甲状腺癌中 CCDC6-RET 和 NCOA4-RET 融合的临床病理特征:一项针对中国人群的单中心回顾性队列研究

IF 5.8 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM Thyroid Pub Date : 2024-10-01 Epub Date: 2024-09-27 DOI:10.1089/thy.2024.0151
Zhiting Wang, Qianlan Yao, Longlong Bao, Heng Chang, Min Ren, Tian Xue, Ran Wei, Chengli Yu, Qian Wang, Yu Wang, Bo Ping, Qianming Bai, Xiaoyan Zhou, Xiaoli Zhu
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Detailed clinicopathological data of thyroid cancer cases with <i>RET</i> fusions were collected. <b><i>Results:</i></b> Among 2300 thyroid cancer cases, <i>RET</i> fusions were exclusively found in PTC or differentiated high-grade thyroid carcinoma (DHGTC) cases (2234 cases), absent in other types (66 cases). Of the 2234 PTC or DHGTC cases, 113 (5.06%) exhibited <i>RET</i> fusions, including 100 primary cases. Coiled-coil domain containing 6 (<i>CCDC6)-RET</i> fusions predominated (78.0%, 78/100), with nuclear receptor coactivator 4 (<i>NCOA4)-RET</i> fusions representing 22.0% (22/100). <i>NCOA4-RET</i> fusions were more prevalent in patients aged 45 years and older (54.5% vs. 28.2%, <i>p =</i> 0.021) and DHGTC cases (<i>p</i> < 0.05) and associated with higher rates of lymph node metastases (90.9% vs. 67.9%, <i>p =</i> 0.032). <i>CCDC6-RET</i> fusion exhibited a higher prevalence of Hashimoto's thyroiditis (HT) (67.9% vs. 22.7%, <i>p</i> < 0.001) and elevated thyroglobulin antibody levels (14.11 [1.86-174.32] IU/mL vs. 2.01 [1.14-15.41] IU/mL, <i>p =</i> 0.018). Moreover, <i>CCDC6-RET</i> fusion predominantly occurred in classical PTC (56.4%, 44/78) and infiltrative follicular PTC (17.9%, 14/78), whereas <i>NCOA4-RET</i> fusion was more frequent in classical PTC (36.4%, 8/22), solid PTC (27.3%, 6/22), and DHGTC (27.3%, 6/22). <i>RET</i> fusions with compound mutations were associated with older age (≥45 years) and bilateral thyroid involvement. Follow-up data showed a higher recurrence rate in the <i>RET</i> fusion group compared with the <i>BRAF<sup>V600E</sup></i> mutation group (5.0% vs. 0.0%, <i>p =</i> 0.018). 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引用次数: 0

摘要

背景:转染过程中的重排(RET)原癌基因融合在甲状腺乳头状癌(PTC)中很常见,不同种族群体的情况各不相同。然而,对 RET 融合类型的全面比较却很有限。本研究旨在确定中国甲状腺癌病例队列中主要的RET融合类型,并分析其临床病理特征:这项单中心回顾性队列研究利用新一代测序技术对福尔马林固定、石蜡包埋的组织样本进行甲状腺癌数据分析。研究收集了RET融合甲状腺癌病例的详细临床病理数据:在2300例甲状腺癌病例中,RET融合只出现在PTC或分化型高级别甲状腺癌(DHGTC)病例(2234例)中,其他类型的甲状腺癌病例(66例)中没有RET融合。在2234例PTC或DHGTC病例中,有113例(5.06%)表现出RET融合,其中包括100例原发性病例。其中以 CCDC6-RET 融合为主(78.0%,78/100),NCOA4-RET 融合占 22.0%(22/100)。NCOA4-RET融合在45岁及以上患者(54.5% vs. 28.2%,P = 0.021)和DHGTC病例(P < 0.05)中更常见,并且与更高的淋巴结转移率相关(90.9% vs. 67.9%,P = 0.032)。CCDC6-RET融合病例的桥本氏甲状腺炎发病率更高(67.9% vs. 22.7%,P < 0.001),甲状腺球蛋白抗体水平升高(14.11 [1.86-174.32] IU/mL vs. 2.01 [1.14-15.41] IU/mL,P = 0.018)。此外,CCDC6-RET融合主要发生在典型的PTC(56.4%,44/78)和浸润性滤泡型PTC(17.9%,14/78),而NCOA4-RET融合更常见于典型的PTC(36.4%,8/22)、实性PTC(27.3%,6/22)和DHGTC(27.3%,6/22)。复合突变的RET融合与年龄较大(≥45岁)和双侧甲状腺受累有关。随访数据显示,与BRAF V600E突变组相比,RET融合组的复发率更高(5.0% vs. 0.0%,P = 0.018)。虽然NCOA4-RET组的复发率在数字上高于CCDC6-RET组(9.1% vs. 3.8%),但差异无统计学意义(P = 0.559):结论:在中国甲状腺癌病例中,RET融合是PTC或DHGTC病例的特异性基因。CCDC6-RET和NCOA4-RET融合表现出不同的临床病理特征,其中NCOA4-RET更具侵袭性。
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Clinicopathological Features of CCDC6-RET and NCOA4-RET Fusions in Thyroid Cancer: A Single-Center Retrospective Cohort Study in a Chinese Population.

