Chen Xiang-Yi, Tan Yang, Wang Dawei, Wei Zhi-Xiao
Department of Nuclear Medicine, The First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
Department of Pathology, The First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
Br J Radiol. 2024 Aug 1;97(1160):1423-1430. doi: 10.1093/bjr/tqae118.
To investigate the clinical character of differentiated thyroid cancer (DTC) coexisting with Hashimoto's thyroiditis (HT) and provide state-of-art evidence for personalized radioactive iodine-131 therapy (RAIT) for patients coexisting with HT.
From January 2000 to January 2023, PubMed, Embase, and Web of Science databases were searched for relevant original articles that published in English on the RAIT efficacy for DTC with HT. RevMan 5.4 and Stata 17.0 were used for data analysis.
Eleven studies involving 16 605 DTC patients (3321 with HT) were included. HT was more frequent in female (OR: 2.90, 95% confidence interval [CI]: 1.77-4.76, P < .00001). The size of tumour (MD: -0.20, 95% CI: -0.30 to -0.11), extrathyroidal extension rate (OR: 0.77, 95% CI: 0.67-0.90), and metastasis rate (OR: 0.18, 95% CI: 0.08-0.41) were less in HT, but tumour, node, metastasis (TNM) stage had no significant difference among HT and non-HT group. Disease-free survival (DFS) rate (OR: 1.96, 95% CI: 1.57-2.44, P < .00001), 5-year DFS (OR: 1.73, 95% CI: 1.04-2.89, P = .04), and 10-year DFS (OR: 1.56, 95% CI: 1.17-2.09, P = .003) were higher in HT group. The recurrent (OR: 0.62, 95% CI: 0.45-0.83, P = .002), RAIT dosage (MD = -38.71, 95% CI: -60.86 to -16.56, P = .0006), and treatment (MD: -0.13, 95% CI: -0.22 to -0.03, P = .008) were less in HT group.
DTC coexisting with HT was associated with less invasion. DFS of HT group was higher than non-HT group after RAIT. Low-dose treatment did not impair the efficacy of RAIT in DTC with HT.
Hashimoto's thyroiditis is a risk for DTC, but it minimalizes the progression of cancer and enhance the efficacy of RAIT, which should be considered in personalizing RAIT.
探讨分化型甲状腺癌(DTC)合并桥本甲状腺炎(HT)的临床特征,为HT合并DTC患者的个体化放射性碘-131治疗(RAIT)提供最新证据。
检索2000年1月至2023年1月期间在PubMed、Embase和Web of Science数据库中发表的关于HT合并DTC的RAIT疗效的英文相关原创文章。使用RevMan 5.4和Stata 17.0进行数据分析。
纳入11项研究,共16605例DTC患者(其中3321例合并HT)。HT在女性中更为常见(比值比:2.90,95%置信区间[CI]:1.77 - 4.76,P <.00001)。HT患者的肿瘤大小(平均差:-0.20,95% CI:-0.30至-0.11)、甲状腺外侵犯率(比值比:0.77,95% CI:0.67 - 0.90)和转移率(比值比:0.18,95% CI:0.08 - 0.41)较低,但肿瘤、淋巴结、转移(TNM)分期在HT组和非HT组之间无显著差异。HT组的无病生存率(DFS)(比值比:1.96,95% CI:1.57 - 2.44,P <.00001)、5年DFS(比值比:1.73,95% CI:1.04 - 2.89,P = 0.04)和10年DFS(比值比:1.56,95% CI:1.17 - 2.09,P = 0.003)较高。HT组的复发率(比值比:0.62,95% CI:0.45 - 0.83,P = 0.002)、RAIT剂量(平均差 = -38.71,95% CI:-60.86至-16.56,P = 0.0006)和治疗次数(平均差:-0.13,95% CI:-0.22至-0.03,P = 0.008)较少。
DTC合并HT与侵袭性较低有关。RAIT治疗后HT组的DFS高于非HT组。低剂量治疗不会损害HT合并DTC的RAIT疗效。
桥本甲状腺炎是DTC的一个危险因素,但它可使癌症进展最小化并提高RAIT的疗效,在RAIT个体化时应予以考虑。