Multicenter evaluation of a new progastrin-releasing peptide (ProGRP) immunoassay across Europe and China

被引:30
作者
Korse, Catharina M. [1 ]
Holdenrieder, Stefan [2 ,3 ]
Zhi, Xiu-yi [4 ]
Zhang, Xiaotong [5 ]
Qiu, Ling [5 ]
Geistanger, Andrea [6 ]
Lisy, Marcus-Rene [6 ]
Wehnl, Birgit [6 ]
van den Broek, Daan [1 ]
Escudero, Jose M. [7 ]
Standop, Jens [2 ,3 ]
Hu, Mu [4 ]
Molina, Rafael [7 ]
机构
[1] Netherlands Canc Inst, NL-1066 CX Amsterdam, Netherlands
[2] Univ Hosp Bonn, D-2553127 Bonn, Germany
[3] Ctr Integrat Oncol Cologne Bonn, D-2553127 Bonn, Germany
[4] Capital Med Univ, Xuanwu Hosp, Beijing 100053, Peoples R China
[5] Beijing Union Med Coll Hosp, Beijing 100730, Peoples R China
[6] Roche Diagnost GmbH, D-82377 Penzberg, Germany
[7] Univ Barcelona, Hosp Clin Barcelona, E-08036 Barcelona, Spain
关键词
Differential diagnosis; Immunoassay; Progastrin-releasing peptide; ProGRP; SCLC; Stability; CELL LUNG-CANCER; GLOMERULAR-FILTRATION-RATE; MALIGNANT DISEASES; DIAGNOSTIC-VALUE; TUMOR-MARKER; SERUM; BIOMARKERS; CARCINOMA; CHEMOTHERAPY; PREDICTION;
D O I
10.1016/j.cca.2014.09.015
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: We performed a multicenter evaluation of the Elecsys(R) progastrin-releasing peptide (ProGRP) immunoassay in Europe and China. Methods: The assay was evaluated at three European and two Chinese sites by imprecision, stability, method comparison and differentiation potential in lung cancer. Results: Intermediate imprecision across five analyte concentrations ranged from 2.2% to 6.0% coefficient of variation. Good stability for plasma and serum samples was shown for various storage conditions. There was excellent correlation between the Elecsys(R) and ARCHITECT assays in plasma (slope 1.02, intercept -2.72 pg/mL). The Elecsys(R) assay also showed good correlation between serum and plasma samples (slope 0.93, intercept 2.35 pg/mL; correlation coefficient 0.97). ProGRP differentiated small-cell and non-small-cell lung cancer (NSCLC; area under the curve 0.90, 95% CI 0.87-0.93; 78.3% sensitivity, 95% specificity; at 84 pg/mL), with no relevant effects of ethnicity, age, gender or smoking. Median ProGRP concentrations were low in benign diseases (38 pg/mL), other malignancies (40 pg/mL) or NSCLC (39 pg/mL), except chronic kidney disease above stage 3 (>100 pg/mL). Conclusions: Increased stability of the Elecsys(R) ProGRP assay in serum and plasma offers clear benefits over existing assays. This first evaluation of a ProGRP assay in China demonstrated comparable differentiation potential among different ethnicities. (C) 2014 The Authors. Published by Elsevier B.V.
引用
收藏
页码:388 / 395
页数:8
相关论文
共 44 条
[1]  
[Anonymous], 2011, FUJIREBIO PROGRP PAC
[2]  
[Anonymous], 2004, Evaluation of Precision Performance of Quantitative Measurement Methods
[3]  
Approved Guideline
[4]  
[Anonymous], 2009, ABBORT ARCHITECT PRO
[5]  
Biran H, 2014, CLIN ONCOL S, V32
[6]  
Carpenter J, 2000, STAT MED, V19, P1141, DOI 10.1002/(SICI)1097-0258(20000515)19:9<1141::AID-SIM479>3.0.CO
[7]  
2-F
[8]   Chemotherapy advances in small-cell lung cancer [J].
Chan, Bryan A. ;
Coward, Jermaine I. G. .
JOURNAL OF THORACIC DISEASE, 2013, 5 :S565-S578
[9]   COMPARING THE AREAS UNDER 2 OR MORE CORRELATED RECEIVER OPERATING CHARACTERISTIC CURVES - A NONPARAMETRIC APPROACH [J].
DELONG, ER ;
DELONG, DM ;
CLARKEPEARSON, DI .
BIOMETRICS, 1988, 44 (03) :837-845
[10]  
*EUR GROUP TUM MAR, 1999, ANTICANCER RES, V19, P2817