Pitié-Salpêtrière Hospital, Sorbonne Université, Paris, France.
Gustave Roussy, Univ. Paris Saclay, Villejuif, France.
J Clin Endocrinol Metab. 2019 Apr 1;104(4):1020-1028. doi: 10.1210/jc.2018-01589.
Recombinant human thyrotropin (rhTSH) has been shown to be an effective stimulation method for radioactive iodine (RAI) therapy in differentiated thyroid cancer, including in those with nodal metastases (N1 DTC).
To demonstrate the noninferiority of rhTSH vs thyroid hormone withdrawal (THW) in preparation to RAI regarding disease status at the first evaluation in the real-life setting in patients with N1 DTC.
This was a French multicenter retrospective study. Groups were matched according to age (<45/≥45 years), number of N1 nodes (≤5/>5 lymph nodes), and stage (pT1-T2/pT3).
The cohort consisted of 404 patients pT1-T3/N1/M0 DTC treated with rhTSH (n = 205) or THW (n = 199). Pathological characteristics and initially administrated RAI activities (3.27 ± 1.00 GBq) were similar between the two groups. At first evaluation (6 to 18 months post-RAI), disease-free status was defined by thyroglobulin levels below threshold and a normal ultrasound. Disease-free rate was not inferior in the rhTSH group (75.1%) compared with the THW group (71.9%). The observed difference between the success rates was 3.3% (-6.6 to 13.0); rhTSH was therefore considered noninferior to THW because the upper limit of this interval was <15%. At the last evaluation (29.7 ± 20.7 months for rhTSH; 36.7 ± 23.8 months for THW), 83.5% (rhTSH) and 81.5% (THW) of patients achieved a complete response. This result was not influenced by any of the known prognostic factors.
A preparation for initial RAI treatment with rhTSH was noninferior to that with THW in our series of pT1-T3/N1/M0-DTC on disease-free status outcomes at the first evaluation and after 3 years.
重组人促甲状腺激素(rhTSH)已被证明是分化型甲状腺癌放射性碘(RAI)治疗的有效刺激方法,包括有淋巴结转移(N1 DTC)的患者。
在有 N1 DTC 的患者中,在真实环境中,与甲状腺激素停药(THW)相比,rhTSH 作为 RAI 准备的非劣效性,证明其在首次评估时疾病状态的非劣效性。
这是一项法国多中心回顾性研究。根据年龄(<45/≥45 岁)、N1 节点数(≤5/>5 个淋巴结)和分期(pT1-T2/pT3),对两组进行匹配。
该队列包括 404 名接受 rhTSH(n = 205)或 THW(n = 199)治疗的 pT1-T3/N1/M0 DTC 患者。两组的病理特征和最初给予的 RAI 活性(3.27±1.00GBq)相似。在首次评估(RAI 后 6 至 18 个月)时,通过甲状腺球蛋白水平低于阈值和正常超声定义无疾病状态。rhTSH 组的无疾病率(75.1%)不低于 THW 组(71.9%)。观察到的成功率差异为 3.3%(-6.6 至 13.0);因此,rhTSH 被认为不劣于 THW,因为该区间的上限<15%。在最后一次评估时(rhTSH 为 29.7±20.7 个月;THW 为 36.7±23.8 个月),83.5%(rhTSH)和 81.5%(THW)的患者获得完全缓解。该结果不受任何已知预后因素的影响。
在我们的 pT1-T3/N1/M0-DTC 系列中,与 THW 相比,rhTSH 用于初始 RAI 治疗的准备在首次评估和 3 年后的无疾病状态结果方面非劣效。