Kobe Carsten, Eschner Wolfgang, Wild Markus, Rahlff Ilka, Sudbrock Ferdinand, Schmidt Matthias, Dietlein Markus, Schicha Harald
Department of Nuclear Medicine, University of Cologne, Cologne D-50924, Germany.
Nucl Med Commun. 2010 Mar;31(3):201-5. doi: 10.1097/MNM.0b013e328333d303.
The use of radioiodine therapy is common in the treatment of benign thyroid disease. Council directive Euratom 97/43 requires that for all medical exposure of individuals for radiotherapeutic purposes exposures of target volumes should be individually planned. There are several strategies to accomplish this aim for radioiodine therapy including individual radioiodine uptake measurement and using either individual or mean effective radioiodine uptake and half-life. Although it is always simple to use standard activities, the effective thyroidal half-life and thyroidal uptake of I needs to be estimated individually to achieve optimal dosimetric results. We analyzed the radioiodine half-life and uptake in a large number of patients for use in a semi-individual calculation.
Patients presenting consecutively between 1 January 2006 and 31 December 2007 were included in the study. Inclusion criteria were the control of hyperthyroidism and withdrawal of antithyroid drugs 2 days before preliminary radioiodine testing and therapy. Patients were treated for Graves' disease (n=363), nontoxic goitre (n=50), toxic goitre (n=639), or toxic uninodular adenoma (n=365). The effective half-life and uptake of I were estimated by uptake measurements after 24 h and 5 days during the preliminary radioiodine test, and serial measurements over 5 days during therapy.
The mean effective half-life of I measured during radioiodine therapy was 5.4 days in Graves' disease, 6.4 days in nontoxic goitre, 6.6 days in toxic goitre, and 5.7 days in toxic uninodular adenoma. The mean maximal uptake of I measured during radioiodine therapy was 64% in Graves' disease, 42% in nontoxic goitre, 38% in toxic goitre, and 31% in toxic uninodular adenoma.
These actual values analyzed here might be used for a semi-individual calculation of therapeutic activity when an individual approach is not possible.
放射性碘治疗常用于良性甲状腺疾病的治疗。欧洲原子能共同体理事会指令97/43要求,对于所有因放射治疗目的对个体进行的医疗照射,靶区的照射应进行个体化规划。实现放射性碘治疗这一目标有多种策略,包括个体放射性碘摄取测量以及使用个体或平均有效放射性碘摄取量和半衰期。尽管使用标准活度总是很简单,但为了获得最佳剂量学结果,需要分别估计碘的有效甲状腺半衰期和甲状腺摄取量。我们分析了大量患者的放射性碘半衰期和摄取量,用于半个体化计算。
纳入2006年1月1日至2007年12月31日期间连续就诊的患者。纳入标准为甲状腺功能亢进得到控制且在初步放射性碘检测和治疗前2天停用抗甲状腺药物。患者接受格雷夫斯病(n = 363)、非毒性甲状腺肿(n = 50)、毒性甲状腺肿(n = 639)或毒性单结节腺瘤(n = 365)的治疗。在初步放射性碘检测期间,通过24小时和5天后的摄取测量估计碘的有效半衰期和摄取量,并在治疗期间进行5天的连续测量。
放射性碘治疗期间测得的碘平均有效半衰期在格雷夫斯病中为5.4天,在非毒性甲状腺肿中为6.4天,在毒性甲状腺肿中为6.6天,在毒性单结节腺瘤中为5.7天。放射性碘治疗期间测得的碘平均最大摄取率在格雷夫斯病中为64%,在非毒性甲状腺肿中为42%,在毒性甲状腺肿中为38%,在毒性单结节腺瘤中为31%。
当无法采用个体化方法时,此处分析的这些实际值可用于治疗活度的半个体化计算。