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Nuclear Medicine Department, Warren Grant Magnuson Clinical Center (S.-S.K., J.C.R., A.M.K.), and the Clinical Endocrinology (E.G.M., K.B.A., M.C.L., J.R.) and Genetics and Biochemistry Branchs, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892
Address all correspondence and requests for reprints to: James C. Reynolds, M.D., Building 10, Room 1C-401, National Institutes of Health, Bethesda, Maryland 20892.
As lithium inhibits the release of iodine from the thyroid but does not
change iodine uptake, it may potentiate 131I therapy of
thyroid cancer. The effects of lithium on the accumulation and
retention of 131I in metastatic lesions and thyroid
remnants were evaluated in 15 patients with differentiated thyroid
carcinoma. Two 131I turnover studies were performed while
the patients were hypothyroid. One was performed while the patient
received lithium; the second served as a control study. From a series
of
-camera images, it was found that lithium increased
131I retention in 24 of 31 metastatic lesions and in 6 of 7
thyroid remnants. A comparison of 131I retention during
lithium with that during the control period showed that the mean
increase in the biological or retention half-life was 50% in tumors
and 90% in remnants. This increase occurred in at least 1 lesion in
each patient and was proportionally greater in lesions with poor
131I retention. When the control biological half life was
less than 3 days, lithium prolonged the effective half-life, which
combines both biological turnover and isotope decay, in responding
metastases by more than 50%. More 131I also accumulated
during lithium therapy, probably as a consequence of its effect on
iodine release. The increase in the accumulated 131I and
the lengthening of the effective half-life combined to increase the
estimated 131I radiation dose in metastatic tumor by
2.29 ± 0.58 (mean ± SEM) times. These studies
suggest that lithium may be a useful adjuvant for 131I
therapy of thyroid cancer, augmenting both the accumulation and
retention of 131I in lesions.
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