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甲状腺癌:基于实际生物动力学测量的 131I 治疗中的辐射安全预防措施。

Thyroid cancer: radiation safety precautions in 131I therapy based on actual biokinetic measurements.

机构信息

From the Department of Nuclear Medicine, West China Hospital, Sichuan University, 37 Guoxue Alley, Chengdu 610041, China.

出版信息

Radiology. 2014 Oct;273(1):211-9. doi: 10.1148/radiol.14132234. Epub 2014 Jun 5.

Abstract

PURPOSE

To formulate radiation precautions for patients with thyroid cancer who are undergoing thyroid hormone withdrawal-induced hypothyroidism and iodine 131 ((131)I) therapy through actual biokinetic measurements.

MATERIALS AND METHODS

Informed consent and institutional review board approval were obtained. From October 2008 to December 2011, consecutive patients with differentiated thyroid cancer who had been prepared for (131)I ablation treatment or (131)I treatment for metastatic disease during follow-up were prospectively recruited. Calculations based on deduced whole-body retention and measured iodine biokinetics in thyroidal tissue were derived to determine the thyroidal and extrathyroidal compartment uptake fractions and effective half-lives. Precaution times necessary to avoid close contact with family members and the general public were derived from these parameters and regulatory dose limits.

RESULTS

Seventy-seven patients (36 with ablation treatments, 41 with follow-up treatments) were eligible for the analysis. Actual dose rates from patients after therapeutic (131)I administration were greatly lower than those described in the American Thyroid Association (ATA) and Nuclear Regulatory Commission (NRC) models: The mean initial dose rate at 0.3 m for patients with ablation treatment was only 28% (0.183/0.655 µSv/h/MBq) ± 2.9 (standard deviation) (range, 12.1%-38.3%) and 36% (0.183/0.511 µSv/h/MBq) ± 3.7 (range, 15.5%-49.1%) of that described in the NRC and ATA models, respectively; the equivalent values for patients with follow-up treatment were only 30% (0.195/0.655 µSv/h/MBq) ± 3.5 (range, 12.5%-45.3%) and 38% (0.195/0.511 µSv/h/MBq) ± 4.5 (range, 16.0%-58.1%), respectively. The actual mean effective (131)I half-life in the thyroid remnant tissue was greatly lower than that described in the ATA and NRC models: 47.6 versus 175.2 hours.

CONCLUSION

On the basis of the current dose limits, typically administered activities of 3.7 GBq to a patient with ablation treatment or 7.4 GBq to a patient with follow-up treatment required 3 days of sleeping apart for keeping the doses to pregnant women and children below 1 mSv. No precautions were required for non-cosleeping nonpregnant adult family members.

摘要

目的

通过实际生物动力学测量,为接受甲状腺激素抑制诱导性甲状腺功能减退和碘 131((131)I)治疗的甲状腺癌患者制定辐射防护措施。

材料和方法

获得知情同意和机构审查委员会批准。从 2008 年 10 月至 2011 年 12 月,连续招募了接受放射性碘 ((131)I)消融治疗或随访期间转移性疾病 ((131)I)治疗的分化型甲状腺癌患者。基于推导出的全身保留和测量的甲状腺组织碘生物动力学,计算甲状腺和甲状腺外腔摄取分数和有效半衰期。从这些参数和监管剂量限制中得出避免与家庭成员和公众密切接触所需的预防时间。

结果

77 名患者(36 名接受消融治疗,41 名接受随访治疗)符合分析条件。治疗后 ((131)I 给予患者的实际剂量率远低于美国甲状腺协会 (ATA)和核监管委员会 (NRC)模型中描述的剂量率:消融治疗患者的 0.3 m 处初始平均剂量率仅为 28%(0.183/0.655 µSv/h/MBq)±2.9(标准差)(范围,12.1%-38.3%)和 36%(0.183/0.511 µSv/h/MBq)±3.7(范围,15.5%-49.1%)分别为 NRC 和 ATA 模型中描述的剂量率;随访治疗患者的等效值分别仅为 30%(0.195/0.655 µSv/h/MBq)±3.5(范围,12.5%-45.3%)和 38%(0.195/0.511 µSv/h/MBq)±4.5(范围,16.0%-58.1%)。甲状腺残留组织中实际有效 ((131)I 半衰期远低于 ATA 和 NRC 模型中描述的半衰期:47.6 小时与 175.2 小时。

结论

根据当前的剂量限制,对接受消融治疗的患者通常给予 3.7GBq 的活动度,对接受随访治疗的患者给予 7.4GBq 的活动度,需要 3 天的分开睡眠,以使孕妇和儿童的剂量低于 1mSv。对于非同睡的非孕妇成年家庭成员,无需采取任何预防措施。

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