首页> 美国卫生研究院文献>Frontiers in Oncology >Limited Utility of Circulating Cell-Free DNA Integrity as a Diagnostic Tool for Differentiating Between Malignant and Benign Thyroid Nodules With Indeterminate Cytology (Bethesda Category III)
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Limited Utility of Circulating Cell-Free DNA Integrity as a Diagnostic Tool for Differentiating Between Malignant and Benign Thyroid Nodules With Indeterminate Cytology (Bethesda Category III)

机译:有限的循环无细胞DNA完整性实用程序,作为区分不确定细胞学的恶性甲状腺结节和良性甲状腺结节的诊断工具(贝塞斯达III类)

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摘要

Background: Analysis of plasma circulating cell-free DNA integrity (cfDI) has emerged as a promising tool in the diagnosis of malignant vs. benign tumors. There is limited data on the role of cfDI in thyroid cancer. The goal of this study was to analyze cfDI as a biomarker of malignancy in patients with cytologically indeterminate thyroid nodules.Methods: The cfDI was measured in the plasma of patients with cytologically indeterminate thyroid nodules. All patients underwent plasma collection within 24–72 h before surgical treatment for thyroid nodules. Additionally, samples were collected from seven patients via the vein draining the thyroid and peripheral vein during surgery. Quantitative real-time PCR was performed on the isolated cell-free DNA using two different primer sets (115 and 247 bp) to amplify consensus ALU sequences. The cfDI was calculated as the ratio of ALU247 to ALU115.Results: All data are given as median [25th−75th percentile]. The study group consisted of 67 patients with 100 nodules, 80.6% (54/67) women, aged 43 [33-60] years. There was no difference in cfDI between 29 patients with benign nodules (0.49 [0.41–0.59]) and 38 patients with malignant lesions (0.45 [0.36–0.57], p = 0.19). There was no difference in cfDI in the vein draining the thyroid (0.47 [0.24–1.05]) and peripheral vein (0.48 [0.36–0.56], p = 0.44). In comparison to thyroid cancer patients, patients with benign nodules were characterized by significantly higher concentrations of ALU115 (1,064 [529–2,960] vs. 411 [27–1,049] ng/ml; p = 0.002) and ALU247 (548 [276–1,894] vs. 170 [17-540] ng/ml; p = 0.0005), most likely because benign tumors were larger (3, [1.8–4.1 cm]) than malignant lesions (0.7 [0.23–1.45], p < 0.0001). Women had significantly lower cfDI (0.45 [0.27–0.54]) than men (0.56 [0.44–0.8], p = 0.011).Conclusion: The cfDI measured in the vein draining the thyroid is similar to the cfDI measured in the antecubital vein, validating cfDI measurements by peripheral liquid biopsy. Analysis of cfDI needs to be stratified by patients gender. In contrast to its diagnostic utility in aggressive cancers, cfDI has limited utility as a biomarker of malignancy in cytologically indeterminate thyroid nodules.
机译:背景:分析血浆循环无细胞DNA完整性(cfDI)已成为诊断恶性肿瘤与良性肿瘤的有前途的工具。关于cfDI在甲状腺癌中的作用的数据有限。这项研究的目的是分析cfDI作为细胞学上不确定的甲状腺结节患者恶性肿瘤的生物标志物。方法:在细胞学上不确定的甲状腺结节患者的血浆中测量cfDI。所有患者在接受甲状腺结节手术治疗前的24-72小时内均接受血浆采集。另外,在手术过程中通过排空甲状腺和外周静脉的静脉从七名患者中收集了样本。使用两个不同的引物组(115和247 bp)对分离的无细胞DNA进行定量实时PCR,以扩增共有的ALU序列。 cfDI以ALU247与ALU115的比率计算。结果:所有数据均以中位数[25-75%]给出。该研究组由67例100个结节的患者组成,其中80.6%(54/67)妇女年龄为43 [33-60]岁。 cfDI在29例良性结节(0.49 [0.41-0.59])和38例恶性病变(0.45 [0.36-0.57],p = 0.19)之间没有差异。甲状腺引流静脉(0.47 [0.24-1.05])和周围静脉引流(0.48 [0.36-0.56],p = 0.44)的cfDI没有差异。与甲状腺癌患者相比,良性结节患者的特征是ALU115(1,064 [529–2,960]]和411 [27–1,049] ng / ml; p = 0.002)和ALU247(548 [276–1,894] ] vs. 170 [17-540] ng / ml; p = 0.0005),最可能的原因是良性肿瘤比恶性病变更大(3 [1.8-4.1 cm])(0.7 [0.23-1.45],p <0.0001) 。女性的cfDI(0.45 [0.27–0.54])明显低于男性(0.56 [0.44–0.8],p = 0.011)。结论:在引流甲状腺的静脉中测得的cfDI类似于cfDI在肘前静脉中测量,通过外周液体活检验证cfDI测量。 cfDI的分析需要按患者性别进行分层。与它在侵袭性癌症中的诊断作用相反,cfDI在细胞学上不确定的甲状腺结节中作为恶性生物标志物的作用有限。

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