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A prognostic model for colorectal cancer based on CEA and a 48-multiplex serum biomarker panel

Mortality in colorectal cancer (CRC) remains high, resulting in 860,000 deaths annually. Carcinoembryonic antigen is widely used in clinics for CRC patient follow-up, despite carrying a limited prognostic value. Thus, an obvious need exists for multivariate prognostic models. We analyzed 48 biomarke...

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Autores principales: Björkman, Kajsa, Jalkanen, Sirpa, Salmi, Marko, Mustonen, Harri, Kaprio, Tuomas, Kekki, Henna, Pettersson, Kim, Böckelman, Camilla, Haglund, Caj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7900104/
https://www.ncbi.nlm.nih.gov/pubmed/33619304
http://dx.doi.org/10.1038/s41598-020-80785-1
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author Björkman, Kajsa
Jalkanen, Sirpa
Salmi, Marko
Mustonen, Harri
Kaprio, Tuomas
Kekki, Henna
Pettersson, Kim
Böckelman, Camilla
Haglund, Caj
author_facet Björkman, Kajsa
Jalkanen, Sirpa
Salmi, Marko
Mustonen, Harri
Kaprio, Tuomas
Kekki, Henna
Pettersson, Kim
Böckelman, Camilla
Haglund, Caj
author_sort Björkman, Kajsa
collection PubMed
description Mortality in colorectal cancer (CRC) remains high, resulting in 860,000 deaths annually. Carcinoembryonic antigen is widely used in clinics for CRC patient follow-up, despite carrying a limited prognostic value. Thus, an obvious need exists for multivariate prognostic models. We analyzed 48 biomarkers using a multiplex immunoassay panel in preoperative serum samples from 328 CRC patients who underwent surgery at Helsinki University Hospital between 1998 and 2003. We performed a multivariate prognostic forward-stepping background model based on basic clinicopathological data, and a multivariate machine-learned prognostic model based on clinicopathological data and biomarker variables, calculating the disease-free survival using the value of importance score. From the 48 analyzed biomarkers, only IL-8 emerged as a significant prognostic factor for CRC patients in univariate analysis (HR 4.88; 95% CI 2.00–11.92; p = 0.024) after correcting for multiple comparisons. We also developed a multivariate model based on all 48 biomarkers using a random survival forest analysis. Variable selection based on a minimal depth and the value of importance yielded two tentative candidate CRC prognostic markers: IL-2Ra and IL-8. A multivariate prognostic model using machine-learning technologies improves the prognostic assessment of survival among surgically treated CRC patients.
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spelling pubmed-79001042021-02-24 A prognostic model for colorectal cancer based on CEA and a 48-multiplex serum biomarker panel Björkman, Kajsa Jalkanen, Sirpa Salmi, Marko Mustonen, Harri Kaprio, Tuomas Kekki, Henna Pettersson, Kim Böckelman, Camilla Haglund, Caj Sci Rep Article Mortality in colorectal cancer (CRC) remains high, resulting in 860,000 deaths annually. Carcinoembryonic antigen is widely used in clinics for CRC patient follow-up, despite carrying a limited prognostic value. Thus, an obvious need exists for multivariate prognostic models. We analyzed 48 biomarkers using a multiplex immunoassay panel in preoperative serum samples from 328 CRC patients who underwent surgery at Helsinki University Hospital between 1998 and 2003. We performed a multivariate prognostic forward-stepping background model based on basic clinicopathological data, and a multivariate machine-learned prognostic model based on clinicopathological data and biomarker variables, calculating the disease-free survival using the value of importance score. From the 48 analyzed biomarkers, only IL-8 emerged as a significant prognostic factor for CRC patients in univariate analysis (HR 4.88; 95% CI 2.00–11.92; p = 0.024) after correcting for multiple comparisons. We also developed a multivariate model based on all 48 biomarkers using a random survival forest analysis. Variable selection based on a minimal depth and the value of importance yielded two tentative candidate CRC prognostic markers: IL-2Ra and IL-8. A multivariate prognostic model using machine-learning technologies improves the prognostic assessment of survival among surgically treated CRC patients. Nature Publishing Group UK 2021-02-22 /pmc/articles/PMC7900104/ /pubmed/33619304 http://dx.doi.org/10.1038/s41598-020-80785-1 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Björkman, Kajsa
Jalkanen, Sirpa
Salmi, Marko
Mustonen, Harri
Kaprio, Tuomas
Kekki, Henna
Pettersson, Kim
Böckelman, Camilla
Haglund, Caj
A prognostic model for colorectal cancer based on CEA and a 48-multiplex serum biomarker panel
title A prognostic model for colorectal cancer based on CEA and a 48-multiplex serum biomarker panel
title_full A prognostic model for colorectal cancer based on CEA and a 48-multiplex serum biomarker panel
title_fullStr A prognostic model for colorectal cancer based on CEA and a 48-multiplex serum biomarker panel
title_full_unstemmed A prognostic model for colorectal cancer based on CEA and a 48-multiplex serum biomarker panel
title_short A prognostic model for colorectal cancer based on CEA and a 48-multiplex serum biomarker panel
title_sort prognostic model for colorectal cancer based on cea and a 48-multiplex serum biomarker panel
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7900104/
https://www.ncbi.nlm.nih.gov/pubmed/33619304
http://dx.doi.org/10.1038/s41598-020-80785-1
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