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Performance evaluation of CA242 by flow fluorescence assay
Carbohydrate antigen 24–2 (CA24–2) is usually used as a biomarker for the diagnosis of pancreatic cancer and colorectal cancer. Currentlly, a new quantitative assay kit for CA242 by flow fluorometry assay (FFA) was developed by Shanghai Tellgen Cooperation Co. Ltd. China. Therefore, we conducted the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8052011/ https://www.ncbi.nlm.nih.gov/pubmed/33847629 http://dx.doi.org/10.1097/MD.0000000000025301 |
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author | Hou, Yanyan Chen, Yongquan Sun, Jieli Geng, Jinting Jin, Hongwei Zhang, Zhongying |
author_facet | Hou, Yanyan Chen, Yongquan Sun, Jieli Geng, Jinting Jin, Hongwei Zhang, Zhongying |
author_sort | Hou, Yanyan |
collection | PubMed |
description | Carbohydrate antigen 24–2 (CA24–2) is usually used as a biomarker for the diagnosis of pancreatic cancer and colorectal cancer. Currentlly, a new quantitative assay kit for CA242 by flow fluorometry assay (FFA) was developed by Shanghai Tellgen Cooperation Co. Ltd. China. Therefore, we conducted the performance evaluation for it. According to the “Guiding principles on performance analysis of diagnostic reagents in vitro” and “American association of clinical laboratory standardization guidelines EP15-A2”, the accuracy, precision, linear range, reportable range, biological reference interval verification, carry-over contamination rate, anti-interference capability and cross reaction of the assay kit used in TESMI F3999-Luminex200 automatic immunoassay system were evaluated. In addition, the assay kit was performed in parallel to CanAg kit (CanAg Diagnostics Products Beijing Co., Ltd.) to analyze the correlation between the 2 kits. The bias of accuracy of the new assay kit was less than 12.5% and the coefficient of variations (CVs) of precision were all less than 10.0%. The linear range of CA242 concentration of the testing kit was between 3.46 U/ml and 434.76 U/ml and the reportable range was 6.00 to 535.13 U/ml. The CA242 reference interval 0.00 to 20.00 U/ml was suitable for use in laboratory. The carry-over contamination rate was −0.14%. Correlation analysis showed a satisfactory relevance and consistency (r = 0.982, P < .001) between the new assay kit and CanAg kit, with a regression equation Y = 1.0012X to 0.878 (R(2) = 0.9647, P < .001). No statistically significant difference between serum samples without interferences and samples containing lipemia, bilirubin and hemoglobin. And no cross reaction existed between the assay kit and the other tumor markers, such as carbohydrate antigen 125 (CA125), alpha-fetoprotein (AFP), and cytokeratin-19 soluble fragment (CYFRA21-1). The new CA242 quantitative assay kit possesses good detection performance when it is used in TESMI F3999-Luminex200 automatic immunoassay system, which can be used for the examination of CA242 in clinical practice. |
format | Online Article Text |
id | pubmed-8052011 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-80520112021-04-19 Performance evaluation of CA242 by flow fluorescence assay Hou, Yanyan Chen, Yongquan Sun, Jieli Geng, Jinting Jin, Hongwei Zhang, Zhongying Medicine (Baltimore) 3600 Carbohydrate antigen 24–2 (CA24–2) is usually used as a biomarker for the diagnosis of pancreatic cancer and colorectal cancer. Currentlly, a new quantitative assay kit for CA242 by flow fluorometry assay (FFA) was developed by Shanghai Tellgen Cooperation Co. Ltd. China. Therefore, we conducted the performance evaluation for it. According to the “Guiding principles on performance analysis of diagnostic reagents in vitro” and “American association of clinical laboratory standardization guidelines EP15-A2”, the accuracy, precision, linear range, reportable range, biological reference interval verification, carry-over contamination rate, anti-interference capability and cross reaction of the assay kit used in TESMI F3999-Luminex200 automatic immunoassay system were evaluated. In addition, the assay kit was performed in parallel to CanAg kit (CanAg Diagnostics Products Beijing Co., Ltd.) to analyze the correlation between the 2 kits. The bias of accuracy of the new assay kit was less than 12.5% and the coefficient of variations (CVs) of precision were all less than 10.0%. The linear range of CA242 concentration of the testing kit was between 3.46 U/ml and 434.76 U/ml and the reportable range was 6.00 to 535.13 U/ml. The CA242 reference interval 0.00 to 20.00 U/ml was suitable for use in laboratory. The carry-over contamination rate was −0.14%. Correlation analysis showed a satisfactory relevance and consistency (r = 0.982, P < .001) between the new assay kit and CanAg kit, with a regression equation Y = 1.0012X to 0.878 (R(2) = 0.9647, P < .001). No statistically significant difference between serum samples without interferences and samples containing lipemia, bilirubin and hemoglobin. And no cross reaction existed between the assay kit and the other tumor markers, such as carbohydrate antigen 125 (CA125), alpha-fetoprotein (AFP), and cytokeratin-19 soluble fragment (CYFRA21-1). The new CA242 quantitative assay kit possesses good detection performance when it is used in TESMI F3999-Luminex200 automatic immunoassay system, which can be used for the examination of CA242 in clinical practice. Lippincott Williams & Wilkins 2021-04-16 /pmc/articles/PMC8052011/ /pubmed/33847629 http://dx.doi.org/10.1097/MD.0000000000025301 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) |
spellingShingle | 3600 Hou, Yanyan Chen, Yongquan Sun, Jieli Geng, Jinting Jin, Hongwei Zhang, Zhongying Performance evaluation of CA242 by flow fluorescence assay |
title | Performance evaluation of CA242 by flow fluorescence assay |
title_full | Performance evaluation of CA242 by flow fluorescence assay |
title_fullStr | Performance evaluation of CA242 by flow fluorescence assay |
title_full_unstemmed | Performance evaluation of CA242 by flow fluorescence assay |
title_short | Performance evaluation of CA242 by flow fluorescence assay |
title_sort | performance evaluation of ca242 by flow fluorescence assay |
topic | 3600 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8052011/ https://www.ncbi.nlm.nih.gov/pubmed/33847629 http://dx.doi.org/10.1097/MD.0000000000025301 |
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