Division of Endocrinology and Metabolism, Pittsburgh, Pennsylvania, USA.
Division of Endocrine Surgery, Pittsburgh, Pennsylvania, USA.
Thyroid. 2022 Nov;32(11):1346-1352. doi: 10.1089/thy.2022.0337. Epub 2022 Aug 25.
Noninvasive encapsulated follicular variant papillary thyroid carcinoma (EFVPTC) was reclassified as "noninvasive follicular thyroid neoplasm with papillary-like nuclear features" (NIFTP) in 2016. Most existing studies that examined outcomes included patients managed as EFVPTC and only retrospectively reclassified as NIFTP. This is the first study to evaluate the clinicopathologic, molecular, and surveillance characteristics of patients diagnosed with NIFTP at the time of surgery and managed based on this diagnosis. We performed a retrospective cohort study of consecutive cases diagnosed as NIFTP from June 2016 to October 2021 identified from electronic medical records at a large tertiary care institution. Patients with coexisting low-risk thyroid cancers ≥1.0 cm in size or any size aggressive histology were excluded, and review of demographic, clinical, imaging, cytologic, and molecular genetic data was performed. Initial care was delivered according to existing clinical guidelines, with a consensus institutional plan for five-year follow-up after surgery. Among 79 patients with 84 nodules diagnosed as NIFTP after surgery, 83.5% (66/79) were women and the mean age was 51 years (range, 21-84). Mean NIFTP size was 2.4 cm (range 0.15-8.0). On ultrasound, the majority of nodules were categorized as thyroid imaging, reporting and data system TI-RADS 3 (55.3%, 42/76), and TI-RADS 4 (36.8%, 28/76). On cytology, they were typically diagnosed as Bethesda III (69.1%, 47/68) or Bethesda IV (23.5%, 16/68). Molecular testing was performed on 62 nodules, and molecular alterations were found in 93.5% (58/62). The most common alterations identified in NIFTP were mutation (75.4%, 43/57), fusion (12.3%, 7/57), and mutation (7.0%, 4/57). Fifty-two (65.8%) patients underwent lobectomy and 27 (34.2%) total thyroidectomy, and no patient received completion thyroidectomy. Twenty-one patients (26.5%) had coexisting papillary or follicular microcarcinoma. None of the patients received radioiodine ablation. On a mean follow-up of 28.5 months (range, 6-69 months), no structural or biochemical recurrences were observed. In this large cohort of patients with NIFTP diagnosed at the time of surgery and managed typically by lobectomy with no radioiodine ablation, no evidence of tumor recurrence was identified on a limited follow-up. This finding supports indolent clinical course of NIFTP.
2016 年,非侵袭性包裹滤泡型甲状腺癌(EFVPTC)被重新分类为“具有滤泡状肿瘤特征的非侵袭性甲状腺滤泡性肿瘤”(NIFTP)。大多数现有的研究均纳入了接受 EFVPTC 治疗并仅回顾性重新分类为 NIFTP 的患者。这是第一项评估在手术时诊断为 NIFTP 并根据该诊断进行管理的患者的临床病理、分子和监测特征的研究。我们对一家大型三级医疗机构的电子病历中 2016 年 6 月至 2021 年 10 月期间连续诊断为 NIFTP 的病例进行了回顾性队列研究。排除了同时存在≥1.0cm 大小的低风险甲状腺癌或任何大小侵袭性组织学的患者,并对人口统计学、临床、影像学、细胞学和分子遗传学数据进行了回顾。根据现有的临床指南进行初始治疗,并制定了术后五年随访的机构共识计划。在 84 个结节中有 79 个术后诊断为 NIFTP 的患者中,83.5%(66/79)为女性,平均年龄为 51 岁(范围,21-84 岁)。NIFTP 的平均大小为 2.4cm(范围 0.15-8.0cm)。在超声检查中,大多数结节被归类为甲状腺成像报告和数据系统 TI-RADS 3(55.3%,42/76)和 TI-RADS 4(36.8%,28/76)。在细胞学检查中,它们通常被诊断为贝塞斯达 III 级(69.1%,47/68)或贝塞斯达 IV 级(23.5%,16/68)。对 62 个结节进行了分子检测,发现 93.5%(58/62)存在分子改变。在 NIFTP 中最常见的改变是 突变(75.4%,43/57)、 融合(12.3%,7/57)和 突变(7.0%,4/57)。52 名(65.8%)患者接受了 lobectomy,27 名(34.2%)患者接受了全甲状腺切除术,没有患者接受了 completion thyroidectomy。21 名(26.5%)患者同时患有乳头状或滤泡状微癌。没有患者接受放射性碘消融治疗。在平均 28.5 个月(范围 6-69 个月)的随访中,未观察到结构或生化复发。在这项大型 NIFTP 患者队列研究中,患者在手术时即被诊断为 NIFTP,并通常接受 lobectomy 治疗而不进行放射性碘消融治疗,在有限的随访中未发现肿瘤复发的证据。这一发现支持 NIFTP 具有惰性的临床病程。