Xu Chun Hua, Wang Yan, Qian Li Hua, Yu Li Ke, Zhang Xiu Wei, Wang Qing Bo
Department of Respiratory Medicine, Nanjing Chest Hospital, Nanjing, China.
Clinical Center of Nanjing Respiratory Diseases and Imaging, Nanjing, China.
Clin Respir J. 2017 Nov;11(6):765-771. doi: 10.1111/crj.12414. Epub 2016 Jan 25.
Cripto-1 (CR-1) is highly expressed in several different types of human tumors. However, the clinical significance of CR-1 expression in serum specimens from non-small cell lung cancer (NSCLC) patients has not yet been determined.
The aim of this study was to explore the diagnostic and prognostic value of serum CR-1 levels in patients with NSCLC.
Serum specimens from 592 NSCLC patients, 180 benign lung disease patients and 240 healthy controls were collected. The concentrations of CR-1 were measured by sandwich enzyme-linked immunosorbent assay.
Patients with NSCLC had higher serum CR-1 levels than the controls (P < 0.01) and patients with benign lung diseases (P < 0.01). When a cutoff point of 1.8 ng/mL was selected (diagnostic specificity 95%), the diagnostic sensitivity for NSCLC is 56.8%. About 37.5% of carcinoembryonic antigen (CEA)-negative lung cancer patients were CR-1 positive at 95% specificity. In patients with stage I/II lung cancer, use of these two markers in combination results in almost 21% increase in sensitivity, at 95% specificity, compared with CEA alone. Uni-variate analysis revealed that NSCLC patients with positive CR-1 had a shorter overall survival (OS) and progression-free survival (PFS) than those with negative CR-1 [hazard ratio (HR) of 2.93, P = 0.005; HR of 2.12, P = 0.005]. Cox multi-variate analysis indicated that CR-1 was an independent prognostic indicator of PFS and OS (HR of 1.91, P = 0.006; HR of 1.82, P = 0.007). Kaplan-Meier survival curves further confirmed that patients with negative CR-1 had longer PFS and OS (P = 0.026 and P = 0.011, respectively).
In conclusion, measurement of serum CR-1 is a useful diagnostic and prognostic marker for NSCLC patients.
Cripto-1(CR-1)在几种不同类型的人类肿瘤中高表达。然而,CR-1在非小细胞肺癌(NSCLC)患者血清标本中的临床意义尚未确定。
本研究旨在探讨血清CR-1水平在NSCLC患者中的诊断和预后价值。
收集了592例NSCLC患者、180例良性肺病患者和240例健康对照者的血清标本。采用夹心酶联免疫吸附测定法测量CR-1的浓度。
NSCLC患者的血清CR-1水平高于对照组(P<0.01)和良性肺病患者(P<0.01)。当选择1.8 ng/mL的临界值时(诊断特异性为95%),NSCLC的诊断敏感性为56.8%。在95%的特异性水平下,约37.5%的癌胚抗原(CEA)阴性肺癌患者CR-1呈阳性。在I/II期肺癌患者中,与单独使用CEA相比,联合使用这两种标志物在95%的特异性水平下可使敏感性提高近21%。单因素分析显示,CR-1阳性的NSCLC患者的总生存期(OS)和无进展生存期(PFS)短于CR-1阴性的患者[风险比(HR)为2.93,P=0.005;HR为2.12,P=0.005]。Cox多因素分析表明,CR-1是PFS和OS的独立预后指标(HR为1.91,P=0.006;HR为1.82,P=0.007)。Kaplan-Meier生存曲线进一步证实,CR-1阴性的患者具有更长的PFS和OS(分别为P=0.026和P=0.011)。
总之,血清CR-1的检测是NSCLC患者有用的诊断和预后标志物。