首页> 外文期刊>The Quarterly Journal of Nuclear Medicine >Tissue polypeptide specific antigen (tps) and cytokeratin 19 fragment (CYFRA 21.1) immunoradiometric assay in non small cell lung cancer evaluation
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Tissue polypeptide specific antigen (tps) and cytokeratin 19 fragment (CYFRA 21.1) immunoradiometric assay in non small cell lung cancer evaluation

机译:非小细胞肺癌组织多肽特异性抗原(tps)和细胞角蛋白19片段(CYFRA 21.1)免疫放射分析

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The aim of our work was the evaluation of the immunoradiometric assay (IRMA) of two cytokeratinic markers, TPS and CYFRA 21.1, in clinical setting on non small cell lung cancer (NSCLC). Serum samples were obtained from 148 untreated NSCLC patients, 60 patients with non malignant lung diseases and 100 healthy subjects: TPS and CYFRA 21.1 serum levels were assayed by IRMA methods. Diagnostic performance of the markers was evaluated and the TPS and CYFRA 21.1 distribution analysed according to some different clinical and biological variables as histologi-cal subtypes, stage and survival time by using the Mann-Whitney "U"-test. Sensitivity, specificity and accuracy were 0.54 (80/148), 0.47 (28/60), 0.52 (108/208) and 0.73 (108/148), 0.74 (44/60), and 0.73 (152/208) for TPS and CYFRA 21.1 respectively. CYFRA 21.1 demonstrate a higher sensitivity than TPS in all stages of the disease and in the spinocellular and adenocarcinoma histological subtypes while TPS sensibility is higher in large cell carcinoma. The CYFRA 21.1 specificity is better than TPS probably by reason of its preferential distribution in respiratory epithelium. Both markers serum levels differ significantly between Stage Ⅰ-Ⅱ and Ⅳ and between Stage Ⅰ-Ⅱ-Ⅲa and Ⅲb-? but neither TPS nor CYFRA 21.1 can discriminate Stage Ⅲa from Ⅲb. No significant differences were found in the serum expression of the markers by the different histological subtypes. A value of both markers less than the selected cut-off is related to a longer survival of the patients apart from therapy (p < 0.05). Our conclusion supports similar behaviour of these markers in NSCLC and indicates CYFRA 21.1 as the more needed biochemical index to evaluate NSCLC patients.
机译:我们的工作目的是在非小细胞肺癌(NSCLC)的临床环境中评估两种细胞角蛋白标记TPS和CYFRA 21.1的免疫放射测定(IRMA)。分别从148例未经治疗的NSCLC患者,60例非恶性肺病患者和100例健康受试者中获取血清样品:通过IRMA方法测定TPS和CYFRA 21.1血清水平。使用Mann-Whitney“ U”检验,根据一些不同的临床和生物学变量,如组织学亚型,分期和生存时间,评估标记物的诊断性能,并分析TPS和CYFRA 21.1分布。对于TPS,敏感性,特异性和准确性分别为0.54(80/148),0.47(28/60),0.52(108/208)和0.73(108/148),0.74(44/60)和0.73(152/208)和CYFRA 21.1。 CYFRA 21.1在疾病的所有阶段以及在棘细胞和腺癌组织学亚型中均显示出比TPS更高的敏感性,而在大细胞癌中TPS的敏感性更高。 CYFRA 21.1特异性优于TPS,可能是由于其在呼吸道上皮细胞中的优先分布。两种标记物的血清水平在Ⅰ-Ⅱ期和Ⅳ期以及Ⅰ-Ⅱ-Ⅲa期和Ⅲb-b期之间显着不同。但是TPS和CYFRA 21.1都不能区分Ⅲa期和Ⅲb期。不同组织学亚型的标志物血清表达无明显差异。两种标记物的值均小于选定的临界值,这与除治疗外患者的生存期较长有关(p <0.05)。我们的结论支持这些标记在NSCLC中的相似行为,并表明CYFRA 21.1是评估NSCLC患者更需要的生化指标。

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