Kukulska Aleksandra, Krajewska Jolanta, Roskosz Józef, Handkiewicz-Junak Daria, Jarzab Michał, Paliczka Ewa, Puch Zbigniew, Wygoda Zbigniew, Gubała Elzbieta, Jarzab Barbara
Department of Nuclear Medicine and Endocrine Oncology Comprehensive Cancer Center and M. Sklodowska-Curie Memorial Institute of Oncology, Branch Gliwice, Gliwice.
Endokrynol Pol. 2006 Jul-Aug;57(4):374-9.
The aim of this study was to compare the early outcomes between two groups of patients with differentiated thyroid carcinoma (DTC) who received 60 or 100 mCi of (131)I for remnant ablation.
224 DTC patients with primary tumor > 1 cm of diameter or multifocal were randomised into prospective clinical trial. Patients with extrathyroideal extension of primary tumor and nodal metastases or M1 were not enrolled. 99 patients received 60 mCi, and 125--100 mCi of radioiodine as the first ablative dose.
The effectiveness of thyroid ablation was evaluated after one year, during endogenous TSH (thyroid stimulating hormone) stimulation, and after two years during Lthyroxine therapy. Whole body scintigraphy (WBS) was performed under thyroxine withdrawal and thyroglobulin serum level was assessed. Distant micrometastases were detected in 9.8% of patients by post-therapy WBS, 11 patients in group A treated with 60 mCi and 11 in group B treated with 100 mCi. In other patients no symptoms of persistent disease were detected. At one year follow up full remission was diagnosed in 176 patients: 76 in group A and 100 in group B. The remaining ones, 13.3% and 11.2% respectively, received the second course of (131)I for remnant ablation. There were no statistically significant differences in Tg (thyroglobulin) serum level either 12 or 24 months after 131I treatment.
Our evaluation of early efficacy of adjuvant radioiodine treatment in low risk DTC patients shows no differences between two radioiodine activities - 60 and 100 mCi in relation to thyroid ablation. Thus, the activity of 60 mCi is recommended.
本研究旨在比较两组分化型甲状腺癌(DTC)患者接受60或100毫居里的(131)I进行残留甲状腺组织消融后的早期疗效。
224例直径大于1厘米或多灶性原发性肿瘤的DTC患者被随机纳入前瞻性临床试验。原发性肿瘤侵犯甲状腺外组织、有淋巴结转移或M1期患者未纳入。99例患者接受60毫居里,125 - 100毫居里放射性碘作为首次消融剂量。
在一年后内源性促甲状腺激素(TSH)刺激期间及两年后左甲状腺素治疗期间评估甲状腺消融效果。在甲状腺素撤药状态下进行全身闪烁扫描(WBS)并评估血清甲状腺球蛋白水平。治疗后WBS在9.8%的患者中检测到远处微转移,A组(接受60毫居里治疗)11例,B组(接受100毫居里治疗)11例。其他患者未检测到持续性疾病症状。在一年随访时,176例患者被诊断为完全缓解:A组76例,B组100例。其余患者分别有13.3%和11.2%接受了第二次(131)I残留甲状腺组织消融治疗。131I治疗后12个月或24个月时血清甲状腺球蛋白(Tg)水平无统计学显著差异。
我们对低风险DTC患者辅助放射性碘治疗早期疗效的评估显示,60和100毫居里这两种放射性碘活度在甲状腺消融方面无差异。因此,推荐60毫居里的活度。