A multi-analyte serum test for the detection of non-small cell lung cancer

被引:32
作者
Farlow, E. C. [2 ]
Vercillo, M. S. [2 ]
Coon, J. S. [1 ]
Basu, S. [3 ]
Kim, A. W. [4 ]
Faber, L. P. [4 ]
Warren, W. H. [4 ]
Bonomi, P. [5 ]
Liptay, M. J. [4 ]
Borgia, J. A. [1 ,6 ]
机构
[1] Rush Univ, Med Ctr, Dept Pathol, Jelke S Ctr 532, Chicago, IL 60612 USA
[2] Rush Univ, Med Ctr, Dept Gen Surg, Jelke S Ctr 785, Chicago, IL 60612 USA
[3] Rush Univ, Med Ctr, Dept Preventat Med, Chicago, IL 60612 USA
[4] Rush Univ, Med Ctr, Dept Thorac Surg, Chicago, IL 60612 USA
[5] Rush Univ, Med Ctr, Dept Med Oncol, Chicago, IL 60612 USA
[6] Rush Univ, Med Ctr, Dept Biochem, Chicago, IL 60612 USA
关键词
Luminex; serum; non-small cell lung cancer; diagnosis; PROGNOSTIC-SIGNIFICANCE; TUMOR-MARKERS; DIAGNOSIS; AUTOANTIBODIES; EXPRESSION; BIOMARKERS; PROTEIN;
D O I
10.1038/sj.bjc.6605865
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: In this study, we appraised a wide assortment of biomarkers previously shown to have diagnostic or prognostic value for non-small cell lung cancer (NSCLC) with the intent of establishing a multi-analyte serum test capable of identifying patients with lung cancer. METHODS: Circulating levels of 47 biomarkers were evaluated against patient cohorts consisting of 90 NSCLC and 43 non-cancer controls using commercial immunoassays. Multivariate statistical methods were used on all biomarkers achieving statistical relevance to define an optimised panel of diagnostic biomarkers for NSCLC. The resulting biomarkers were fashioned into a classification algorithm and validated against serum from a second patient cohort. RESULTS: A total of 14 analytes achieved statistical relevance upon evaluation. Multivariate statistical methods then identified a panel of six biomarkers (tumour necrosis factor-alpha, CYFRA 21-1, interleukin-1ra, matrix metalloproteinase-2, monocyte chemotactic protein-1 and sE-selectin) as being the most efficacious for diagnosing early stage NSCLC. When tested against a second patient cohort, the panel successfully classified 75 of 88 patients. CONCLUSIONS: Here, we report the development of a serum algorithm with high specificity for classifying patients with NSCLC against cohorts of various 'high-risk' individuals. A high rate of false positives was observed within the cohort in which patients had non-neoplastic lung nodules, possibly as a consequence of the inflammatory nature of these conditions. British Journal of Cancer (2010) 103, 1221-1228. doi:10.1038/sj.bjc.6605865 www.bjcancer.com Published online 21 September 2010 (C) 2010 Cancer Research UK
引用
收藏
页码:1221 / 1228
页数:8
相关论文
共 32 条
[1]  
[Anonymous], R LANG ENV STAT COMP
[2]   Screening for non-small cell lung cancer [J].
Ashton, RW ;
Jett, JR .
SEMINARS IN ONCOLOGY, 2005, 32 (03) :253-258
[3]   Clinical value of CYFRA 21.1, carcinoembryonic antigen, neurone-specific enolase, tissue polypeptide specific antigen and tissue polypeptide antigen in the diagnosis of lung cancer [J].
Bates, J ;
Rutherford, R ;
Divilly, M ;
Finn, J ;
Grimes, H ;
O'Muircheartaigh, I ;
Gilmartin, JJ .
EUROPEAN RESPIRATORY JOURNAL, 1997, 10 (11) :2535-2538
[4]   SmcHD1, containing a structural-maintenance-of-chromosomes hinge domain, has a critical role in X inactivation [J].
Blewitt, Marnie E. ;
Gendrel, Anne-Valerie ;
Pang, Zhenyi ;
Sparrow, Duncan B. ;
Whitelaw, Nadia ;
Craig, Jeffrey M. ;
Apedaile, Anwyn ;
Hilton, Douglas J. ;
Dunwoodie, Sally L. ;
Brockdorff, Neil ;
Kay, Graham F. ;
Whitelaw, Emma .
NATURE GENETICS, 2008, 40 (05) :663-669
[5]   Prognostic significance of osteopontin expression in early-stage non-small-cell lung cancer [J].
Boldrini, L ;
Donati, V ;
Dell'Omodarme, M ;
Prati, MC ;
Faviana, P ;
Camacci, T ;
Lucchi, M ;
Mussi, A ;
Santoro, M ;
Basolo, F ;
Fontanini, G .
BRITISH JOURNAL OF CANCER, 2005, 93 (04) :453-457
[6]   Establishment of a Multi-Analyte Serum Biomarker Panel to Identify Lymph Node Metastases in Non-small Cell Lung Cancer [J].
Borgia, Jeffrey A. ;
Basu, Sanjib ;
Faber, L. Penfield ;
Kim, Anthony W. ;
Coon, John S. ;
Kaiser-Walters, Kelly A. ;
Fhied, Cristina ;
Thomas, Sherene ;
Rouhi, Omid ;
Warren, William H. ;
Bonomi, Philip ;
Liptay, Michael J. .
JOURNAL OF THORACIC ONCOLOGY, 2009, 4 (03) :338-347
[7]   Random forests [J].
Breiman, L .
MACHINE LEARNING, 2001, 45 (01) :5-32
[8]   Autoantibodies in lung cancer:: possibilities for early detection and subsequent cure [J].
Chapman, C. J. ;
Murray, A. ;
McElveen, J. E. ;
Sahin, U. ;
Luxemburger, U. ;
Tuereci, Oe ;
Wiewrodt, R. ;
Barnes, A. C. ;
Robertson, J. F. .
THORAX, 2008, 63 (03) :228-233
[9]  
Chen Feng, 2008, Sichuan Da Xue Xue Bao Yi Xue Ban, V39, P832
[10]   Serum protein expression predicts recurrence in patients with early-stage lung cancer after resection [J].
D'Amico, Thomas A. ;
Brooks, Kelli R. ;
Joshi, Mary-Beth Moore ;
Conlon, Debbi ;
Herndon, James, II ;
Petersen, Rebecca P. ;
Harpole, David H., Jr. .
ANNALS OF THORACIC SURGERY, 2006, 81 (06) :1982-1987