Wang Junyao, Zhang Ke, He Ziyan, Chai Hong, Yang Jiahuan, Zhong Peng, Chen Zequan, Chen Libo
Department of Nuclear Medicine, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Nucl Med Commun. 2025 Sep 1;46(9):793-800. doi: 10.1097/MNM.0000000000002006. Epub 2025 Jun 30.
Radioiodine ( 131 I) remnant ablation (RRA) with activities ranging from 1.1-3.7 GBq showed dismal efficacy but a dose-effect relationship in patients with differentiated thyroid cancer (DTC) after less-than-total thyroidectomy.
A prospective study was conducted in patients with DTC with gross thyroid remnants. All subjects received an activity of 5.55 GBq of 131 I in combination with a 1-week course of prednisone at a dose of 60 mg/day. The primary endpoints included success rate and safety; secondary endpoints included changes in 131 I uptake value, gross thyroid remnant volume, serum thyroglobulin levels, and levothyroxine replacement dose.
Forty-two patients were eligible for analyses with a median follow-up of 35 months. The ablation success rate reached 95.2%, with all grade 1 adverse events. The incidence of long-term (11.9%) adverse events was significantly lower than intermediate (28.6%) and immediate (69.0%) ones. The most frequent treatment-related immediate adverse events included neck pain (54.8%), weakness (30.1%), neck swelling (23.8%), stomachache (21.4%), palpitation (16.7%), and nausea (9.5%). After RRA, the median 24-h 131 I uptake value and the thyroid remnant volume decreased significantly ( P < 0.05). The thyrotropin-stimulated thyroglobulin level dropped remarkably (20.54 ± 21.58 vs. 1.54 ± 3.21 mIU/L; P < 0.05), becoming undetectable in 11 (28.9%) patients; While the dose of administered levothyroxine enhanced notably ( P = 0.033).
Our data demonstrated that prednisone-aided RRA utilizing a single dose of 5.55 GBq of 131 I achieved a high success rate of 95.2% and an excellent safety profile in patients with DTC with gross thyroid remnant.
对于甲状腺次全切除术后的分化型甲状腺癌(DTC)患者,使用1.1 - 3.7 GBq活度的放射性碘(131I)进行残余甲状腺组织消融(RRA)疗效不佳,但存在剂量效应关系。
对有肉眼可见甲状腺残余组织的DTC患者进行了一项前瞻性研究。所有受试者接受5.55 GBq的131I,并联合服用为期1周、剂量为60 mg/天的泼尼松。主要终点包括成功率和安全性;次要终点包括131I摄取值、甲状腺残余组织体积、血清甲状腺球蛋白水平及左甲状腺素替代剂量的变化。
42例患者符合分析条件,中位随访时间为35个月。消融成功率达到95.2%,所有不良事件均为1级。长期不良事件的发生率(11.9%)显著低于中期(28.6%)和即刻(69.0%)不良事件。最常见的与治疗相关的即刻不良事件包括颈部疼痛(54.8%)、乏力(30.1%)、颈部肿胀(23.8%)、腹痛(21.4%)、心悸(16.7%)和恶心(9.5%)。RRA后,24小时131I摄取值中位数及甲状腺残余组织体积显著下降(P < 0.05)。促甲状腺素刺激后的甲状腺球蛋白水平显著下降(20.54 ± 21.58 vs. 1.54 ± 3.21 mIU/L;P < 0.05),11例(28.9%)患者降至检测不到水平;而左甲状腺素的给药剂量显著增加(P = 0.033)。
我们的数据表明,对于有肉眼可见甲状腺残余组织的DTC患者,使用单剂量5.55 GBq的131I并辅助泼尼松进行RRA,成功率高达95.2%,且安全性良好。