Endocrine Oncology Unit, Department of Endocrine and Metabolic Diseases, IRCCS Istituto Auxologico Italiano, Milan, Italy.
Department of Statistical Sciences and Sapienza University of Rome, Rome, Italy.
Thyroid. 2023 Nov;33(11):1318-1326. doi: 10.1089/thy.2023.0052. Epub 2023 Oct 19.
There is some controversy on the potential relationship between autoimmune processes and clinicopathologic features as well as prognosis of differentiated thyroid cancer (DTC), and the evidence is limited by its largely retrospective nature. We examined the relationship between the presence of autoimmune thyroiditis (AT) and 1-year thyroid cancer treatment outcomes in a large multicenter study using prospectively collected data. We included data from consecutive DTC patients enrolled in the Italian Thyroid Cancer Observatory (ITCO) database (NCT04031339). We divided the groups according to the presence (AT) or absence (no autoimmune thyroiditis [noAT]) of associated AT. We used propensity score matching to compare the clinical features and outcomes between the two groups at 1-year follow-up. We included data from 4233 DTC patients, including 3172 (75%) females. The American Thyroid Association (ATA) risk levels were as follows: 51% (2160/4233) low risk, 41.3% (1750/4233) intermediate risk, and 7.6% (323/4233) high risk. There were 1552 patients (36.7%) who had AT. Before propensity score matching, AT patients were significantly younger and had a smaller and bilateral tumor ( < 0.0001). Patients with AT more frequently fell into the low- and intermediate-risk categories, while the ATA high risk was more frequent among noAT patients ( = 0.004). After propensity score matching, patients with AT more frequently showed evidence of disease (structural/biochemical incomplete response) versus excellent/indeterminate response, compared with patients without AT (7.3% vs. 4.5%, = 0.001), with an odds ratio of 1.86 ([confidence interval: 1.3-2.6], = 0.0001). However, when considering only structural persistence as the outcome, no statistically significant differences were observed between patients with or without AT (3.4% vs. 2.7%, = 0.35). The elevated risk associated with the ATA intermediate and high risk at diagnosis remained consistently statistically significant. In this large prospective series, biochemical persistence was more frequent, at 1-year follow-up, in AT patients. However, there was no significant association between the presence of AT and structural persistence of disease. These findings may be explained by the presence of a residual thyroid tissue.
在自身免疫过程与分化型甲状腺癌(DTC)的临床病理特征和预后之间存在一些争议,而且由于其主要是回顾性研究,证据有限。我们使用前瞻性收集的数据,在一项大型多中心研究中检查了自身免疫性甲状腺炎(AT)的存在与 1 年内甲状腺癌治疗结果之间的关系。我们纳入了意大利甲状腺癌观察站(ITCO)数据库(NCT04031339)连续入组的 DTC 患者的数据。我们根据是否存在相关的 AT(AT)或不存在(无自身免疫性甲状腺炎[无 AT])将两组分组。我们使用倾向评分匹配比较两组在 1 年随访时的临床特征和结局。我们纳入了 4233 例 DTC 患者的数据,包括 3172 例(75%)女性。美国甲状腺协会(ATA)风险水平如下:51%(2160/4233)低风险,41.3%(1750/4233)中风险和 7.6%(323/4233)高风险。有 1552 例患者(36.7%)患有 AT。在进行倾向评分匹配之前,AT 患者明显更年轻,肿瘤更小且为双侧(<0.0001)。AT 患者更常归入低风险和中风险类别,而无 AT 患者更常归入 ATA 高风险类别(=0.004)。进行倾向评分匹配后,与无 AT 患者相比,AT 患者更常出现疾病证据(结构/生化不完全缓解)而不是完全缓解/不确定缓解(7.3%比 4.5%,=0.001),比值比为 1.86(95%置信区间:1.3-2.6],=0.0001)。但是,当仅考虑结构持续存在作为结局时,有或无 AT 的患者之间未观察到统计学上的显著差异(3.4%比 2.7%,=0.35)。诊断时 ATA 中危和高危与风险升高之间的关联仍然具有统计学意义。在这项大型前瞻性研究中,AT 患者在 1 年随访时生化持续存在的频率更高。然而,AT 的存在与疾病的结构持续存在之间没有显著关联。这些发现可以用残留甲状腺组织的存在来解释。