Analysis of Tumor Markers in the Cytological Fluid Obtained from Computed Tomography-Guided Needle Aspiration Biopsy for the Diagnosis of Non-small Cell Lung Cancer

被引:19
作者
Hong, Yoo Jin [1 ,2 ]
Hur, Jin [1 ,2 ]
Lee, Hye-Jeong [1 ,2 ]
Nam, Ji Eun [1 ,2 ]
Kim, Young Jin [1 ,2 ]
Kim, Hua Sun [1 ,2 ]
Kim, Hee Yeong [1 ,2 ]
Kim, Se Kyu [3 ]
Chang, Joon [3 ]
Kim, Joo-Hang [3 ,4 ]
Chung, Kyung Young [5 ]
Choi, Byoung Wook [1 ,2 ]
Choe, Kyu Ok [1 ,2 ]
机构
[1] Yonsei Univ, Coll Med, Dept Radiol, Seoul 120752, South Korea
[2] Yonsei Univ, Coll Med, Res Inst Radiol Sci, Seoul 120752, South Korea
[3] Yonsei Univ, Coll Med, Dept Internal Med, Seoul 120752, South Korea
[4] Yonsei Univ, Coll Med, Yonsei Canc Ctr, Seoul 120752, South Korea
[5] Yonsei Univ, Coll Med, Dept Thorac & Cardiovasc Surg, Seoul 120752, South Korea
关键词
CYFRA; 21-1; CEA; SCC-Ag; Tumor marker; Cytological fluid; CT-guided needle aspiration biopsy (NAB); CARCINOEMBRYONIC ANTIGEN CEA; NEURON-SPECIFIC ENOLASE; PROGNOSTIC VALUE; CYFRA; 21-1; PULMONARY NODULES; PLASMA PROTEOME; NSE; SERUM; CLASSIFICATION; COMBINATION;
D O I
10.1097/JTO.0b013e31822462b1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The aim of this study was to prospectively assess whether analysis of the tumor markers cytokeratin 19 fragments (CYFRA 21-1), carcinoembryonic antigen (CEA), and squamous cell carcinoma (SCC) antigen in cytological fluid can improve the performance of computed tomography (CT)-guided needle aspiration biopsy (NAB) in the diagnosis of non-small cell lung cancer (NSCLC). Methods: A total of 100 patients (men: women = 41: 59, mean age: 63 years) with suspected malignant pulmonary lesions were prospectively enrolled for CT-guided NAB procedures. Levels of CYFRA 21-1, CEA, and SCC in the cytological fluid were measured by immunoradiometric assays. The cutoff value for tumor markers was selected on the basis of best accuracy through receiver operating characteristic curves. The sensitivity and areas under the curve (AUC) of NAB alone were compared with those of NAB combined with cytological tumor markers (CYFRA 21-1, CEA, and SCC). Results: Among 100 patients, 71 (71%) had NSCLC and 29 (29%) had benign lesions. The sensitivity, specificity, and accuracy for diagnosing NSCLC were 85.7%, 100%, and 89%, respectively, for NAB alone. The sensitivity increased significantly for NAB combined with a tumor marker compared with NAB alone (100% for CYFRA 21-1, 92.9% for CEA, and 94.2% for SCC; p = 0.001, p = 0.025, and p = 0.014, respectively). The AUC of NAB with CYFRA 21-1 was significantly larger than the AUC of NAB alone (p = 0.001). Conclusion: Evaluation of tumor markers CYFRA 21-1, CEA, and SCC in the cytological fluid can improve the diagnostic performance of CT-guided NAB for NSCLC. Of these markers, CYFRA 21-1 is the most useful cytological tumor marker.
引用
收藏
页码:1330 / 1335
页数:6
相关论文
共 32 条
[1]   The human plasma proteome - History, character, and diagnostic prospects [J].
Anderson, NL ;
Anderson, NG .
MOLECULAR & CELLULAR PROTEOMICS, 2002, 1 (11) :845-867
[2]   Prognostic value of combination of Cyfra 21-1, CEA and NSE in patients with advanced non-small cell lung cancer [J].
Barlési, F ;
Gimenez, C ;
Torre, JP ;
Doddoli, C ;
Mancini, J ;
Greillier, L ;
Roux, F ;
Kleisbauer, JP .
RESPIRATORY MEDICINE, 2004, 98 (04) :357-362
[3]   The new World Health Organization classification of lung tumours [J].
Brambilla, E ;
Travis, WD ;
Colby, TV ;
Corrin, B ;
Shimosato, Y .
EUROPEAN RESPIRATORY JOURNAL, 2001, 18 (06) :1059-1068
[4]   Diagnostic and prognostic value of Cyfra 21-1 compared with other tumour markers in patients with non-small cell lung cancer: A prospective study of 116 patients [J].
Brechot, JM ;
Chevret, S ;
Nataf, J ;
LeGall, C ;
Fretault, J ;
Rochemaure, J ;
Chastang, C .
EUROPEAN JOURNAL OF CANCER, 1997, 33 (03) :385-391
[5]   Proteomic approaches in lung cancer biomarker development [J].
Cho, Je-Yoel ;
Sung, Hye-Jin .
EXPERT REVIEW OF PROTEOMICS, 2009, 6 (01) :27-42
[6]   Identification of serum amyloid a protein as a potentially useful biomarker to monitor relapse of nasopharyngeal cancer by serum proteomic profiling [J].
Cho, WCS ;
Yip, TTC ;
Yip, C ;
Yip, V ;
Thulasiraman, V ;
Ngan, RKC ;
Yip, TT ;
Lau, WH ;
An, JSK ;
Law, SCK ;
Cheng, WW ;
Ma, VWS ;
Lim, CKP .
CLINICAL CANCER RESEARCH, 2004, 10 (01) :43-52
[7]   ROLE OF PERCUTANEOUS FINE-NEEDLE ASPIRATION BIOPSY IN SUSPECTED INTRATHORACIC MALIGNANCY [J].
COLQUHOUN, SD ;
ROSENTHAL, DL ;
MORTON, DL .
ANNALS OF THORACIC SURGERY, 1991, 51 (03) :390-393
[8]  
Ferrer J, 1999, CANCER-AM CANCER SOC, V86, P1488, DOI 10.1002/(SICI)1097-0142(19991015)86:8<1488::AID-CNCR15>3.0.CO
[9]  
2-Y
[10]   PERCUTANEOUS NEEDLE-BIOPSY OF THORACIC LESIONS - EVALUATION OF 300 BIOPSIES [J].
FLOWER, CDR ;
VERNEY, GI .
CLINICAL RADIOLOGY, 1979, 30 (02) :215-218