Nolen Brian M, Lomakin Aleksey, Marrangoni Adele, Velikokhatnaya Liudmila, Prosser Denise, Lokshin Anna E
University of Pittsburgh Cancer Institute, Hillman Cancer Center, Pittsburgh, Pennsylvania. Department of Medicine, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Department of Physics, Massachusetts Institute of Technology, Cambridge, Massachusetts.
Cancer Prev Res (Phila). 2015 Feb;8(2):111-9. doi: 10.1158/1940-6207.CAPR-14-0210. Epub 2014 Nov 21.
The early detection of lung cancer has the potential to greatly impact disease burden through the timely identification and treatment of affected individuals at a manageable stage of development. The insufficient specificity demonstrated by currently used screening and diagnostic techniques has led to intense investigation into biomarkers as diagnostic tools. Urine may represent a noninvasive alternative matrix for diagnostic biomarker development. We performed an analysis of 242 biomarkers in urines obtained from 83 patients with non-small cell lung carcinomas (NSCLC), 74 patients diagnosed with benign pulmonary conditions, and 77 healthy donors. A large number of significant alterations were observed between the NSCLC and control groups. A multivariate analysis identified a three-biomarker panel consisting of IGFBP-1, sIL-1Ra, CEACAM-1, which discriminated NSCLC from healthy controls with a sensitivity/specificity of 84/95 in an initial training set and 72/100 in an independent validation set. This panel performed well among multiple subtypes of NSCLC and early-stage disease but demonstrated only limited efficacy for the discrimination of NSCLC from benign controls and limited specificity for patients with several other cancers and tuberculosis. These findings demonstrate that urine biomarkers may provide screening and diagnostic properties which exceed those reported for serum biomarkers and approach a level necessary for further clinical development.
肺癌的早期检测有可能通过在可控制的发展阶段及时识别和治疗受影响个体,从而极大地影响疾病负担。目前使用的筛查和诊断技术所表现出的特异性不足,引发了对生物标志物作为诊断工具的深入研究。尿液可能是用于诊断生物标志物开发的一种非侵入性替代基质。我们对从83例非小细胞肺癌(NSCLC)患者、74例被诊断为良性肺部疾病的患者以及77名健康供体获取的尿液中的242种生物标志物进行了分析。在NSCLC组和对照组之间观察到大量显著变化。多变量分析确定了一个由胰岛素样生长因子结合蛋白-1(IGFBP-1)、可溶性白细胞介素-1受体拮抗剂(sIL-1Ra)、癌胚抗原相关细胞黏附分子-1(CEACAM-1)组成的三生物标志物组合,在初始训练集中,该组合区分NSCLC与健康对照的灵敏度/特异性为84/95,在独立验证集中为72/100。该组合在NSCLC的多种亚型和早期疾病中表现良好,但在区分NSCLC与良性对照方面仅显示出有限的功效,对其他几种癌症和结核病患者的特异性也有限。这些发现表明,尿液生物标志物可能提供超过血清生物标志物报道的筛查和诊断特性,并接近进一步临床开发所需的水平。