Toubeau Michel, Touzery Claude, Arveux Patrick, Chaplain Gilles, Vaillant Geneviève, Berriolo Alina, Riedinger Jean-Marc, Boichot Christophe, Cochet Alexandre, Brunotte François
Department of Nuclear Medicine, Centre Georges François Leclerc, Dijon, France.
J Nucl Med. 2004 Jun;45(6):988-94.
The aim of our study was to evaluate and compare in thyroid cancer patients the predictive value for disease progression of thyroglobulin (Tg) levels measured under thyroid-stimulating hormone (TSH) stimulation, in the postoperative period just before (131)I ablative therapy and at the time of control 6-12 mo later.
Two-hundred twelve consecutive patients treated for a well-differentiated thyroid carcinoma (184 papillary, 28 follicular) with no initial distant metastases were retrospectively studied. All patients had a total or near-total thyroidectomy followed by ablation with 3.7 GBq (131)I. Tg levels were determined just before ablative therapy (Tg1) and 6-12 mo later (Tg2). Thresholds of 30 and 10 ng/mL were used for Tg1 and Tg2, respectively. Univariate and multivariate analyses were performed to assess the predictive value for disease progression of the 2 Tg determinations.
Thirty patients had a Tg1 level > 30 ng/mL. Six to 12 mo later, 30 patients had a Tg2 level > 10 ng/mL, 19 of whom had initially a Tg1 level > 30 ng/mL. Disease progression was reported in 20 patients (9%). Progression-free survival rates were significantly lower in patients with a low Tg1 or Tg2 level but the difference was more important with Tg2. With univariate analysis, 5 variables were significantly associated with disease progression: Tg2, Tg1, node invasion, extrathyroidal extension, and tumor size. With multivariate analysis, only Tg2 (odds ratio [OR] = 16.4; 95% confidence interval [95% CI] = 5.7-47.4; P < 0.001) and node invasion (OR = 2.7; 95% CI = 1.0-7.2; P = 0.04) had an independent prognostic value. When only initial parameters were considered, Tg1 and node invasion were the 2 independent prognostic factors. The OR decreased for Tg1 (OR = 10.1; 95% CI = 4.0-25.7; P < 0.001) but increased for node invasion (OR = 4.4; 95% CI = 1.7-11.2; P = 0.002).
Among all clinical and tumoral variables, lymph node invasion and serum Tg level are 2 important parameters to define the risk of disease progression. Although Tg2 appears more significant than Tg1, both Tg levels measured under TSH stimulation, in the postoperative period and a few months after ablative therapy, have a predictive value. In clinical practice, patients at risk can be selected as soon as the initial lymph node status and Tg1 level are known.
本研究的目的是评估并比较甲状腺癌患者在促甲状腺激素(TSH)刺激下,术后(131)I消融治疗前及6 - 12个月后复查时所测甲状腺球蛋白(Tg)水平对疾病进展的预测价值。
回顾性研究212例连续接受治疗的分化型甲状腺癌患者(184例乳头状癌,28例滤泡状癌),这些患者均无远处转移。所有患者均接受了甲状腺全切或近全切术,随后给予3.7 GBq(131)I进行消融治疗。分别在消融治疗前(Tg1)和6 - 12个月后(Tg2)测定Tg水平。Tg1和Tg2的阈值分别设定为30 ng/mL和10 ng/mL。进行单因素和多因素分析以评估这两个Tg测定值对疾病进展的预测价值。
30例患者的Tg1水平>30 ng/mL。6 - 12个月后,30例患者的Tg2水平>10 ng/mL,其中19例患者最初的Tg1水平>30 ng/mL。报告有20例患者(9%)出现疾病进展。Tg1或Tg2水平低的患者无进展生存率显著较低,但Tg2的差异更为明显。单因素分析显示,5个变量与疾病进展显著相关:Tg2、Tg1、淋巴结侵犯、甲状腺外侵犯和肿瘤大小。多因素分析显示,只有Tg2(比值比[OR]=16.4;95%置信区间[95%CI]=5.7 - 47.4;P<0.001)和淋巴结侵犯(OR = 2.7;95%CI = 1.0 - 7.2;P = 0.04)具有独立的预后价值。仅考虑初始参数时,Tg1和淋巴结侵犯是两个独立的预后因素。Tg1的OR值降低(OR = 10.1;95%CI = 4.0 - 25.7;P<0.001),而淋巴结侵犯的OR值升高(OR = 4.4;95%CI = 1.7 - 11.2;P = 0.002)。
在所有临床和肿瘤变量中,淋巴结侵犯和血清Tg水平是定义疾病进展风险的两个重要参数。尽管Tg2似乎比Tg1更具显著性,但在术后及消融治疗后几个月在TSH刺激下所测的两个Tg水平均具有预测价值。在临床实践中,一旦知道初始淋巴结状态和Tg1水平,就可以筛选出有风险的患者。