Thyroid Department, Endocrinology Service, Santa Casa de Belo Horizonte, Minas Gerais, Brazil.
Am J Clin Oncol. 2012 Apr;35(2):101-4. doi: 10.1097/COC.0b013e318201a41a.
To evaluate the efficacy of recombinant human thyroid stimulating hormone [rhTSH (versus hypothyroidism)] in thyroid ablation with an activity of 1.1 GBq (30 mCi) (131)I.
A total of 102 patients with thyroid cancer who fulfilled the following criteria were studied: submitted to total thyroidectomy with complete tumor resection; tumor ≤4 cm without extrathyroid invasion or lymph node metastases; negative anti-thyroglobulin (anti-Tg) antibodies. Thirty-two patients (group A) received 0.9 mg of rhTSH for 2 consecutive days followed by (131)I administration and 70 patients (group B) were prepared by levothyroxine withdrawal for 4 weeks. The groups were similar in sex, age, and tumor characteristics.
Ablation was successful (stimulated Tg<1 ng/mL and negative diagnostic whole-body scanning and neck ultrasonography 9 to 12 mo after ablation) in 27 patients of group A (84.3%) and in 58 of group B (83%). Considering patients with Tg greater than 1 ng/mL immediately before (131)I administration, the rates were 72.2% in group A and 75% in group B. In group A, the ablation rate was similar for patients who discontinued levothyroxine-T4 3 days before (131)I administration and those maintained on hormone therapy. The mean follow-up was 29.6 months in group A and 55 months in group B. Stimulated Tg (after rhTSH) was undetectable in 29 patients of group A (90.6%) and in 61 of group B (87%) and 1 patient of group B presented cervical metastases at the last assessment.
Low (131)I activity after rhTSH is effective for remnant ablation in patients who are at low risk of recurrence.
评估 1.1GBq(30mCi)(131)I 活性下重组人促甲状腺激素[rhTSH(与甲状腺功能减退症相比)]在甲状腺消融中的疗效。
研究共纳入 102 例满足以下标准的甲状腺癌患者:接受全甲状腺切除术和完全肿瘤切除术;肿瘤≤4cm 无甲状腺外侵犯或淋巴结转移;抗甲状腺球蛋白(anti-Tg)抗体阴性。32 例患者(A 组)连续 2 天接受 0.9mg rhTSH,然后给予(131)I 治疗,70 例患者(B 组)接受左旋甲状腺素停药 4 周。两组在性别、年龄和肿瘤特征方面相似。
A 组 27 例(84.3%)和 B 组 58 例(83%)患者消融成功(消融后刺激 Tg<1ng/mL,消融后 9-12 个月全身扫描和颈部超声检查阴性)。考虑到(131)I 治疗前即刻 Tg>1ng/mL 的患者,A 组和 B 组的消融率分别为 72.2%和 75%。在 A 组中,停用左甲状腺素-T4 3 天和继续激素治疗的患者消融率相似。A 组的平均随访时间为 29.6 个月,B 组为 55 个月。A 组 29 例(90.6%)和 B 组 61 例(87%)患者的刺激 Tg(rhTSH 后)无法检测到,B 组 1 例患者在最后评估时出现颈部转移。
rhTSH 后低(131)I 活性对复发风险低的患者的残余消融有效。