacy of treatment. Follow-up
131
I scan was positive for four patients, but negative for three of these patients after subsequent therapy. Complete resolution of disease was seen in eight patients and partial resolution in four after 3 months of therapy; one had stable disease; and in one patient with progressive disease, complete resolution was achieved after repeated
131
I doses with thyroxine withdrawal. After a median follow-up of 39.2 months, all patients were alive and no disease recurrence was observed. The overall response rate at 3 months was 86% and had improved to 93% at the time of this review. The final ablation rate in seven patients was 100%. Apart from notable neck swelling in four patients, which was responsive to medication, and headache in two patients, no significant short-term side-effects of therapy were seen.
Conclusion
In our setting, the use of rhTSH-aided
131
I ablation and treatment was safe and effective. |
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ISSN: | 0914-7187 1864-6433 |
DOI: | 10.1007/s12149-010-0404-8 |