Neoplasia Diagnosis After Multi-target Stool DNA Is Enhanced Among Lowest Baseline Detectors.


Journal

Digestive diseases and sciences
ISSN: 1573-2568
Titre abrégé: Dig Dis Sci
Pays: United States
ID NLM: 7902782

Informations de publication

Date de publication:
09 2023
Historique:
received: 24 05 2023
accepted: 06 07 2023
medline: 24 8 2023
pubmed: 24 7 2023
entrez: 24 7 2023
Statut: ppublish

Résumé

Variation in colorectal neoplasia detection limits the effectiveness of screening colonoscopy. By evaluating neoplasia detection rates of individual colonoscopists, we aimed to quantify the effects of pre-procedural knowledge of a positive (+) multi-target stool DNA (mt-sDNA) on colonoscopy quality metrics. We retrospectively identified physicians who performed a high volume of + mt-sDNA colonoscopies; colorectal neoplasia at post-mt-sDNA colonoscopy was recorded. These colonoscopists were stratified into quartiles based on baseline adenoma detection rates. Baseline colonoscopy adenoma detection rates and sessile serrated lesion detection rates were compared to post-mt-sDNA colonoscopy neoplasia diagnosis rates among each quartile. Withdrawal times were measured from negative exams. During the study period (2014-17) the highest quartile of physicians by volume of post-mt-sDNA colonoscopies were evaluated. Among thirty-five gastroenterologists, their median screening colonoscopy adenoma detection rate was 32% (IQR, 28-39%) and serrated lesion detection rate was 13% (8-15%). After + mt-sDNA, adenoma diagnosis increased to 47% (36-56%) and serrated lesion diagnosis increased to 31% (17-42%) (both p < 0.0001). Median withdrawal time increased from 10 (7-13) to 12 (10-17) minutes (p < 0.0001) and was proportionate across quartiles. After + mt-sDNA, lower baseline detectors had disproportionately higher rates of adenoma diagnosis in female versus male patients (p = 0.048) and higher serrated neoplasia diagnosis rates among all patients (p = 0.0092). Knowledge of + mt-sDNA enriches neoplasia diagnosis compared to average risk screening exams. Adenomatous and serrated lesion diagnosis was magnified among those with lower adenoma detection rates. Awareness of the mt-sDNA result may increase physician attention during colonoscopy. Pre-procedure knowledge of a positive mt-sDNA test improves neoplasia diagnosis rates among colonoscopists with lower baseline adenoma detection rates, independent of withdrawal time.

Sections du résumé

BACKGROUND AND AIMS
Variation in colorectal neoplasia detection limits the effectiveness of screening colonoscopy. By evaluating neoplasia detection rates of individual colonoscopists, we aimed to quantify the effects of pre-procedural knowledge of a positive (+) multi-target stool DNA (mt-sDNA) on colonoscopy quality metrics.
METHODS
We retrospectively identified physicians who performed a high volume of + mt-sDNA colonoscopies; colorectal neoplasia at post-mt-sDNA colonoscopy was recorded. These colonoscopists were stratified into quartiles based on baseline adenoma detection rates. Baseline colonoscopy adenoma detection rates and sessile serrated lesion detection rates were compared to post-mt-sDNA colonoscopy neoplasia diagnosis rates among each quartile. Withdrawal times were measured from negative exams.
RESULTS
During the study period (2014-17) the highest quartile of physicians by volume of post-mt-sDNA colonoscopies were evaluated. Among thirty-five gastroenterologists, their median screening colonoscopy adenoma detection rate was 32% (IQR, 28-39%) and serrated lesion detection rate was 13% (8-15%). After + mt-sDNA, adenoma diagnosis increased to 47% (36-56%) and serrated lesion diagnosis increased to 31% (17-42%) (both p < 0.0001). Median withdrawal time increased from 10 (7-13) to 12 (10-17) minutes (p < 0.0001) and was proportionate across quartiles. After + mt-sDNA, lower baseline detectors had disproportionately higher rates of adenoma diagnosis in female versus male patients (p = 0.048) and higher serrated neoplasia diagnosis rates among all patients (p = 0.0092).
CONCLUSIONS
Knowledge of + mt-sDNA enriches neoplasia diagnosis compared to average risk screening exams. Adenomatous and serrated lesion diagnosis was magnified among those with lower adenoma detection rates. Awareness of the mt-sDNA result may increase physician attention during colonoscopy. Pre-procedure knowledge of a positive mt-sDNA test improves neoplasia diagnosis rates among colonoscopists with lower baseline adenoma detection rates, independent of withdrawal time.

