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Opportunistic screening and survival prediction of digestive cancers by the combination of blood mSEPT9 with protein markers

BACKGROUND: The early detection of digestive cancers and precancerous diseases remains a significant challenge. This study aimed to investigate the performance of the blood methylated SEPT9 (mSEPT9) assay, and the combination of this assay with serum protein markers, in hospital-based opportunistic...

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Autores principales: Song, Lele, Chen, Yan, Gong, Yuan, Wan, Jun, Guo, Shaohua, Liu, Hongyi, Li, Yuemin, Zeng, Zhen, Lu, Yinying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7745555/
https://www.ncbi.nlm.nih.gov/pubmed/33403008
http://dx.doi.org/10.1177/1758835920962966
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author Song, Lele
Chen, Yan
Gong, Yuan
Wan, Jun
Guo, Shaohua
Liu, Hongyi
Li, Yuemin
Zeng, Zhen
Lu, Yinying
author_facet Song, Lele
Chen, Yan
Gong, Yuan
Wan, Jun
Guo, Shaohua
Liu, Hongyi
Li, Yuemin
Zeng, Zhen
Lu, Yinying
author_sort Song, Lele
collection PubMed
description BACKGROUND: The early detection of digestive cancers and precancerous diseases remains a significant challenge. This study aimed to investigate the performance of the blood methylated SEPT9 (mSEPT9) assay, and the combination of this assay with serum protein markers, in hospital-based opportunistic screening strategies for digestive cancers. METHODS: Opportunistic screening was performed in the participating hospitals on outpatients and inpatients who met specific inclusion criteria. We recruited a total of 2030 subjects, including 764 cancer patients [291 colorectal cancer (CRC), 239 gastric cancer (GC), 106 esophageal cancer (EC), and 128 hepatocellular carcinoma (HCC)], 423 subjects with precancerous diseases, and 843 normal subjects. All samples were transported to an authenticated clinical laboratory where the mSEPT9 tests were performed. RESULTS: When used separately, the mSEPT9 detected CRC, GC, EC, and HCC, with a sensitivity of 76.6% [area under the receiver operating characteristic curve (AUC) = 0.86)], 47.7% (AUC = 0.76), 42.6% (AUC = 0.69), and 76.7% (AUC = 0.85) and a specificity of 94.6%, 92.3%, 92.5%, and 87.7%, respectively. The mSEPT9 assay also had potent ability to discriminate cancer from non-cancer subjects. The combination of mSEPT9 with CEA, CA724, SNCG, or AFP significantly enhanced the sensitivity for CRC, GC, EC, and HCC to 86.4% (AUC = 0.99, specificity = 92.8%), 63.6% (AUC = 0.86, specificity = 91.1%), 71.3% (AUC = 0.81, specificity = 82.1%), and 83.3% (AUC = 0.93, specificity = 85.1%), respectively. The performance of the mSEPT9 assay was influenced by cancer stage, patient age, pathological types, and the location of cancer. We also identified that mSEPT9 was an independent risk factor and was a valuable predictor for the long-term survival of digestive cancer patients, with a hazard ratio of 2.84, 2.07, 1.88, and 2.45, for CRC, GC, EC, and HCC, respectively. CONCLUSION: The blood mSEPT9 assay, whether used alone or in combination with serum protein markers, is effective for the opportunistic screening of digestive cancers. Furthermore, mSEPT9 is an independent risk factor and a predictive marker for the long-term survival of digestive cancer patients.
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spelling pubmed-77455552021-01-04 Opportunistic screening and survival prediction of digestive cancers by the combination of blood mSEPT9 with protein markers Song, Lele Chen, Yan Gong, Yuan Wan, Jun Guo, Shaohua Liu, Hongyi Li, Yuemin Zeng, Zhen Lu, Yinying Ther Adv Med Oncol Original Research BACKGROUND: The early detection of digestive cancers and precancerous diseases remains a significant challenge. This study aimed to investigate the performance of the blood methylated SEPT9 (mSEPT9) assay, and the combination of this assay with serum protein markers, in hospital-based opportunistic screening strategies for digestive cancers. METHODS: Opportunistic screening was performed in the participating hospitals on outpatients and inpatients who met specific inclusion criteria. We recruited a total of 2030 subjects, including 764 cancer patients [291 colorectal cancer (CRC), 239 gastric cancer (GC), 106 esophageal cancer (EC), and 128 hepatocellular carcinoma (HCC)], 423 subjects with precancerous diseases, and 843 normal subjects. All samples were transported to an authenticated clinical laboratory where the mSEPT9 tests were performed. RESULTS: When used separately, the mSEPT9 detected CRC, GC, EC, and HCC, with a sensitivity of 76.6% [area under the receiver operating characteristic curve (AUC) = 0.86)], 47.7% (AUC = 0.76), 42.6% (AUC = 0.69), and 76.7% (AUC = 0.85) and a specificity of 94.6%, 92.3%, 92.5%, and 87.7%, respectively. The mSEPT9 assay also had potent ability to discriminate cancer from non-cancer subjects. The combination of mSEPT9 with CEA, CA724, SNCG, or AFP significantly enhanced the sensitivity for CRC, GC, EC, and HCC to 86.4% (AUC = 0.99, specificity = 92.8%), 63.6% (AUC = 0.86, specificity = 91.1%), 71.3% (AUC = 0.81, specificity = 82.1%), and 83.3% (AUC = 0.93, specificity = 85.1%), respectively. The performance of the mSEPT9 assay was influenced by cancer stage, patient age, pathological types, and the location of cancer. We also identified that mSEPT9 was an independent risk factor and was a valuable predictor for the long-term survival of digestive cancer patients, with a hazard ratio of 2.84, 2.07, 1.88, and 2.45, for CRC, GC, EC, and HCC, respectively. CONCLUSION: The blood mSEPT9 assay, whether used alone or in combination with serum protein markers, is effective for the opportunistic screening of digestive cancers. Furthermore, mSEPT9 is an independent risk factor and a predictive marker for the long-term survival of digestive cancer patients. SAGE Publications 2020-10-16 /pmc/articles/PMC7745555/ /pubmed/33403008 http://dx.doi.org/10.1177/1758835920962966 Text en © The Author(s), 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Song, Lele
Chen, Yan
Gong, Yuan
Wan, Jun
Guo, Shaohua
Liu, Hongyi
Li, Yuemin
Zeng, Zhen
Lu, Yinying
Opportunistic screening and survival prediction of digestive cancers by the combination of blood mSEPT9 with protein markers
title Opportunistic screening and survival prediction of digestive cancers by the combination of blood mSEPT9 with protein markers
title_full Opportunistic screening and survival prediction of digestive cancers by the combination of blood mSEPT9 with protein markers
title_fullStr Opportunistic screening and survival prediction of digestive cancers by the combination of blood mSEPT9 with protein markers
title_full_unstemmed Opportunistic screening and survival prediction of digestive cancers by the combination of blood mSEPT9 with protein markers
title_short Opportunistic screening and survival prediction of digestive cancers by the combination of blood mSEPT9 with protein markers
title_sort opportunistic screening and survival prediction of digestive cancers by the combination of blood msept9 with protein markers
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7745555/
https://www.ncbi.nlm.nih.gov/pubmed/33403008
http://dx.doi.org/10.1177/1758835920962966
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