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Plasma cell-free DNA levels and integrity in patients with chest radiological findings: NSCLC versus benign lung nodules

机译:胸部影像学检查患者的血浆无细胞DNA水平和完整性:NSCLC与良性肺结节

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摘要

Effective discrimination between lung cancer and benign tumours is a common clinical problem in the differential diagnosis of solitary pulmonary nodules. The analysis of cell-free DNA (cfDNA) in blood may greatly aid the early detection of lung cancer by evaluating cancer-related alterations. The plasma cfDNA levels and integrity were analysed in 65 non-small cell lung cancer (NSCLC) patients, 28 subjects with benign lung tumours, and 16 healthy controls using real-time PCR. The NSCLC patients demonstrated significantly higher mean plasma cfDNA levels compared with those with benign tumours (P = 0.0009) and healthy controls (P < 0.0001). The plasma cfDNA integrity in healthy individuals was significantly different than that found in patients with NSCLC or benign lung tumours (P < 0.0003). In ROC curve analysis, plasma cfDNA levels >2.8 ng/ml provided 86.4% sensitivity and 61.4% specificity in discriminating NSCLC from benign lung pathologies and healthy controls. cfDNA integrity showed better discriminatory power (91% sensitivity, 68.2% specificity). These data demonstrate that plasma cfDNA concentration and integrity analyses can significantly differentiate between NSCLC and benign lung tumours. The diagnostic capacity of the quantitative cfDNA assay is comparable to the values presented by conventional imaging modalities used in clinical practice. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
机译:在孤立性肺结节的鉴别诊断中,有效区分肺癌和良性肿瘤是一个常见的临床问题。血液中无细胞DNA(cfDNA)的分析可通过评估与癌症相关的改变而大大有助于肺癌的早期检测。使用实时PCR分析了65例非小细胞肺癌(NSCLC)患者,28例良性肺肿瘤患者和16例健康对照的血浆cfDNA水平和完整性。与良性肿瘤(P = 0.0009)和健康对照组(P <0.0001)相比,NSCLC患者的血浆cfDNA平均血浆水平显着更高。健康个体的血浆cfDNA完整性与NSCLC或良性肺肿瘤患者的血浆cfDNA完整性显着不同(P <0.0003)。在ROC曲线分析中,血浆cfDNA水平> 2.8 ng / ml可将NSCLC与良性肺部疾病和健康对照区分开来,可提供86.4%的灵敏度和61.4%的特异性。 cfDNA完整性显示出更好的区分能力(灵敏度为91%,特异性为68.2%)。这些数据表明血浆cfDNA浓度和完整性分析可以显着区分NSCLC和良性肺肿瘤。定量cfDNA分析的诊断能力可与临床实践中使用的常规成像方法提供的值相媲美。 (C)2016 Elsevier Ireland Ltd.保留所有权利。

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