Performance Evaluation of an Enzyme-Linked Immunosorbent Assay for Seven Autoantibodies in Lung Cancer

被引:5
|
作者
Mu Yin-Yu [1 ]
Xie Fu-Yi [1 ]
Wang Fei-Bo [1 ]
Zhang Ri-Yi [1 ]
Yuan Xiao-Lin [2 ]
机构
[1] Li Huili Hosp, Ningbo Med Ctr, Dept Clin Lab, Ningbo 315040, Zhejiang, Peoples R China
[2] Hangzhou Canc Probe Biotech Co, Hangzhou, Zhejiang, Peoples R China
关键词
enzyme-linked immunosorbent assay; autoantibody; evaluation; kit; performance;
D O I
10.7754/Clin.Lab.2018.180930
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: To verify and evaluate the performance characteristics of an enzyme-linked immunosorbent assay (ELISA) assay kit (Hangzhou Cancer probe Biotech Company) for seven autoantibodies (7-AABS), including p53, GAGE7, PGP9.5, CAGE, MAGEA1, SOX2, and GBU4-5. Methods: Evaluation was carried out according to "Guidelines for performance evaluation of in vitro diagnostic reagent". The performance parameters included detection limit, reportable range, precision, accuracy, and method comparison. Results: The detection limit was less than 3.75 U/mL. Reportable range was from 3.75 U/mL to 60 U/mL. The coefficient of variations (CVs) of within-run of 7-AABS were 5.15% - 10.13%, and between-run of CVs were 3.41% - 8.80%. For accuracy verification, the relative deviations (Bias) were all lower than 15% in the indicated concentration range. The sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and accuracy were 35.9%, 90.0%, 80.3%, 55.3%, 61.3%, respectively. Conclusions: Overall, the verification study demonstrated the performance of the kit meets the testing requirements. It is qualified for clinical applications.
引用
收藏
页码:603 / 608
页数:6
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