Department of Surgical Oncology, The First Affiliated Hospital of Wenzhou Medical College, Wenzhou 325000, China.
World J Surg Oncol. 2013 Mar 5;11:56. doi: 10.1186/1477-7819-11-56.
To confirm whether clinical and biochemical parameters or Hashimoto's thyroiditis (HT) could predict the risks of malignancy among subjects who underwent thyroidectomy, as well as to determine the influence of HT on the biological behavior of papillary thyroid cancer (PTC).
A total of 2,052 patients who underwent initial thyroidectomy were enrolled between June 2006 and August 2008. Serum free T4, free T3, thyrotropin (TSH), thyroglobulin, thyroglobulin antibody, antimicrosomal antibody, tumor-associated status, and thyroid disorders were documented.
Binary logistic regression analysis was performed to define the risk predictors for thyroid cancer. Finally, calcification, HT, TSH, and age, were entered into the multivariate model. Multivariate logistic regression analysis revealed the risk of thyroid cancer increases in parallel with TSH concentration within normal range, and the risk for malignancy significantly increased with serum TSH 1.97-4.94 mIU/L, compared with TSH less than 0.35 mIU/L (OR = 1.951, 95% CI = 1.201-3.171, P = 0.007). Increased risks of thyroid cancer were also detected among the patients with HT (OR = 3.732, 95% CI = 2.563-5.435), and microcalcification (OR = 14.486, 95% CI = 11.374-18.449). The effects of HT on the aggressiveness of PTC were not observed in extrathyroidal invasion (P = 0.347), capsular infiltration (P = 0.345), angioinvasion (P = 0.512), and lymph node metastases (P = 0.634).
The risk of malignancy increases in patients with higher level TSH within normal range, as well as the presence of HT and microcalcification. No evidence suggests that coexistent HT alleviates the aggressiveness of PTC.
为了确定临床和生化参数或桥本甲状腺炎(HT)是否可以预测接受甲状腺切除术的患者发生恶性肿瘤的风险,以及确定 HT 对甲状腺乳头状癌(PTC)的生物学行为的影响。
共纳入 2006 年 6 月至 2008 年 8 月期间接受初次甲状腺切除术的 2052 例患者。记录血清游离 T4、游离 T3、促甲状腺激素(TSH)、甲状腺球蛋白、甲状腺球蛋白抗体、抗微粒体抗体、肿瘤相关状态和甲状腺疾病。
采用二项逻辑回归分析确定甲状腺癌的风险预测因素。最后,将钙化、HT、TSH 和年龄纳入多变量模型。多变量逻辑回归分析显示,随着正常范围内 TSH 浓度的增加,甲状腺癌的风险平行增加,与 TSH 小于 0.35 mIU/L 相比,TSH 在 1.97-4.94 mIU/L 范围内,恶性肿瘤的风险显著增加(OR = 1.951,95%CI = 1.201-3.171,P = 0.007)。HT(OR = 3.732,95%CI = 2.563-5.435)和微钙化(OR = 14.486,95%CI = 11.374-18.449)患者甲状腺癌的风险也增加。未发现 HT 对 PTC 侵袭性的影响在甲状腺外侵犯(P = 0.347)、包膜浸润(P = 0.345)、血管侵犯(P = 0.512)和淋巴结转移(P = 0.634)中存在差异。
在正常范围内 TSH 水平较高的患者中,以及存在 HT 和微钙化的患者中,恶性肿瘤的风险增加。没有证据表明共存的 HT 会减轻 PTC 的侵袭性。