Suspicious ultrasound and clinicopathological features of papillary thyroid carcinoma predict the status of TERT promoter

被引:10
|
作者
Shi, Hui [1 ,2 ,3 ]
Guo, Le-Hang [1 ,2 ,3 ]
Zhang, Yi-Feng [1 ,2 ,3 ]
Fu, Hui-Jun [2 ,3 ,4 ]
Zheng, Jia-Yi [2 ,3 ,4 ]
Wang, Han-Xiang [1 ,2 ,3 ]
Zhao, Chong-Ke [1 ,2 ,3 ]
Xu, Hui-Xiong [1 ,2 ,3 ]
机构
[1] Tongji Univ, Sch Med, Shanghai Peoples Hosp 10, Dept Med Ultrasound,Canc Ctr,Ultrasound Res & Edu, Shanghai 200072, Peoples R China
[2] Tongji Univ, Sch Med, Thyroid Inst, Shanghai 200072, Peoples R China
[3] Shanghai Ctr Thyroid Dis, Shanghai 200072, Peoples R China
[4] Tongji Univ, Sch Med, Shanghai Peoples Hosp 10, Dept Pathol, Shanghai 200072, Peoples R China
基金
中国国家自然科学基金;
关键词
Ultrasound; Clinicopathological; Prediction; TERT promoter; Papillary thyroid cancer; MAJOR INDICATOR; MUTATIONS; CANCER; ASSOCIATION; BRAF; RECURRENCE; NODULES; BRAF(V600E); TELOMERASE; MANAGEMENT;
D O I
10.1007/s12020-020-02214-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose To investigate the value of ultrasound (US) and clinicopathological features of papillary thyroid cancer (PTC) in predicting Telomerase Reverse Transcriptase (TERT) promoter mutations. Methods Preoperative US images of 351 surgically confirmed PTCs were evaluated in terms of PTCs size and US features. The basic clinicopathological features were also retrieved. Univariate and multivariate analyses were performed to identify the risk factors for TERT promoter mutations. A scoring system was developed based on the cumulative number of risk factors. The area under the receiver operating characteristic curve (AUC) and cut-off value were calculated to evaluate the diagnostic performance of the scoring system for predicting TERT promoter mutations. Results TERT promoter mutations were found in 4.84% (17/351) of patients with PTCs. Patient age >50 years (OR: 6.244, P = 0.006), multifocality (OR: 21.071, P = 0.022), taller-than-wide shape (OR: 4.934, P = 0.029), microlobulated margin (OR: 4786, P = 0.032), and capsule contact or involvement (OR: 4.668, P = 0.030) were independent risk factors for TERT promoter mutations. TERT promoter mutations were relevant to more suspicious US and clinicopathological features than TERT promoter wild-type PTC (median, 4 vs. 1, P < 0.001). The cut-off value was 2.5 and the associated AUC was 0.908 (P < 0.001). Conclusions The probability of TERT promoter mutations increases along with the suspicious US features and clinicopathological characteristics, which may help to recognize patients who deserve a different approach, in terms of management and follow-up, in view of the worst outcome associated to this mutation.
引用
收藏
页码:349 / 357
页数:9
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