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分化型甲状腺癌患者术后刺激状态下甲状腺球蛋白水平不可测时的疾病持续存在和复发。

Persistent disease and recurrence in differentiated thyroid cancer patients with undetectable postoperative stimulated thyroglobulin level.

机构信息

Department of Nuclear Medicine and Endocrine Oncology, Institut Gustave Roussy, Univ. Paris-Sud, Villejuif, France.

出版信息

Endocr Relat Cancer. 2011 Mar 3;18(2):R29-40. doi: 10.1677/ERC-10-0292. Print 2011 Apr.

DOI:10.1677/ERC-10-0292
PMID:21183629
Abstract

(131)I is given in differentiated thyroid cancer (DTC) without taking into account thyroglobulin (Tg) levels at the time of ablation, whereas 6-18 months later it is a major criterion for cure. This single-center retrospective study assessed the frequency and risk factors for persistent disease on postablation whole body scan (WBS) and postoperative neck ultrasonography (n-US) and for recurrent disease during the subsequent follow-up, in patients with DTC and undetectable TSH-stimulated Tg level (TSH-Tg) in the absence of Tg antibodies (TgAb) at the time of ablation. Among 1031 patients ablated, 242 (23%) consecutive patients were included. Persistent disease occurred in eight cases (3%) (seven abnormal WBS and one abnormal n-US), all with initial neck lymph node metastases (N1). N1 was a major risk factor for persistent disease. Among 203 patients with normal WBS and a follow-up over 6 months, TSH-Tg 6-18 months after ablation was undetectable in the absence of TgAb in 173 patients, undetectable with TgAb in 1 patient and equal to 1.2  ng/ml in 1 patient. n-US was normal in 152 patients and falsely positive in 3 patients. After a mean follow-up of 4 years, recurrence occurred in two cases (1%), both with aggressive histological variants. The only risk factor for recurrence was an aggressive histological variant (P = 0.03). In conclusion, undetectable postoperative TSH-Tg in the absence of TgAb at the time of ablation is frequent. In these patients, repeating TSH-Tg 6-18 months after ablation is not useful. (131)I ablation could be avoided in the absence of N1 and aggressive histological variant.

摘要

(131)I 治疗仅考虑了消融时的甲状腺球蛋白(Tg)水平,而 6-18 个月后才是治愈的主要标准。这项单中心回顾性研究评估了在消融时 TSH 刺激 Tg 水平(TSH-Tg)无法检测且不存在 Tg 抗体(TgAb)的情况下,DTC 患者行消融术后的全身扫描(WBS)和颈部超声(n-US)检查是否存在持续性疾病,以及在随后的随访中是否存在复发性疾病。在 1031 例接受消融的患者中,连续纳入 242 例患者。8 例(3%)患者发生持续性疾病(7 例 WBS 异常和 1 例 n-US 异常),均存在初始颈部淋巴结转移(N1)。N1 是持续性疾病的主要危险因素。在 203 例 WBS 正常且随访时间超过 6 个月的患者中,173 例患者在无 TgAb 的情况下,消融后 6-18 个月 TSH-Tg 无法检测,1 例患者 TSH-Tg 检测值为 1.2ng/ml,1 例患者 TgAb 阳性。152 例患者 n-US 正常,3 例患者 n-US 假阳性。平均随访 4 年后,2 例(1%)患者复发,均为侵袭性组织学变异。唯一的复发危险因素是侵袭性组织学变异(P = 0.03)。总之,在消融时 TSH-Tg 无法检测且不存在 TgAb 的情况下,术后 TSH-Tg 无法检测的情况很常见。在这些患者中,消融后 6-18 个月重复检测 TSH-Tg 并无益处。如果不存在 N1 和侵袭性组织学变异,可以避免进行(131)I 消融。

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