Background: The rearranged during transfection (RET) proto-oncogene fusion is common in papillary thyroid cancer (PTC), varying across ethnic groups. However, comprehensive comparisons of RET fusion types are limited. This study aims to identify predominant RET fusions and analyze their clinicopathological characteristics in a cohort of Chinese thyroid cancer cases. Methods: This single-center retrospective cohort study analyzed thyroid cancer data, utilizing next-generation sequencing on formalin-fixed, paraffin-embedded tissue samples. Detailed clinicopathological data of thyroid cancer cases with RET fusions were collected. Results: Among 2300 thyroid cancer cases, RET fusions were exclusively found in PTC or differentiated high-grade thyroid carcinoma (DHGTC) cases (2234 cases), absent in other types (66 cases). Of the 2234 PTC or DHGTC cases, 113 (5.06%) exhibited RET fusions, including 100 primary cases. Coiled-coil domain containing 6 (CCDC6)-RET fusions predominated (78.0%, 78/100), with nuclear receptor coactivator 4 (NCOA4)-RET fusions representing 22.0% (22/100). NCOA4-RET fusions were more prevalent in patients aged 45 years and older (54.5% vs. 28.2%, p = 0.021) and DHGTC cases (p < 0.05) and associated with higher rates of lymph node metastases (90.9% vs. 67.9%, p = 0.032). CCDC6-RET fusion exhibited a higher prevalence of Hashimoto's thyroiditis (HT) (67.9% vs. 22.7%, p < 0.001) and elevated thyroglobulin antibody levels (14.11 [1.86-174.32] IU/mL vs. 2.01 [1.14-15.41] IU/mL, p = 0.018). Moreover, CCDC6-RET fusion predominantly occurred in classical PTC (56.4%, 44/78) and infiltrative follicular PTC (17.9%, 14/78), whereas NCOA4-RET fusion was more frequent in classical PTC (36.4%, 8/22), solid PTC (27.3%, 6/22), and DHGTC (27.3%, 6/22). RET fusions with compound mutations were associated with older age (≥45 years) and bilateral thyroid involvement. Follow-up data showed a higher recurrence rate in the RET fusion group compared with the BRAFV600E mutation group (5.0% vs. 0.0%, p = 0.018). Although the NCOA4-RET group showed a numerically higher recurrence rate compared with CCDC6-RET (9.1% vs. 3.8%), this difference was not statistically significant (p = 0.559). Conclusions: RET fusions are specific to PTC or DHGTC cases among Chinese thyroid cancer cases. CCDC6-RET and NCOA4-RET fusions exhibited distinct clinicopathological features, with NCOA4-RET being more aggressive.

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来源期刊
Thyroid
Thyroid 医学-内分泌学与代谢
CiteScore
12.30
自引率
6.10%
发文量
195
审稿时长
6 months
期刊介绍: This authoritative journal program, including the monthly flagship journal Thyroid, Clinical Thyroidology® (monthly), and VideoEndocrinology™ (quarterly), delivers in-depth coverage on topics from clinical application and primary care, to the latest advances in diagnostic imaging and surgical techniques and technologies, designed to optimize patient care and outcomes. Thyroid is the leading, peer-reviewed resource for original articles, patient-focused reports, and translational research on thyroid cancer and all thyroid related diseases. The Journal delivers the latest findings on topics from primary care to clinical application, and is the exclusive source for the authoritative and updated American Thyroid Association (ATA) Guidelines for Managing Thyroid Disease.
期刊最新文献
Examining Why Thyroid Cancer Incidence Is High in Women. Differential Ultrasound Rates Mirror Sex Disparities in Thyroid Cancer. Irwin Klein, MD (1946-2024). Surgical and Pathological Challenges in Thyroidectomy after Thermal Ablation of Thyroid Nodules. Association Between Environmental Air Pollution and Thyroid Cancer and Nodules: A Systematic Review.
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