Identifiants

pubmed: 37486445
doi: 10.1007/s10620-023-08038-5
pii: 10.1007/s10620-023-08038-5
doi:

Substances chimiques

DNA, Neoplasm 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

3721-3731

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Références

Siegel RL, Miller KD, Fuchs HE et al. Cancer statistics, 2022. CA: Cancer Journal for Clinicians 2022;72:7–33.
Davidson KW, Barry MJ, Mangione CM et al. Screening for colorectal cancer: US preventive services task force recommendation statement. Jama 2021;325:1965–1977.
doi: 10.1001/jama.2021.6238 pubmed: 34003218
Klabunde CN, Djenaba JA, King JB, White A, Plescia M. Vital signs: colorectal cancer screening test use-United States, 2012. CDC MMWR-Morbid Mortal W 2013;62:881–888.
Winawer SJ, Zauber AG, Ho MN et al. Prevention of colorectal cancer by colonoscopic polypectomy. The national polyp study workgroup. The New England Journal of Medicine 1993;329:1977–1981.
doi: 10.1056/NEJM199312303292701 pubmed: 8247072
Barclay RL, Vicari JJ, Doughty AS et al. Colonoscopic withdrawal times and adenoma detection during screening colonoscopy. N Engl J Med 2006;355:2533–2541.
doi: 10.1056/NEJMoa055498 pubmed: 17167136
Chen SC, Rex DK. Endoscopist can be more powerful than age and male gender in predicting adenoma detection at colonoscopy. Am J Gastroenterol 2007;102:856–861.
doi: 10.1111/j.1572-0241.2006.01054.x pubmed: 17222317
Barclay RL, Vicari JJ, Doughty AS et al. Serrated and adenomatous polyp detection increases with longer withdrawal time: results from the New Hampshire Colonoscopy Registry. Am J Gastroenterol 2014;109:417–426.
doi: 10.1038/ajg.2013.442
Corley DA, Jensen CD, Marks AR et al. Adenoma detection rate and risk of colorectal cancer and death. New England Journal of Medicine 2014;370:1298–1306.
doi: 10.1056/NEJMoa1309086 pubmed: 24693890
Kaminski MF, Regula J, Kraszewska E et al. Quality indicators for colonoscopy and the risk of interval cancer. New England Journal of Medicine 2010;362:1795–1803.
doi: 10.1056/NEJMoa0907667 pubmed: 20463339
Stegmaier C, Brenner H, Altenhofen L et al. Protection from right- and left-sided colorectal neoplasms after colonoscopy: population-based study. JNCI: Journal of the National Cancer Institute. 2010;102:89–95.
doi: 10.1093/jnci/djp436 pubmed: 20042716
Baxter NN, Warren JL, Barrett MJ et al. Association between colonoscopy and colorectal cancer mortality in a US cohort according to site of cancer and colonoscopist specialty. Journal of Clinical Oncology: Official Journal of the American Society of Clinical Oncology 2012;30:2664–9.
doi: 10.1200/JCO.2011.40.4772 pubmed: 22689809
Nishihara R, Wu K, Lochhead P et al. Long-term colorectal-cancer incidence and mortality after lower endoscopy. The New England journal of medicine. 2013;369:1095–1105.
doi: 10.1056/NEJMoa1301969 pubmed: 24047059
Kim SY, Lee SJ, Chung JW et al. Efficacy of repeat forward-view examination of the right-sided colon during colonoscopy: A prospective randomized controlled trial. J Gastroenterol Hepatol. 2020. https://doi.org/10.1111/jgh.15064 .
doi: 10.1111/jgh.15064 pubmed: 33217054 pmcid: 7818190
Cubiella J, Castells A, Andreu M et al. Correlation between adenoma detection rate in colonoscopy- and fecal immunochemical testing-based colorectal cancer screening programs. United European Gastroenterology Journal 2017;5:255–60.
doi: 10.1177/2050640616660662 pubmed: 28344793
Robertson DJ, Lee JK, Boland CR et al. Recommendations on fecal immunochemical testing to screen for colorectal neoplasia: a consensus statement by the US multi-society task force on colorectal cancer. Gastroenterology 2017;152:1217–37.e3.
doi: 10.1053/j.gastro.2016.08.053 pubmed: 27769517
Kligman E, Li W, Eckert GJ et al. Adenoma detection rate in asymptomatic patients with positive fecal immunochemical tests. Digestive Diseases and Sciences 2018;63:1167–72.
doi: 10.1007/s10620-018-4984-9
Anderson JC, Robinson CM, Hisey W et al. Colonoscopy findings in FIT+ and mt-sDNA+ patients versus in colonoscopy-only patients: new hampshire colonoscopy registry data. Cancer Prev Res (Phila). 2022;15:455–64.
doi: 10.1158/1940-6207.CAPR-21-0581 pubmed: 35378546 pmcid: 9662869
Imperiale TF, Ransohoff DF, Itzkowitz SH et al. Multitarget stool DNA testing for colorectal-cancer screening. New England Journal of Medicine 2014;370:1287–97.
doi: 10.1056/NEJMoa1311194 pubmed: 24645800
Johnson DH, Kisiel JB, Burger KN et al. Multitarget stool DNA test: clinical performance and impact on yield and quality of colonoscopy for colorectal cancer screening. Gastrointest Endosc 2017;85:657-665.e1.
doi: 10.1016/j.gie.2016.11.012 pubmed: 27884518
Eckmann JD, Ebner DW, Bering J et al. Multitarget stool DNA screening in clinical practice: high positive predictive value for colorectal neoplasia regardless of exposure to previous colonoscopy. Am J Gastroenterol 2020;115:608–615.
