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Prospective evaluation of 64 serum autoantibodies as biomarkers for early detection of colorectal cancer in a true screening setting

Novel blood-based screening tests are strongly desirable for early detection of colorectal cancer (CRC). We aimed to identify and evaluate autoantibodies against tumor-associated antigens as biomarkers for early detection of CRC. 380 clinically identified CRC patients and samples of participants wit...

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Autores principales: Chen, Hongda, Werner, Simone, Butt, Julia, Zörnig, Inka, Knebel, Phillip, Michel, Angelika, Eichmüller, Stefan B., Jäger, Dirk, Waterboer, Tim, Pawlita, Michael, Brenner, Hermann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4941325/
https://www.ncbi.nlm.nih.gov/pubmed/26909861
http://dx.doi.org/10.18632/oncotarget.7500
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author Chen, Hongda
Werner, Simone
Butt, Julia
Zörnig, Inka
Knebel, Phillip
Michel, Angelika
Eichmüller, Stefan B.
Jäger, Dirk
Waterboer, Tim
Pawlita, Michael
Brenner, Hermann
author_facet Chen, Hongda
Werner, Simone
Butt, Julia
Zörnig, Inka
Knebel, Phillip
Michel, Angelika
Eichmüller, Stefan B.
Jäger, Dirk
Waterboer, Tim
Pawlita, Michael
Brenner, Hermann
author_sort Chen, Hongda
collection PubMed
description Novel blood-based screening tests are strongly desirable for early detection of colorectal cancer (CRC). We aimed to identify and evaluate autoantibodies against tumor-associated antigens as biomarkers for early detection of CRC. 380 clinically identified CRC patients and samples of participants with selected findings from a cohort of screening colonoscopy participants in 2005–2013 (N=6826) were included in this analysis. Sixty-four serum autoantibody markers were measured by multiplex bead-based serological assays. A two-step approach with selection of biomarkers in a training set, and validation of findings in a validation set, the latter exclusively including participants from the screening setting, was applied. Anti-MAGEA4 exhibited the highest sensitivity for detecting early stage CRC and advanced adenoma. Multi-marker combinations substantially increased sensitivity at the price of a moderate loss of specificity. Anti-TP53, anti-IMPDH2, anti-MDM2 and anti-MAGEA4 were consistently included in the best-performing 4-, 5-, and 6-marker combinations. This four-marker panel yielded a sensitivity of 26% (95% CI, 13–45%) for early stage CRC at a specificity of 90% (95% CI, 83–94%) in the validation set. Notably, it also detected 20% (95% CI, 13–29%) of advanced adenomas. Taken together, the identified biomarkers could contribute to the development of a useful multi-marker blood-based test for CRC early detection.
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spelling pubmed-49413252016-07-19 Prospective evaluation of 64 serum autoantibodies as biomarkers for early detection of colorectal cancer in a true screening setting Chen, Hongda Werner, Simone Butt, Julia Zörnig, Inka Knebel, Phillip Michel, Angelika Eichmüller, Stefan B. Jäger, Dirk Waterboer, Tim Pawlita, Michael Brenner, Hermann Oncotarget Research Paper Novel blood-based screening tests are strongly desirable for early detection of colorectal cancer (CRC). We aimed to identify and evaluate autoantibodies against tumor-associated antigens as biomarkers for early detection of CRC. 380 clinically identified CRC patients and samples of participants with selected findings from a cohort of screening colonoscopy participants in 2005–2013 (N=6826) were included in this analysis. Sixty-four serum autoantibody markers were measured by multiplex bead-based serological assays. A two-step approach with selection of biomarkers in a training set, and validation of findings in a validation set, the latter exclusively including participants from the screening setting, was applied. Anti-MAGEA4 exhibited the highest sensitivity for detecting early stage CRC and advanced adenoma. Multi-marker combinations substantially increased sensitivity at the price of a moderate loss of specificity. Anti-TP53, anti-IMPDH2, anti-MDM2 and anti-MAGEA4 were consistently included in the best-performing 4-, 5-, and 6-marker combinations. This four-marker panel yielded a sensitivity of 26% (95% CI, 13–45%) for early stage CRC at a specificity of 90% (95% CI, 83–94%) in the validation set. Notably, it also detected 20% (95% CI, 13–29%) of advanced adenomas. Taken together, the identified biomarkers could contribute to the development of a useful multi-marker blood-based test for CRC early detection. Impact Journals LLC 2016-02-19 /pmc/articles/PMC4941325/ /pubmed/26909861 http://dx.doi.org/10.18632/oncotarget.7500 Text en Copyright: © 2016 Chen et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Chen, Hongda
Werner, Simone
Butt, Julia
Zörnig, Inka
Knebel, Phillip
Michel, Angelika
Eichmüller, Stefan B.
Jäger, Dirk
Waterboer, Tim
Pawlita, Michael
Brenner, Hermann
Prospective evaluation of 64 serum autoantibodies as biomarkers for early detection of colorectal cancer in a true screening setting
title Prospective evaluation of 64 serum autoantibodies as biomarkers for early detection of colorectal cancer in a true screening setting
title_full Prospective evaluation of 64 serum autoantibodies as biomarkers for early detection of colorectal cancer in a true screening setting
title_fullStr Prospective evaluation of 64 serum autoantibodies as biomarkers for early detection of colorectal cancer in a true screening setting
title_full_unstemmed Prospective evaluation of 64 serum autoantibodies as biomarkers for early detection of colorectal cancer in a true screening setting
title_short Prospective evaluation of 64 serum autoantibodies as biomarkers for early detection of colorectal cancer in a true screening setting
title_sort prospective evaluation of 64 serum autoantibodies as biomarkers for early detection of colorectal cancer in a true screening setting
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4941325/
https://www.ncbi.nlm.nih.gov/pubmed/26909861
http://dx.doi.org/10.18632/oncotarget.7500
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