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Feasibility of quantification based on novel evaluation with stool DNA and fecal immunochemical test for colorectal cancer detection

BACKGROUND: Stool DNA (sDNA) tests and fecal immunochemical test (FIT) are used for the detection of colorectal cancer (CRC). Here we performed a novel evaluation using sDNA and FIT to assess their performance in CRC screening and monitoring in Hubei, China. METHODS: Stool samples were collected fro...

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Autores principales: Xu, Hongli, Chen, Huixin, Hu, Junjie, Xiong, Zhiguo, Li, Dongqing, Wang, Shun, Yu, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9375944/
https://www.ncbi.nlm.nih.gov/pubmed/35963995
http://dx.doi.org/10.1186/s12876-022-02470-z
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author Xu, Hongli
Chen, Huixin
Hu, Junjie
Xiong, Zhiguo
Li, Dongqing
Wang, Shun
Yu, Jing
author_facet Xu, Hongli
Chen, Huixin
Hu, Junjie
Xiong, Zhiguo
Li, Dongqing
Wang, Shun
Yu, Jing
author_sort Xu, Hongli
collection PubMed
description BACKGROUND: Stool DNA (sDNA) tests and fecal immunochemical test (FIT) are used for the detection of colorectal cancer (CRC). Here we performed a novel evaluation using sDNA and FIT to assess their performance in CRC screening and monitoring in Hubei, China. METHODS: Stool samples were collected from a high-risk population in Hubei, China (n = 359). sDNA tests and FIT were performed to test for KRAS mutations, NDRG4 and BMP3 methylation, and check hemoglobin levels. The methylation in BMP3 and NDRG4 genes was detected by TaqMan PCR method from human fecal samples. KRAS gene mutation in human fecal DNA was tested using TaqMan probe and amplification-refractory mutation system method. The colloid gold method was used for detection of hemoglobin in fecal samples. Finally, a novel evaluation by software was used to calculate the comprehensive value of the combined results for CRC detection and monitoring. RESULTS: The sensitivity and specificity of the novel evaluation for early CRC (stage I and II), advanced adenoma (AA), and non-colon cancer neoplasm (NA) detection were 95.45% and 81.6%, 29.63% and 75.9%, and 23.08% and 75.17%, respectively. The receiver operating characteristic (ROC) curves of the combined value for the above diseases were 0.945 ± 0.015, 0.543 ± 0.055, and 0.547 ± 0.038, respectively. The levels of the novel evaluation were not significantly associated with the pathology and stage (P > 0.05). In 20 out of 22 CRC patients, the novel evaluation of sDNA and FIT had decreased below threshold (< 165) at after surgery. DISCUSSION: The novel evaluation with sDNA test and FIT has increased sensitivity for screening of CRC and AA. The novel evaluation may have potential importance as an indicator of early CRC. Additionally, the dynamic changes of the comprehensive value after surgery were correlated with CRC treatment.
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spelling pubmed-93759442022-08-15 Feasibility of quantification based on novel evaluation with stool DNA and fecal immunochemical test for colorectal cancer detection Xu, Hongli Chen, Huixin Hu, Junjie Xiong, Zhiguo Li, Dongqing Wang, Shun Yu, Jing BMC Gastroenterol Research BACKGROUND: Stool DNA (sDNA) tests and fecal immunochemical test (FIT) are used for the detection of colorectal cancer (CRC). Here we performed a novel evaluation using sDNA and FIT to assess their performance in CRC screening and monitoring in Hubei, China. METHODS: Stool samples were collected from a high-risk population in Hubei, China (n = 359). sDNA tests and FIT were performed to test for KRAS mutations, NDRG4 and BMP3 methylation, and check hemoglobin levels. The methylation in BMP3 and NDRG4 genes was detected by TaqMan PCR method from human fecal samples. KRAS gene mutation in human fecal DNA was tested using TaqMan probe and amplification-refractory mutation system method. The colloid gold method was used for detection of hemoglobin in fecal samples. Finally, a novel evaluation by software was used to calculate the comprehensive value of the combined results for CRC detection and monitoring. RESULTS: The sensitivity and specificity of the novel evaluation for early CRC (stage I and II), advanced adenoma (AA), and non-colon cancer neoplasm (NA) detection were 95.45% and 81.6%, 29.63% and 75.9%, and 23.08% and 75.17%, respectively. The receiver operating characteristic (ROC) curves of the combined value for the above diseases were 0.945 ± 0.015, 0.543 ± 0.055, and 0.547 ± 0.038, respectively. The levels of the novel evaluation were not significantly associated with the pathology and stage (P > 0.05). In 20 out of 22 CRC patients, the novel evaluation of sDNA and FIT had decreased below threshold (< 165) at after surgery. DISCUSSION: The novel evaluation with sDNA test and FIT has increased sensitivity for screening of CRC and AA. The novel evaluation may have potential importance as an indicator of early CRC. Additionally, the dynamic changes of the comprehensive value after surgery were correlated with CRC treatment. BioMed Central 2022-08-13 /pmc/articles/PMC9375944/ /pubmed/35963995 http://dx.doi.org/10.1186/s12876-022-02470-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Xu, Hongli
Chen, Huixin
Hu, Junjie
Xiong, Zhiguo
Li, Dongqing
Wang, Shun
Yu, Jing
Feasibility of quantification based on novel evaluation with stool DNA and fecal immunochemical test for colorectal cancer detection
title Feasibility of quantification based on novel evaluation with stool DNA and fecal immunochemical test for colorectal cancer detection
title_full Feasibility of quantification based on novel evaluation with stool DNA and fecal immunochemical test for colorectal cancer detection
title_fullStr Feasibility of quantification based on novel evaluation with stool DNA and fecal immunochemical test for colorectal cancer detection
title_full_unstemmed Feasibility of quantification based on novel evaluation with stool DNA and fecal immunochemical test for colorectal cancer detection
title_short Feasibility of quantification based on novel evaluation with stool DNA and fecal immunochemical test for colorectal cancer detection
title_sort feasibility of quantification based on novel evaluation with stool dna and fecal immunochemical test for colorectal cancer detection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9375944/
https://www.ncbi.nlm.nih.gov/pubmed/35963995
http://dx.doi.org/10.1186/s12876-022-02470-z
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