Serum Cripto-1 is a novel biomarker for non-small cell lung cancer diagnosis and prognosis

被引:23
作者
Xu, Chun Hua [1 ,2 ]
Wang, Yan [3 ]
Qian, Li Hua [4 ]
Yu, Li Ke [1 ,2 ]
Zhang, Xiu Wei [5 ]
Wang, Qing Bo [6 ]
机构
[1] Nanjing Chest Hosp, Dept Resp Med, 215 Guangzhou Rd, Nanjing, Jiangsu, Peoples R China
[2] Clin Ctr Nanjing Resp Dis & Imaging, Nanjing, Jiangsu, Peoples R China
[3] Nanjing Chest Hosp, Dept Radiol, Nanjing, Jiangsu, Peoples R China
[4] Nanjing Pukou Cent Hosp, Dept Resp Med, Nanjing, Jiangsu, Peoples R China
[5] Nanjing Jiangning Hosp, Dept Resp Med, Nanjing, Jiangsu, Peoples R China
[6] Nanjing Second Hosp, Dept Geriatr Med, Nanjing, Jiangsu, Peoples R China
关键词
Cripto-1; non-small cell lung cancer; diagnosis; prognosis; biomarker; EPITHELIAL-MESENCHYMAL TRANSITION; EGF-CFC FAMILY; CARCINOEMBRYONIC ANTIGEN; POOR-PROGNOSIS; BREAST-CANCER; TUMOR; CEA; OVEREXPRESSION; EMBRYOGENESIS; MARKERS;
D O I
10.1111/crj.12414
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
IntroductionCripto-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. ObjectivesThe aim of this study was to explore the diagnostic and prognostic value of serum CR-1 levels in patients with NSCLC. MethodsSerum 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. ResultsPatients 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). ConclusionsIn conclusion, measurement of serum CR-1 is a useful diagnostic and prognostic marker for NSCLC patients.
引用
收藏
页码:765 / 771
页数:7
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