Free DNA and carcinoembryonic antigen serum levels: An important combination for diagnosis of colorectal cancer

被引:106
作者
Flamini, Emanuela
Mercatali, Laura
Nanni, Oriana
Calistri, Daniele
Nunziatini, Roberta
Zoli, Wainer
Rosetti, Paola
Gardini, Nice
Lattuneddu, Arturo
MariaVerdecchia, Giorgio
Amadori, Dino
机构
[1] Morgagni Pierantoni Hosp, Dept Med Oncol, I-47100 Forli, Italy
[2] Morgagni Pierantoni Hosp, Dept Gen Surg 1, I-47100 Forli, Italy
[3] Morgagni Pierantoni Hosp, Dept Gen Surg 2, I-47100 Forli, Italy
[4] Morgagni Pierantoni Hosp, Chem Clin Anal Lab, I-47100 Forli, Italy
[5] Morgagni Pierantoni Hosp, Blood Transfus Unit, I-47100 Forli, Italy
[6] Ist Oncol Romagnolo, Forli, Italy
[7] Ist Sci Romagnolo Studio & Cura Tumori, Meldola, Italy
关键词
D O I
10.1158/1078-0432.CCR-06-1931
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The identification of new molecular markers for the early detection of colorectal cancer has become an important objective. We compared the sensitivity and specificity of free circulating DNA with that of the more conventional carcinoembryonic antigen (CEA) and evaluated the two markers in combination. Experimental Design: The study was carried out on 75 healthy donors and 75 colorectal cancer patients. Free DNA was determined in serum with quantitative PCR analysis. The diagnostic accuracy of each assay was calculated using receiver operating characteristic (ROC) curves. The diagnostic relevance of the two-marker combination was analyzed by the logistic regression model. Results: Median free DNA concentration was similar to 5-fold higher in patients than in healthy donors (P < 0.001). The area under the ROC curve was 0.86, and when 12.5 ng/mL was used as cutoff, 81.3% sensitivity and 73.3% specificity were observed for the overall series. As CEA and free DNA provided independent diagnostic information, they were also considered in combination. ROC curve analysis of the combined CEA and free DNA algorithms showed a higher diagnostic capacity (area under the ROC curve, 0.92) than that of markers considered singly, with 84% sensitivity and 88% specificity. Conclusions: Free circulating DNA, especially when used in combination with CEA, represents a potentially useful tool for the diagnosis of early-stage colorectal cancer.
引用
收藏
页码:6985 / 6988
页数:4
相关论文
共 28 条
[11]  
Gai S, 2004, BRIT J CANCER, V90, P1211
[12]  
García-Olmo D, 2001, ANN NY ACAD SCI, V945, P265
[13]   Circulating deoxyribonucleic acid as prognostic marker in non-small-cell lung cancer patients undergoing chemotherapy [J].
Gautschi, O ;
Bigosch, C ;
Huegli, B ;
Jermann, M ;
Marx, A ;
Chassé, E ;
Ratschiller, D ;
Weder, W ;
Joerger, M ;
Betticher, DC ;
Stahel, RA ;
Ziegler, A .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (20) :4157-4164
[14]   Molecular detection of micrometastatic breast cancer in histopathology-negative axillary lymph nodes correlates with traditional predictors of prognosis -: An interim analysis of a prospective multi-institutional cohort study [J].
Gillanders, WE ;
Mikhitarian, K ;
Hebert, R ;
Mauldin, PD ;
Palesch, Y ;
Walters, C ;
Urist, MM ;
Mann, GB ;
Doherty, G ;
Herrmann, VM ;
Hill, AD ;
Eremin, O ;
El-Sheemy, M ;
Orr, RK ;
Valle, AA ;
Henderson, MA ;
Dewitty, RL ;
Sugg, SL ;
Frykberg, E ;
Yeh, K ;
Bell, RM ;
Metcalf, JS ;
Elliott, BM ;
Brothers, T ;
Robison, J ;
Mitas, M ;
Cole, DJ .
ANNALS OF SURGERY, 2004, 239 (06) :828-837
[15]  
HEID CA, 1996, GENOME RES, V8, P2883
[16]  
Johnson PJ, 2002, CLIN CHEM, V48, P1186
[17]   Somatic mutation screening: Identification of individuals harboring K-ras mutations with the use of plasma DNA [J].
Kopreski, MS ;
Benko, FA ;
Borys, DJ ;
Khan, A ;
McGarrity, TJ ;
Gocke, CD .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2000, 92 (11) :918-923
[18]  
LEON SA, 1977, CANCER RES, V37, P646
[19]   BASIC PRINCIPLES OF ROC ANALYSIS [J].
METZ, CE .
SEMINARS IN NUCLEAR MEDICINE, 1978, 8 (04) :283-298
[20]   Global cancer statistics, 2002 [J].
Parkin, DM ;
Bray, F ;
Ferlay, J ;
Pisani, P .
CA-A CANCER JOURNAL FOR CLINICIANS, 2005, 55 (02) :74-108