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Prospective evaluation of methylated SEPT9 in plasma for detection of asymptomatic colorectal cancer
BACKGROUND: As screening methods for colorectal cancer (CRC) are limited by uptake and adherence, further options are sought. A blood test might increase both, but none has yet been tested in a screening setting. OBJECTIVE: We prospectively assessed the accuracy of circulating methylated SEPT9 DNA (...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913123/ https://www.ncbi.nlm.nih.gov/pubmed/23408352 http://dx.doi.org/10.1136/gutjnl-2012-304149 |
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author | Church, Timothy Robert Wandell, Michael Lofton-Day, Catherine Mongin, Steven J Burger, Matthias Payne, Shannon R Castaños-Vélez, Esmeralda Blumenstein, Brent A Rösch, Thomas Osborn, Neal Snover, Dale Day, Robert W Ransohoff, David F |
author_facet | Church, Timothy Robert Wandell, Michael Lofton-Day, Catherine Mongin, Steven J Burger, Matthias Payne, Shannon R Castaños-Vélez, Esmeralda Blumenstein, Brent A Rösch, Thomas Osborn, Neal Snover, Dale Day, Robert W Ransohoff, David F |
author_sort | Church, Timothy Robert |
collection | PubMed |
description | BACKGROUND: As screening methods for colorectal cancer (CRC) are limited by uptake and adherence, further options are sought. A blood test might increase both, but none has yet been tested in a screening setting. OBJECTIVE: We prospectively assessed the accuracy of circulating methylated SEPT9 DNA (mSEPT9) for detecting CRC in a screening population. DESIGN: Asymptomatic individuals ≥50 years old scheduled for screening colonoscopy at 32 US and German clinics voluntarily gave blood plasma samples before colon preparation. Using a commercially available assay, three independent blinded laboratories assayed plasma DNA of all CRC cases and a stratified random sample of other subjects in duplicate real time PCRs. The primary outcomes measures were standardised for overall sensitivity and specificity estimates. RESULTS: 7941 men (45%) and women (55%), mean age 60 years, enrolled. Results from 53 CRC cases and from 1457 subjects without CRC yielded a standardised sensitivity of 48.2% (95% CI 32.4% to 63.6%; crude rate 50.9%); for CRC stages I–IV, values were 35.0%, 63.0%, 46.0% and 77.4%, respectively. Specificity was 91.5% (95% CI 89.7% to 93.1%; crude rate 91.4%). Sensitivity for advanced adenomas was low (11.2%). CONCLUSIONS: Our study using the blood based mSEPT9 test showed that CRC signal in blood can be detected in asymptomatic average risk individuals undergoing screening. However, the utility of the test for population screening for CRC will require improved sensitivity for detection of early cancers and advanced adenomas. CLINICAL TRIAL REGISTRATION NUMBER: NCT00855348 |
format | Online Article Text |
id | pubmed-3913123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-39131232014-02-05 Prospective evaluation of methylated SEPT9 in plasma for detection of asymptomatic colorectal cancer Church, Timothy Robert Wandell, Michael Lofton-Day, Catherine Mongin, Steven J Burger, Matthias Payne, Shannon R Castaños-Vélez, Esmeralda Blumenstein, Brent A Rösch, Thomas Osborn, Neal Snover, Dale Day, Robert W Ransohoff, David F Gut Colon BACKGROUND: As screening methods for colorectal cancer (CRC) are limited by uptake and adherence, further options are sought. A blood test might increase both, but none has yet been tested in a screening setting. OBJECTIVE: We prospectively assessed the accuracy of circulating methylated SEPT9 DNA (mSEPT9) for detecting CRC in a screening population. DESIGN: Asymptomatic individuals ≥50 years old scheduled for screening colonoscopy at 32 US and German clinics voluntarily gave blood plasma samples before colon preparation. Using a commercially available assay, three independent blinded laboratories assayed plasma DNA of all CRC cases and a stratified random sample of other subjects in duplicate real time PCRs. The primary outcomes measures were standardised for overall sensitivity and specificity estimates. RESULTS: 7941 men (45%) and women (55%), mean age 60 years, enrolled. Results from 53 CRC cases and from 1457 subjects without CRC yielded a standardised sensitivity of 48.2% (95% CI 32.4% to 63.6%; crude rate 50.9%); for CRC stages I–IV, values were 35.0%, 63.0%, 46.0% and 77.4%, respectively. Specificity was 91.5% (95% CI 89.7% to 93.1%; crude rate 91.4%). Sensitivity for advanced adenomas was low (11.2%). CONCLUSIONS: Our study using the blood based mSEPT9 test showed that CRC signal in blood can be detected in asymptomatic average risk individuals undergoing screening. However, the utility of the test for population screening for CRC will require improved sensitivity for detection of early cancers and advanced adenomas. CLINICAL TRIAL REGISTRATION NUMBER: NCT00855348 BMJ Publishing Group 2014-02 2013-02-13 /pmc/articles/PMC3913123/ /pubmed/23408352 http://dx.doi.org/10.1136/gutjnl-2012-304149 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Colon Church, Timothy Robert Wandell, Michael Lofton-Day, Catherine Mongin, Steven J Burger, Matthias Payne, Shannon R Castaños-Vélez, Esmeralda Blumenstein, Brent A Rösch, Thomas Osborn, Neal Snover, Dale Day, Robert W Ransohoff, David F Prospective evaluation of methylated SEPT9 in plasma for detection of asymptomatic colorectal cancer |
title | Prospective evaluation of methylated SEPT9 in plasma for detection of asymptomatic colorectal cancer |
title_full | Prospective evaluation of methylated SEPT9 in plasma for detection of asymptomatic colorectal cancer |
title_fullStr | Prospective evaluation of methylated SEPT9 in plasma for detection of asymptomatic colorectal cancer |
title_full_unstemmed | Prospective evaluation of methylated SEPT9 in plasma for detection of asymptomatic colorectal cancer |
title_short | Prospective evaluation of methylated SEPT9 in plasma for detection of asymptomatic colorectal cancer |
title_sort | prospective evaluation of methylated sept9 in plasma for detection of asymptomatic colorectal cancer |
topic | Colon |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913123/ https://www.ncbi.nlm.nih.gov/pubmed/23408352 http://dx.doi.org/10.1136/gutjnl-2012-304149 |
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