Mariani G, Ferdeghini M, Augeri C, Villa G, Taddei G Z, Scopinaro G, Boni G, Bodei L, Rabitti C, Molinari E, Bianchi R
Nuclear Medicine Service, DIMI, Univ of Genoa, Italy.
Cancer Biother Radiopharm. 2000 Apr;15(2):211-7. doi: 10.1089/cbr.2000.15.211.
The purpose of this work was to gain clinical experience with and to identify the optimal conditions for the use of recombinant human TSH (rhTSH, commercially available as Thyrogen) in the management of patients with differentiated thyroid cancer (DTC). The study involved 22 patients for a total of 27 administration cycles of rhTSH, for either diagnostic (in 19 instances) and/or therapeutic purposes (in 8 instances). There were 19 patients with papillary cancer (follicular variant in 4, columnar variant in 1) and 3 patients with follicular cancer (1 Hurtle cell variant). All patients had previously undergone total thyroidectomy and 1-5 cycles of 131I-therapy. Thyrogen was administered i.m. according to the suggested protocol: 0.9 mg i.m. on days 1 and 2, radioiodine on day 3. Peak serum TSH levels between 68-237 microIU/mL were observed after rhTSH administration; these were on average 65% higher, on a patient-by-patient basis, than peak serum TSH observed after conventional withdrawal of thyroxine treatment in 19 patients, while in 3 patients they were 28% lower, but still in the potent stimulation range (86-94 microIU/mL). There was general agreement between imaging results obtained under rhTSH stimulation and those obtained on prior occasions during thyroxine withdrawal, although radioiodine uptake was interpreted as less intense following Thyrogen administration. Of 18 patients undergoing rhTSH administration for diagnostic purposes, 11 patients had a negative radioiodine whole-body scan (WBS) and 7 had a positive WBS. Three of the WBS-negative patients were shown to be actually affected by tumor recurrence, respectively by PET with [18F]FDG (in 2 cases) and by post-131I therapy scan. Serum thyroglobulin (hTg) increased to abnormal levels following rhTSH stimulation in 3/7 of the WBS-positive patients as well as in 1/11 WBS-negative patients. In 3/7 WBS-positive as well as in 3/11 WBS-negative patients, serum hTg progressively rose under rhTSH stimulation, yet still remaining below 3 ng/mL. Post-131I therapy scans following Thyrogen administration showed good radioiodine uptake in 7/8 patients, the single unsuccessful case being most likely due to expansion of the iodine pool because of recent use of an iodinated contrast medium. The overall results show the feasibility and practical advantages of employing rhTSH stimulation in the general clinical setting rather than thyroxine withdrawal in the management of DTC patients. Caution should be raised on the interpretation of the serum hTg response to such potent but short-lived TSH stimulation.
本研究旨在获取使用重组人促甲状腺素(rhTSH,商品名为Thyrogen)治疗分化型甲状腺癌(DTC)患者的临床经验,并确定其最佳使用条件。该研究纳入了22例患者,共进行了27个rhTSH给药周期,用于诊断(19例)和/或治疗目的(8例)。其中19例为乳头状癌患者(4例为滤泡状亚型,1例为柱状亚型),3例为滤泡状癌患者(1例为许特耳细胞亚型)。所有患者均已接受甲状腺全切术及1 - 5个周期的131I治疗。按照推荐方案进行肌肉注射Thyrogen:第1天和第2天各注射0.9 mg,第3天注射放射性碘。注射rhTSH后,血清促甲状腺素(TSH)峰值水平在68 - 237 μIU/mL之间;与19例患者常规停用甲状腺素治疗后观察到的血清TSH峰值相比,逐个患者计算平均高出65%,而3例患者的TSH峰值虽低28%,但仍处于有效刺激范围内(86 - 94 μIU/mL)。rhTSH刺激下获得的影像学结果与之前停用甲状腺素期间获得的结果总体一致,尽管Thyrogen给药后放射性碘摄取被认为强度较低。在18例接受rhTSH诊断性给药的患者中,11例患者的放射性碘全身扫描(WBS)为阴性,7例为阳性。3例WBS阴性患者经证实实际上存在肿瘤复发,分别通过[18F]FDG PET(2例)和131I治疗后扫描发现。在7例WBS阳性患者中的3例以及11例WBS阴性患者中的1例中,rhTSH刺激后血清甲状腺球蛋白(hTg)升高至异常水平。在7例WBS阳性患者中的3例以及11例WBS阴性患者中的3例中,rhTSH刺激下血清hTg逐渐升高,但仍低于3 ng/mL。Thyrogen给药后进行的131I治疗后扫描显示,8例患者中有7例放射性碘摄取良好,唯一未成功的病例很可能是由于近期使用了碘化造影剂导致碘池扩大。总体结果表明,在DTC患者管理中,采用rhTSH刺激而非停用甲状腺素具有可行性和实际优势。对于血清hTg对这种强效但短暂的TSH刺激的反应解释应谨慎。