Department of Pathology and Laboratory Medicine, David Geffen School of Medicine at UCLA, California, Los Angeles, USA.
Diagn Cytopathol. 2024 Nov;52(11):627-632. doi: 10.1002/dc.25373. Epub 2024 Jun 15.
The increased usage and adaptation of molecular testing of thyroid fine needle aspirations (FNA) has expanded the variety and number of gene fusions identified. While the identified number of molecular alterations is increasing, the definitive association between preoperative molecular analysis and phenotype has yet to be established. The aim of this study was to examine Thyroid adenoma-associated (THADA)-IGF2BP3 molecular fusions with FNA categorization, surgical pathology diagnosis, and other molecular alterations detected by ThyroSeq Genomic Classifier testing.
FNA cytology samples of thyroid nodules from 04/2017 to 01/2023 with the diagnosis of atypia of undetermined significance or follicular lesion of undetermined significance (AUS/FLUS; Bethesda III) or follicular neoplasm suspicious for follicular neoplasm (FN/SFN; Bethesda IV) with associated ThyroSeqV3 testing were reviewed. Parameters including patient demographics, FNA diagnosis, ThyroSeq V3 results, and surgical pathology follow up were examined.
87 out of 249 (35%) FNA specimens of thyroid nodules displayed molecular alterations. 64 cases (74%) had a cytology diagnosis of AUS and 23 (26%) had FN. RAS mutation was observed in 48 cases. On surgical follow-up, 17 (35%) cases showed non-invasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTP), while 14 (29%) patients had a malignant diagnosis. THADA-IGF2BP3 fusions were seen in 8 cases, all with NIFTP on surgical pathology follow-up (100%).
Analysis of THADA-IGF2BP3 fusion, in our institutional series, shows close association with NIFTP cases. THADA-IGF2BP3 fusion, which seems to be a favorable prognostic indicator in general, may serve as a molecular marker for non-invasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTP).
甲状腺细针抽吸物(FNA)的分子检测使用增加和适应,扩大了鉴定出的基因融合的种类和数量。虽然鉴定出的分子改变数量在增加,但术前分子分析与表型之间的明确关联尚未建立。本研究的目的是检查甲状腺腺瘤相关(THADA)-IGF2BP3 分子融合与 FNA 分类、手术病理诊断以及通过 ThyroSeq 基因组分类器检测到的其他分子改变之间的关系。
回顾 2017 年 4 月至 2023 年 1 月期间具有不明确意义的非典型性或滤泡性病变(AUS/FLUS;Bethesda III)或滤泡性肿瘤疑似滤泡性肿瘤(FN/SFN;Bethesda IV)的甲状腺结节的 FNA 细胞学样本,并进行 ThyroSeqV3 检测。检查的参数包括患者人口统计学、FNA 诊断、ThyroSeq V3 结果和手术病理随访。
87 例甲状腺结节的 FNA 标本中有 87 例(35%)显示分子改变。64 例(74%)的细胞学诊断为 AUS,23 例(26%)为 FN。48 例有 RAS 突变。在手术随访中,17 例(35%)病例显示非浸润性滤泡性甲状腺肿瘤伴乳头状核特征(NIFTP),14 例(29%)患者有恶性诊断。在我们的机构系列中,观察到 8 例 THADA-IGF2BP3 融合,所有病例在手术病理随访中均为 NIFTP(100%)。
在我们的机构系列中,分析 THADA-IGF2BP3 融合与 NIFTP 病例密切相关。THADA-IGF2BP3 融合似乎是一种普遍有利的预后指标,可作为具有乳头状核特征的非浸润性滤泡性甲状腺肿瘤(NIFTP)的分子标志物。