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Expression of Circulating Microparticles for the Diagnosis of Non-small Cell Lung Cancer: Clinicopathological Correlations and Prognostic Value

机译:循环微粒对非小细胞肺癌诊断的表达:临床病理相关性和预后价值

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Increased values of circulating microparticles (MPs) have been reported in solid tumors including non-small cell lung cancer (NSCLC). We therefore investigated the utility of baseline MPs in the clinical setting of patients with NSCLC. Quantification of MPs in the plasma was performed by flowcytometry. Baseline MP values were correlated with clinical patients' characteristics, estimated tumor volume (ETV) and treatment response. Receiver operating characteristics (ROC) curves were plotted to discriminate between patients and controls in order to determine the diagnostic value of circulating MPs in NSCLC. Our prospective study included 134 NSCLC patients (98 at initial diagnosis, ID and 36 at relapse, R) and 30 healthy individuals. The mean of baseline MP numbers was significantly higher in patients presented either at ID or R than in controls (p<0.0001). Basal MP numbers were inversely correlated with ETV values (p=0.04). In addition, the difference in MP levels at diagnosis was significant according to tumor histology (p=0.02) and primary tumor size (p=0.0007). Using ROC analysis, the optimal cutoff value for baseline MPs was 1307 events/μL with a sensitivity and a specificity of 67.3% and 90.0%, respectively. High MPs expression was significantly associated with low-level smoking degree (p=0.001), non-squamous cell types (p=0.017) and decreased tumor size (p=0.003). Our results suggest that high baseline MP values could be an indicator of tumor growth inhibition in NSSLC. Furthermore, high expression of circulating MPs at diagnosis might predict good prognosis in NSCLC patients.
机译:在包括非小细胞肺癌(NSCLC)的固体肿瘤中报道了循环微粒(MPS)的增加。因此,我们研究了基线MPS在NSCLC患者的临床环境中的效用。通过流式细胞术进行等离子体中MP的定量。基线MP值与临床患者的特征相关,估计肿瘤体积(ETV)和治疗反应。接收器操作特性(ROC)曲线被绘制以区分患者和对照,以确定NSCLC中循环MPS的诊断值。我们的前瞻性研究包括134名NSCLC患者(98名初期诊断,ID和复发,R)和30名健康个体。在id或r的患者患者中,基线MP编号的平均值明显高于对照(P <0.0001)。基础MP编号与ETV值与eDV值相相关(P = 0.04)。此外,根据肿瘤组织学(P = 0.02)和原发性肿瘤大小(p = 0.0007),MP水平的差异很大。使用ROC分析,基线MPS的最佳截止值分别为1307次活动/μL,敏感性分别为67.3%和90.0%。高MPS表达与低水平吸烟度(P = 0.001),非鳞状细胞类型(P = 0.017)和肿瘤大小降低(P = 0.003)显着相关。我们的结果表明,高基线MP值可能是NSSLC中肿瘤生长抑制的指标。此外,在诊断中循环MPS的高表达可能预测NSCLC患者的良好预后。

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