doi: 10.14309/ajg.0000000000000546 pubmed: 32068535 pmcid: 7127971
Gupta S, Lieberman D, Anderson JC et al. Recommendations for follow-up after colonoscopy and polypectomy: a consensus update by the us multi-society task force on colorectal cancer. Official Journal of the American College of Gastroenterology/ACG 2020;115:415–34.
doi: 10.14309/ajg.0000000000000544
Ezaz G, Leffler DA, Beach S et al. Association between endoscopist personality and rate of adenoma detection. Clin Gastroenterol Hepatol 2019;17:1571-1579.e7.
doi: 10.1016/j.cgh.2018.10.019 pubmed: 30326300
Dik VK et al. Measuring gaze patterns during colonoscopy: a useful tool to evaluate colon inspection? European Journal of Gastroenterology & Hepatology 2016;28:1400–1406.
doi: 10.1097/MEG.0000000000000717
Mehrotra A, Morris M, Gourevitch RA et al. Physician characteristics associated with higher adenoma detection rate. Gastrointest Endosc 2018;87:778-786.e5.
doi: 10.1016/j.gie.2017.08.023 pubmed: 28866456
Rex DK, Ahnen DJ, Baron JA et al. Serrated lesions of the colorectum: review and recommendations from an expert panel. Official Journal of the American College of Gastroenterology/ACG 2012;107:1315–29.
doi: 10.1038/ajg.2012.161
Wong JCT, Chiu HM, Kim HS et al. Adenoma detection rates in colonoscopies for positive fecal immunochemical tests versus direct screening colonoscopies. Gastrointestinal Endoscopy 2019;89:607-613.e1.
doi: 10.1016/j.gie.2018.11.014 pubmed: 30452915
Chang L-C, Shun C-T, Hsu W-F et al. Fecal immunochemical test detects sessile serrated adenomas and polyps with a low level of sensitivity. Clinical Gastroenterology and Hepatology 2017;15:872-879.e1.
doi: 10.1016/j.cgh.2016.07.029 pubmed: 27498176
Bosch LJW, Melotte V, Mongera S et al. Multitarget stool DNA test performance in an average-risk colorectal cancer screening population. Am J Gastroenterol 2019;114:1909–1918.
doi: 10.14309/ajg.0000000000000445 pubmed: 31764091 pmcid: 6903367
van Toledo D, Jeg IJ, Bossuyt PMM et al. Serrated polyp detection and risk of interval post-colonoscopy colorectal cancer: a population-based study. Lancet Gastroenterol Hepatol 2022;7:747–54.
doi: 10.1016/S2468-1253(22)00090-5 pubmed: 35550250
Anderson JC, Hisey WM, Robinson CM et al. Serrated polyp yield at colonoscopy in patients with positive FIT, positive mt-sDNA, and colonoscopy only: data from the new hampshire colonoscopy registry. Cancer Epidemiol Biomarkers Prev 2023;32:226–232.
doi: 10.1158/1055-9965.EPI-22-0527 pubmed: 36409472
Kahi CJ, Li X, Eckert GJ et al. High colonoscopic prevalence of proximal colon serrated polyps in average-risk men and women. Gastrointestinal Endoscopy 2012;75:515–520.
doi: 10.1016/j.gie.2011.08.021 pubmed: 22018551
Rex DK, Schoenfeld PS, Cohen J et al. Quality indicators for colonoscopy. Gastrointestinal Endoscopy 2015;81:31–53.
doi: 10.1016/j.gie.2014.07.058 pubmed: 25480100
A Ahlquist D. Aberrantly methylated gene marker levels in stool: effects of demographic, exposure, body mass, and other patient characteristics. Journal of Molecular Biomarkers & Diagnosis. 2012. https://doi.org/10.4172/2155-9929.1000133 .
doi: 10.4172/2155-9929.1000133

Auteurs

Derek W Ebner (DW)

Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

Kelli N Burger (KN)

Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

Douglas W Mahoney (DW)

Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

Brendan T Broderick (BT)

Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

Jason D Eckmann (JD)

Division of Gastroenterology, Hepatology, and Nutrition, University of Minnesota, Minneapolis, MN, USA.

Mary E Devens (ME)

Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

Kari L Lowrie (KL)

Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

John B League (JB)

Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

Jamie Bering (J)

Mayo Clinic, Scottsdale, AZ, USA.

Allon Kahn (A)

Mayo Clinic, Scottsdale, AZ, USA.

Eduardo A Rodriguez (EA)

Division of Gastroenterology, Hepatology and Nutrition, University of Utah, Salt Lake City, UT, USA.

David O Prichard (DO)

Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

Michael B Wallace (MB)

Mayo Clinic, Jacksonville, FL, USA.

Sunanda V Kane (SV)

Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

Jonathan A Leighton (JA)

Mayo Clinic, Scottsdale, AZ, USA.

Navtej S Buttar (NS)

Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

Lila J Finney Rutten (LJF)

Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

Suryakanth R Gurudu (SR)

Mayo Clinic, Scottsdale, AZ, USA.

John B Kisiel (JB)

Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA. kisiel.john@mayo.edu.

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