Bal C, Padhy A K, Jana S, Pant G S, Basu A K
Department of Nuclear Medicine, All India Institute of Medical Sciences, New Delhi.
Cancer. 1996 Jun 15;77(12):2574-80. doi: 10.1002/(SICI)1097-0142(19960615)77:12<2574::AID-CNCR22>3.0.CO;2-O.
Radioiodine has been used for more than a half-century to ablate thyroid remnants following thyroid surgery, but a single optimal dose has not been established. We designed a prospective randomized trial to determine the optimal dose of 131 I for remnant ablation.
Using a simple randomization technique, 149 patients with remnant thyroid were incorporated into 4 treatment groups. Twenty-seven of these patients were administered 25 to 34 millicurie (mCi) of 131 I (30 +/- 1.5), 54 received 35 to 64 mCi (50.6 +/- 5.4), 38 received 65 to 119 mCi (88.6 +/- 14) and 30 patients received 120 to 200 mCi (155 +/- 28.7). Six months to 1 year after treatment, all subjects were reassessed after withdrawing L-thyroxine for 4 to 6 weeks. A successful ablation was defined as the absence of thyroid bed activity in 5 mCi 131 I neck scan at 48 hours along with 2 adjunctive criteria which were the neck uptake of <0.2% of the administered activity and the thyroglobulin (Tg) value of <10 ng/mL.
Applying the above criteria, we observed complete ablation of 17 of 27 thyroid gland remnants (63%) in the 30 mCi group, 42 of 54 (77.8%) in the 50 mCi group, 28 of 38 (73.7%) in the 90 mCi group and 23 of 30 (76.7%) in the 155 mCi group. When the radiation-absorbed dose was calculated, a 30 mCi dose delivered approximately 20,000 centigray (cGy), a 50 mCi dose about 30,000 cGy, a 90 mCi dose about 50,000 cGy, and a 155 mCi dose about 130,000 cGy.
Increasing the empirical 131 I initial dose to more than 50 mCi results in plateauing of the dose-response curve and thus, conventional high dose remnant ablation needs critical evaluation. Based on dosimetry results, one should aim to deliver about 30,000 cGy to the thyroid remnant, as higher doses do not appear to yield a higher ablation rate.
放射性碘已用于甲状腺手术后消融甲状腺残余组织半个多世纪,但尚未确定单一的最佳剂量。我们设计了一项前瞻性随机试验,以确定用于残余组织消融的131I最佳剂量。
采用简单随机化技术,将149例有甲状腺残余组织的患者纳入4个治疗组。其中27例患者接受25至34毫居里(mCi)的131I(30±1.5),54例接受35至64 mCi(50.6±5.4),38例接受65至119 mCi(88.6±14),30例患者接受120至200 mCi(155±28.7)。治疗后6个月至1年,所有受试者在停用左旋甲状腺素4至6周后重新评估。成功消融的定义为48小时时5 mCi 131I颈部扫描甲状腺床无活性,以及另外两个辅助标准,即颈部摄取量<给药活性的0.2%和甲状腺球蛋白(Tg)值<10 ng/mL。
应用上述标准,我们观察到30 mCi组27个甲状腺残余组织中有17个(63%)完全消融,50 mCi组54个中有42个(77.8%),90 mCi组38个中有28个(73.7%),155 mCi组30个中有23个(76.7%)。计算辐射吸收剂量时,30 mCi剂量约为20000厘戈瑞(cGy),50 mCi剂量约为30000 cGy,90 mCi剂量约为50000 cGy,155 mCi剂量约为130000 cGy。
将经验性131I初始剂量增加至50 mCi以上会导致剂量反应曲线趋于平稳,因此,传统的高剂量残余组织消融需要严格评估。基于剂量测定结果,应旨在向甲状腺残余组织给予约30000 cGy的剂量,因为更高的剂量似乎不会产生更高的消融率。