Safety and Feasibility of US-guided Microwave Ablation for the Treatment of Bethesda III Thyroid Nodules with Negative Eight-Gene Panel Mutational Profile.

IF 5.6 Q1 ONCOLOGY Radiology. Imaging cancer Pub Date : 2025-01-01 DOI:10.1148/rycan.240058
Qingqing Tang, Jiawei Chen, Dengke Zhang, Qingnan Huang, Yong Chen, Xuexin Liang, Kai Zeng, Yuxian Guo, Mingliang Huang, Yanghui Wei
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Abstract

Purpose To evaluate the safety and efficacy of US-guided thermal ablation in the treatment of Bethesda III thyroid nodules with negative eight-gene panel testing results. Materials and Methods This retrospective single-center study included patients with thyroid nodules diagnosed as Bethesda category III (atypia of undetermined significance) at fine-needle aspiration biopsy and with negative eight-gene testing results who were treated with US-guided microwave ablation (MWA) between July 2020 and September 2023. Incidence of complications, technical success rate (TSR), volume reduction rate (VRR), nodule recurrence, and thyroid function were evaluated over a follow-up period of 2 years. Data before and after MWA were compared using variance analysis and the Cochran-Mantel-Haenszel χ2 test. Results A total of 101 Bethesda III nodules were detected in 95 patients (mean ± SD age, 47.08 years ±14.63; 79 female patients, 16 male patients), all of which were completely ablated (100% TSR). Two patients experienced mild neck swelling and pressure sensation after the minimally invasive operation, and the incidence of postoperative complications was 2% (two of 95). None of the patients experienced tumor recurrence or progression. At 2-year follow-up, the mean VRR of the ablated area was 90.88% ± 13.59 in 15 patients; 87% (13 of 15) of these patients had a 100% VRR. There was no evidence of a difference in thyroid function before and after MWA from 1 to 24 months (P = .15-.99). Conclusion US-guided MWA was safe and effective for the treatment of Bethesda III thyroid nodules with negative eight-gene panel testing results. Keywords: Ablation Techniques, Radiation Therapy/Oncology, Head/Neck, Thyroid, Safety, Observer Performance Published under a CC BY 4.0 license.

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目的 评价 US 引导下热消融治疗八基因检测结果为阴性的 Bethesda III 甲状腺结节的安全性和有效性。材料与方法 这项回顾性单中心研究纳入了在细针穿刺活检中被诊断为 Bethesda III 类(意义未定的不典型性)甲状腺结节且八基因检测结果为阴性的患者,这些患者在 2020 年 7 月至 2023 年 9 月期间接受了 US 引导下的微波消融术(MWA)治疗。随访两年,评估并发症发生率、技术成功率(TSR)、体积缩小率(VRR)、结节复发率和甲状腺功能。采用方差分析和 Cochran-Mantel-Haenszel χ2检验比较MWA前后的数据。结果 95 名患者共发现 101 个 Bethesda III 结节(平均 ± SD 年龄,47.08 岁 ± 14.63;79 名女性患者,16 名男性患者),所有结节均被完全消融(100% TSR)。两名患者在微创手术后出现轻度颈部肿胀和压迫感,术后并发症发生率为 2%(95 人中有 2 人)。没有一名患者出现肿瘤复发或恶化。在 2 年的随访中,15 名患者消融区域的平均 VRR 为 90.88% ± 13.59;其中 87% 的患者(15 人中有 13 人)的 VRR 为 100%。从 1 个月到 24 个月,没有证据表明 MWA 前后的甲状腺功能存在差异(P = .15-.99)。结论 US引导下的MWA治疗八基因检测结果为阴性的贝塞斯达III甲状腺结节是安全有效的。关键词消融技术 放射治疗/肿瘤学 头颈部 甲状腺 安全性 观察者表现 以 CC BY 4.0 许可发布。
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