标记免疫分析与临床2024,Vol.31Issue(8) :1495-1499.DOI:10.11748/bjmy.issn.1006-1703.2024.08.023

血清CEA、NSE、SCC-Ag和CA125联合检验在非小细胞肺癌中的诊断价值

The Diagnostic Value of Serum CEA,NSE,SCC-Ag,and CA125 Combined Test in Non-small Cell Lung Cancer

韩菊玲 王婧 郭英 范志刚
标记免疫分析与临床2024,Vol.31Issue(8) :1495-1499.DOI:10.11748/bjmy.issn.1006-1703.2024.08.023

血清CEA、NSE、SCC-Ag和CA125联合检验在非小细胞肺癌中的诊断价值

The Diagnostic Value of Serum CEA,NSE,SCC-Ag,and CA125 Combined Test in Non-small Cell Lung Cancer

韩菊玲 1王婧 1郭英 1范志刚2
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作者信息

  • 1. 三二○一医院呼吸与危重症医学科,陕西汉中 723000
  • 2. 三二○一医院肿瘤内一科,陕西汉中 723000
  • 折叠

摘要

目的 探究血清癌胚抗原(CEA)、神经特异性烯醇化酶(NSE)、鳞癌相关抗原(SCC-Ag)、糖类抗原125(CA125)联合检验在非小细胞肺癌(NSCLC)中的诊断价值.方法 选取2021年1月至2024年1月在本院就诊的110例NSCLC患者作为NSCLC组,另选取同期在本院体检的健康志愿者50例作为对照组.比较2组血清CEA、NSE、SCC-Ag以及CA125水平的差异;依据病理T分期将NSCLC组患者分为T1期、T2期、T3期3个不同亚组,依据病理N分期将NSCLC患者分为N0期、N1期、N2期3个不同亚组,比较不同病理T分期、N分期NSCLC患者血清CEA、NSE、SCC-Ag以及CA125水平的差异;并绘制ROC曲线分析上述指标单一及联合在NSCLC诊断中的效能.结果 在CEA、NSE、SCC-Ag、CA125水平比较上,NSCLC组均高于对照组(P<0.05).血清CEA、NSE、SCC-Ag、CA125水平均随NSCLC患者病理T分期的递增而升高(P<0.05),且各分期结果比较差异有统计学意义(P<0.05).血清CEA、NSE、SCC-Ag、CA125水平均随NSCLC患者病理N分期的递增而升高(P<0.05),且各分期结果比较差异有统计学意义(P<0.05).CEA、NSE、SCC-Ag、CA125诊断NSCLC的AUC分别为 0.869(95%CI 为 0.827~0.917)、0.873(95%CI 为 0.812~0.921)、0.854(95%CI 为 0.789~0.905)、0.826(95%CI为 0.758~0.881),4 者联合诊断 NSCLC 的 AUC 为 0.982(95%CI 为 0.947~0.996),均较 CEA、NSE、SCC-Ag、CA125 各单一指标效能更高(Z=4.152、4.268、4.663、4.783,P<0.001).结论 血清 CEA、NSE、SCC-Ag、CA125 与 NSCLC病理类型、淋巴结转移数目、EGFR基因型等存在关系,且通过联合检测CEA、NSE、SCC-Ag、CA125水平可有效提高临床诊断NSCLC的效能.

Abstract

Objective To explore the diagnostic value of a combined test of serum carcinoembryonic antigen(CEA),neural specific enolase(NSE),squamous cell carcinoma associated antigen(SCC-Ag),and carbohydrate antigen 125(CA125)in non-small cell lung cancer(NSCLC).Methods 110 NSCLC patients who visited our hospital from January,2021 to January,2024 were selected as the NSCLC group,while 50 healthy volunteers who underwent physical examinations at our hospital during the same period were selected as the control group.We identified and evaluated differences in serum CEA,NSE,SCC-Ag,and CA125 levels between these two groups;According to the pathological T stage,NSCLC patients were divided into three different subgroups:T1,T2,and T3.Based on the pathological N stage,NSCLC patients were divided into three different subgroups:N0,N1,and N2.The differences in serum CEA,NSE,SCC-Ag,and CA125 levels among NSCLC patients with different pathological T stages and N stages were identified and evaluated;ROC curves were drawn to analyze the effectiveness of single and combined indicators in the diagnosis of NSCLC.Results In comparison of CEA,NSE,SCC-Ag,and CA125 levels,the NSCLC group was higher than the control group(P<0.05).Levels of serum CEA,NSE,SCC-Ag,and CA125 all increased with the increase of pathological T stage in NSCLC patients(P<0.05),and the differences in results of each stage were statistically significant(P<0.05).Levels of serum CEA,NSE,SCC-Ag,and CA125 all increased with the increase of pathological N-stage in NSCLC patients(P<0.05),and the differences in results of each stage were statistically significant(P<0.05).AUCs of CEA,NSE,SCC-Ag,and CA125 in diagnosing NSCLC were 0.869(95%CI,0.827-0.917),0.873(95%CI,0.812-0.921),0.854(95%CI,0.789-0.905),and 0.826(95%CI,0.758-0.881),respectively.AUC of four markers combined in diagnosing NSCLC was 0.982(95%CI,0.947-0.996),all of which were more effective than the single indicators of CEA,NSE,SCC-Ag,and CA125(Z=4.152,4.268,4.663,4.783,P<0.001).Conclusion There is an association between serum CEA,NSE,SCC-Ag,CA125 and the pathological type,number of lymph node metastases,and EGFR genotype of NSCLC.Combined detection of CEA,NSE,SCC-Ag,and CA125 levels can effectively improve the clinical diagnostic efficiency of NSCLC.

关键词

非小细胞肺癌/癌胚抗原/神经特异性烯醇化酶/鳞癌相关抗原/糖类抗原125/TNM分期

Key words

Non-small cell lung cancer/Carcinoembryonic antigen/Neurospecific enolase/Squamous cell carcinoma associated antigens/Carbohydrate antigen 125/TNM staging

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基金项目

陕西省重点研发计划项目(2021SF-044)

出版年

2024
标记免疫分析与临床
中国同辐股份有限公司

标记免疫分析与临床

CSTPCD
影响因子:0.978
ISSN:1006-1703
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